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Abels, C
Differenzial diagnosis of acute encephalopathy: Acute decompensation in ornithine transcarbamylase (OTC) deficiency in a seven year old girl
Adler, C
Therapy of Hemiparesis in children and adolescents – a 5 years experience
Agaimy, A
Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation
Ahting, U
Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation
Biochemical and genetic testing in a large cohort of patients with suspicion of mitochondriopathy
Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients
Aktas, M
MRI signal changes of the brain stem in children with infantile spasms are not a side effect of vigabatrin therapy
Alber, M
Comparison of different tractography algorithms and validation by intraoperative stimulation in a child with a brain tumor
Alberg, E
SelenoproteinN1-related myopathy: From clinical signs to diagnosis
Albrecht, U
Unrecognized citrullinemia mimicking encephalitis in a 14 year-old boy – the role of a standardized lumbar puncture protocol
Antonius-Kluger, E
Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy
Aslami, B
Multileveltherapy with botulinumtoxin A in children with cerebral movement disorders
Axer, S
Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009
Backes, H
Multileveltherapy with botulinumtoxin A in children with cerebral movement disorders
Baethmann, M
Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine
Neuroborreliosis with cerebrovascular disease causes ischemic stroke in a 12 year old boy
Longitudinally very extensive acute transverse myelitis after influenza vaccination
Banwell, B
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Barkmann, C
Psychopathology in CLN3 disease: Correlation with disease progression and quality of life
Bar-Or, A
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Basheer, N
High incidence of paediatric CNS demyelination in East London
Bast, T
Modified Atkins diet as a treatment of epilepsy in 23 children
Neuropsychological and social functions in children and adoloescents with hypothalamic harmatomas
Resective surgery for refractory epilepsy in children under 4 years of age
Efficacy and safety of oral lacosamide as adjunctive therapy in children under 16 years with partial-onset seizures
Bauer, A
Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences
Bauer, J
Neurocognitive deficits in children requiring heart transplantation during infancy
Bauer, M
PDH deficiency: identification of a novel mutation in the PDHA1gene in twins with intermittent weakness, resembling Guillain-Barré syndrome
Baumann, M
Suspected bromide intoxication due to ketogenic diet?
Baumann, U
Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation
Baumgartner-Sigl, S
Suspected bromide intoxication due to ketogenic diet?
Bechtold-Dalla Pozza, S
Vitamin D levels in pediatric Multiple Sclerosis patients
Beck, J
A vanishing cerebellar tumor – too good to be true
Beck, M
The new Gaucher-Pass: A key tool in management of shortage
Becker, H
AWMF-Guideline developmental coodination disorder: definition and assessment
AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention
Behnke-Hall, K
Neurocognitive deficits in children requiring heart transplantation during infancy
Behrends, U
Multiple ischemic strokes in a case of Transient Cerebral Arteriopathy (TCA) following chickenpox
Behrens, A
Spine fracture following generalized tonic-clonic seizures in a 16 years old girl. An unusual case
Benninger, F
Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study
Bentele, KHP
Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences
Berger, A
A case of familial Labrune syndrome
Berger, C
Constraint-induced movement therapy versus bimanual therapy for children with central hemiparesis – relative effectiveness and factors of influence
Bernhard, M
Successful bevacizumab therapy for CNS radiation necrosis after stereotactic radiotherapy of an arteriovenous malformation
Pyruvate dehydrogenase deficiency presenting as Guillain-Barré syndrome
Bernhard, MK
TENS therapy in tension headaches – little helps much?!
Emotional lability as a leading symptom of tetrasomy 18p in a 7-year-old girl with developmental delay, hypertonus of the adductors, kyphosis and facial anomalies
Myoclonus, ataxia and dancing eyes – visual diagnosis with diverse phenotype. Two cases of Opsoclonus-Myoclonus-Syndrome after adenoviral infection and scarlet fever
Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus
Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex
Bernius, P
CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort
Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results
Bertsche, A
Modification of epileptiform activity by blocking glial glutamate uptake
Berweck, S
A four day course of Lovastatin improves synaptic plasticity in patients with NF-1
CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort
Therapy of Hemiparesis in children and adolescents – a 5 years experience
Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept
Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results
The application of the German hip surveillance protocol in children with bilateral spastic cerebral palsy – a single centre cohort study
Usefulness of RemiPro for pediatric neurorehabilitation in severe head injury: A case report
Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy
Betz, N
Modified Atkins diet as a treatment of epilepsy in 23 children
Bevot, A
Selective dorsal rhizotomy – selection criteria and outcome in the frst year after a new etablished invasive treatment
Patients with neuromuscular scoliosis after spinal fusion and instrumentation: clinical, radiometric and functional results
Beyerlein, A
CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort
Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results
Bigi, S
Acquired isolated focal cerebellar lesions during development: effect on cognition?
Biskup, S
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Biste, M
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients
Bittner, R
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Blank, AE
Fluid accumulation in the fetal extracerebral spaces: External hydrocephalus or subdural hygromas?
Blank, R
AWMF-Guideline developmental coodination disorder: definition and assessment
AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention
Blankenburg, U
Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy
Blaschek, A
Anti-NMDAR Encephalitis in children: Delineation of the epileptic phenotypes
Disturbances of the vestibular and ocular motor systems in children with demyelinisating disorders of the central nervous system
Vitamin D levels in pediatric Multiple Sclerosis patients
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Bluemcke, I
"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis
Blümcke, I
Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions
Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection
Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients
Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion
Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy
12 years of pediatric epilepsy surgery – The Vogtareuth experience
Bodamer, O
Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening
Bode, H
Cerebral palsy: Predictors of psychosocial development
Böhmer, J
Migraine – the chameleon of diseases
Bohring, A
Potocki-Shaffer Syndrome: A case study
Boltshauser, E
Phacomatosis pigmentovascularis and extensive venous malformation of brain vessels. A unknown association or a new vascular neurocutaneous syndrome?
Acquired isolated focal cerebellar lesions during development: effect on cognition?
Postnatal in-vivo MRI findings in anencephaly
Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients
Boor, R
Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome
Borggraefe, I
Online EEG analysis by an epilepsy center
Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept
Borggräfe, I
Anti-NMDAR Encephalitis in children: Delineation of the epileptic phenotypes
DYT 11 Myoclonus-Dystonia Syndrome (MDS) with generalized epileptic discharges
Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?
Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy
Brackmann, F
Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation
Brandl, U
The role of sharp wave activity in the consolidation of learning during sleep
Brandt, A
A four day course of Lovastatin improves synaptic plasticity in patients with NF-1
Brassel, F
Spine fracture following generalized tonic-clonic seizures in a 16 years old girl. An unusual case
Brehm, M
Cognitve impairment as a leading symptom in juvenile MS – two case reports -
Breithaupt, C
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Breiting, M
Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy
Breuer, U
Therapy of Hemiparesis in children and adolescents – a 5 years experience
Brilot, F
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Brix, O
CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort
Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results
Brixius-Huth, M
The new Gaucher-Pass: A key tool in management of shortage
Brocke, K
Reference intervals of plasma catecholamines in newborns for diagnosis of Menkes disease
A case of sudden cardiac death in a patient with LPIN1 gene mutation
Bruehl, C
Modification of epileptiform activity by blocking glial glutamate uptake
Brunner-Krainz, M
Multiple arteriovenous malformations of the brain: A case report
Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: discussion of different phenotypes in two pediatric patients
Büchel, A
Optic nerve sheath diameter by ultrasound in children and adolescents with headache
Buchmann, A
Morphometric MRI findings in adolescents with congenital heart disease
Bültmann, E
Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation
Burdach, S
Multiple ischemic strokes in a case of Transient Cerebral Arteriopathy (TCA) following chickenpox
Treatment of severe childhood Multiple Sclerosis with plasmapheresis
Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum
Burtzlaff, C
Drug resistant seizures at the age of 3 months – mild form of a non-ketotic hyperglycinemia (NKH)
Stiff-persons syndrome in a 12 year old child – a case report
Busse, M
Ataxia telangiectasia in dizygotic two year old twins
Bussmann, CB
Oculocutaneous albinism
Bußmann, C
PDH deficiency: identification of a novel mutation in the PDHA1gene in twins with intermittent weakness, resembling Guillain-Barré syndrome
Christen, HJ
Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation
Clas, P
Semi-Automatic quantification of demyelination load in children with metachromatic leukodystrophy on MR-images
Coppola, G
First observations of treatment with rufinamide in children with myoclonic-astatic epilepsy
Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome
Crow, YJ
A case of familial Labrune syndrome
Csaicsich, D
Early plasmapheresis in 3 consecutive cases of choreo-athetotic movement disorder after HSV-1 encephalitis
Czermin, B
Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation
Dahlin, M
Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome
Dale, RC
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Danhauser, K
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Das, AM
Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation
Dechant, K
First experience of a parents questionnaire to define therapeutic goals for ketogenic diet in children with difficult-to-treat epilepsy
Deiters, L
Development of pretems <1500g in the first two years of life: Standardized testing according to the Griffith Scales and Mental Bayley Scales
Delalande, O
Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion
de Lonlay, P
A case of sudden cardiac death in a patient with LPIN1 gene mutation
Delvendahl, I
A four day course of Lovastatin improves synaptic plasticity in patients with NF-1
Denecke, J
Kleine-Levin syndrome: a disorder with recurring hypersomnia as main symptom
Familial occurence of congenital bilateral perisylvian syndrom
Deppe, W
Constraint-induced movement therapy versus bimanual therapy for children with central hemiparesis – relative effectiveness and factors of influence
Derfuß, T
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
der Hagen, M von
A case of sudden cardiac death in a patient with LPIN1 gene mutation
Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy
Diepold, K
Late-onset folinic acid-responsive seizures
Dikow, N
Cohen syndrome – an important differenzial diagnosis for children with mental retardation and secondary microcephaly
Distelmaier, F
How do we sedate children undergoing CSF opening pressure measurement? Results of a Germany-wide survey
Dornmair, K
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Draguhn, A
Modification of epileptiform activity by blocking glial glutamate uptake
Dressel, P
Neurological presentations in children with serological active mycoplasma pneumoniae infection
Dressler, A
Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study
Eberhard, C
Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy
Ebner, A
Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009
Ebner, K
Analysis of the control condition of a language fMRI task: a simple alternative to assess visuospatial functions?
Eder, HG
Multiple arteriovenous malformations of the brain: A case report
Eisenhofer, G
Reference intervals of plasma catecholamines in newborns for diagnosis of Menkes disease
Eitel, H
Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions
Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection
Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome
Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion
"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis
12 years of pediatric epilepsy surgery – The Vogtareuth experience
Eitel, HC
Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients
Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy
First experience of a parents questionnaire to define therapeutic goals for ketogenic diet in children with difficult-to-treat epilepsy
Elger, CE
A method for automated volumetry to assess disease progression in Rasmussen Encephalitis
Elix, H
Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex
Elsenbruch, S
Health- related quality of life in patients with Duchenne Muscular Dystrophy
Elstner, M
Identification of a second major locus for neurodegeneration with brain iron accumulation
Engelsberger, I
Longitudinally very extensive acute transverse myelitis after influenza vaccination
Ensslen, M
Anti-NMDAR Encephalitis in children: Delineation of the epileptic phenotypes
Eves, K
The treatment of young children with low trunkal tone, as a result of various diagnoses, with dynamic GPS Soft Orthoses – case studies
Faber, J
Isolated, monocular vertical nystagmus: single symptom of an extensive intracerebral tumor
Feldkamp, A
Complete occlusion of the left internal carotid artery in neurofibromatosis type 1. Congenital dysplasia or progressive occlusion?
Feucht, M
Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study
Fiedler, B
Differenzial diagnosis of acute encephalopathy: Acute decompensation in ornithine transcarbamylase (OTC) deficiency in a seven year old girl
Hereditary sensory and autonomic neuropathy Type IV – a case report with detection of two previously unknown sequence variants in NTKR1 gene
Fiedler, BJ
Potocki-Shaffer Syndrome: A case study
Finetti, C
Spine fracture following generalized tonic-clonic seizures in a 16 years old girl. An unusual case
Complete occlusion of the left internal carotid artery in neurofibromatosis type 1. Congenital dysplasia or progressive occlusion?
Fingerhut, M
Status epilepticus in a newborn – pyridoxine toxicity?
Fleischer, J
Constraint-induced movement therapy versus bimanual therapy for children with central hemiparesis – relative effectiveness and factors of influence
Flössel, U
A case of sudden cardiac death in a patient with LPIN1 gene mutation
Forne, I
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Fowler, B
Infantile epileptic encephalopathy due to cobalamin deficiency?
Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine
Franke, C
Treatment of severe childhood Multiple Sclerosis with plasmapheresis
Frauenknecht, K
Isolated, monocular vertical nystagmus: single symptom of an extensive intracerebral tumor
Freilinger, M
Early plasmapheresis in 3 consecutive cases of choreo-athetotic movement disorder after HSV-1 encephalitis
Freisinger, P
Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation
Deficiency of the mitochondrial phosphate carrier as a cause of combined mitochondrial (cardio-)myopathy
Biochemical and genetic testing in a large cohort of patients with suspicion of mitochondriopathy
Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients
Freudenberg, L
A four day course of Lovastatin improves synaptic plasticity in patients with NF-1
Gabriel, H
Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation
Gangfuß, A
Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)
Garkisch, S
PCDH19 defects in girls with infantile myoclonic epilepsy with and without autism
Gärtner, J
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Gassmann, M
Activation of neuronal migration factor CXCR4 by pharmacological HIF stabilization in developing mouse brain
Gebhardt, B
Optic nerve sheath diameter by ultrasound in children and adolescents with headache
Geers, B
Health- related quality of life in patients with Duchenne Muscular Dystrophy
Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)
Geiger, K
A case of sudden cardiac death in a patient with LPIN1 gene mutation
Geis, T
An unusual tremor
A patient with mutations in the dystrophin and the FKRP gene – „double trouble“ or incidental finding
Gencik, M
Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation
Gerleve, H
The effect of Lamotrigin and Levetiracetam on the perinatal period
Encephalitis of varizella-zoster in a 26 months old child
Gerstner, T
Resective surgery for refractory epilepsy in children under 4 years of age
Getzinger, T
Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection
Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients
Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion
"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis
Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy
12 years of pediatric epilepsy surgery – The Vogtareuth experience
Geuze, R
AWMF-Guideline developmental coodination disorder: definition and assessment
Goeggel Simonetti, B
A vanishing cerebellar tumor – too good to be true
Gold, R
Optical Coherence Tomography in neuro-pediatric diseases – A case report
Goll, A
Patients with neuromuscular scoliosis after spinal fusion and instrumentation: clinical, radiometric and functional results
Grohmann, K
Drug resistant seizures at the age of 3 months – mild form of a non-ketotic hyperglycinemia (NKH)
Gröschel, S
Semi-Automatic quantification of demyelination load in children with metachromatic leukodystrophy on MR-images
Comparison of different tractography algorithms and validation by intraoperative stimulation in a child with a brain tumor
Grossmann, R
DYT 11 Myoclonus-Dystonia Syndrome (MDS) with generalized epileptic discharges
Gruber-Sedlmayr, U
Multiple arteriovenous malformations of the brain: A case report
Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: discussion of different phenotypes in two pediatric patients
Gushahn, L
Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy
Haack, T
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients
Identification of a second major locus for neurodegeneration with brain iron accumulation
Haack, TB
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Habelt, C
Longitudinally very extensive acute transverse myelitis after influenza vaccination
Haberberger, B
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Haberlandt, E
Unrecognized citrullinemia mimicking encephalitis in a 14 year-old boy – the role of a standardized lumbar puncture protocol
Suspected bromide intoxication due to ketogenic diet?
Häberle, J
Unrecognized citrullinemia mimicking encephalitis in a 14 year-old boy – the role of a standardized lumbar puncture protocol
Haffner, D
Kleine-Levin syndrome: a disorder with recurring hypersomnia as main symptom
Familial occurence of congenital bilateral perisylvian syndrom
Hahn, A
PCDH19 defects in girls with infantile myoclonic epilepsy with and without autism
Neurocognitive deficits in children requiring heart transplantation during infancy
Postanoxic myoclonus (Lance-Adams syndrome) after near-drowning
Hannibal, I
DYT 11 Myoclonus-Dystonia Syndrome (MDS) with generalized epileptic discharges
Hans, V
Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009
Harter, PN
Fluid accumulation in the fetal extracerebral spaces: External hydrocephalus or subdural hygromas?
Hartig, MB
Identification of a second major locus for neurodegeneration with brain iron accumulation
Härtig, W
Myoclonus, ataxia and dancing eyes – visual diagnosis with diverse phenotype. Two cases of Opsoclonus-Myoclonus-Syndrome after adenoviral infection and scarlet fever
Hartlieb, T
Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection
Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients
Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion
"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis
Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy
12 years of pediatric epilepsy surgery – The Vogtareuth experience
Hartmann, H
Status epilepticus in a newborn – pyridoxine toxicity?
Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation
Hartmann, M
Psychopathology in CLN3 disease: Correlation with disease progression and quality of life
Hasilik, M
Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences
Hauffa, B
Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)
Haug, V
Isolated, monocular vertical nystagmus: single symptom of an extensive intracerebral tumor
Hauser, TK
Analysis of the control condition of a language fMRI task: a simple alternative to assess visuospatial functions?
Häusler, M
MRI signal changes of the brain stem in children with infantile spasms are not a side effect of vigabatrin therapy
Rufinamide. A new therapeutic option for epilepsy with myoclonic absences
Heidrich, A
The new Gaucher-Pass: A key tool in management of shortage
Heim, K
Identification of a second major locus for neurodegeneration with brain iron accumulation
Heinen, F
Online EEG analysis by an epilepsy center
Anti-NMDAR Encephalitis in children: Delineation of the epileptic phenotypes
DYT 11 Myoclonus-Dystonia Syndrome (MDS) with generalized epileptic discharges
A four day course of Lovastatin improves synaptic plasticity in patients with NF-1
Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept
Standardized and validated evaluation of groß motor function of children with cerebral palsy: Establishment of the Gross Motor Function Measure in German speaking countries
Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?
Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy
The application of the German hip surveillance protocol in children with bilateral spastic cerebral palsy – a single centre cohort study
Abstracts of the 37th Annual Meeting of the Society of – Neuropediatrics, „Gesellschaft für Neuropädiatrie“ – 7nd to 10th April 2011
Disturbances of the vestibular and ocular motor systems in children with demyelinisating disorders of the central nervous system
Vitamin D levels in pediatric Multiple Sclerosis patients
Heiniger, U
Ongoing improvement in mobility, activity and cognition of a teenage girl with pediatric multiple sclerosis after 3 years of natalizumab treatment – a case report
Heinks-Maldonado, T
Acquired isolated focal cerebellar lesions during development: effect on cognition?
Heinrich, M
Familiarity and course of specific language impairment of 175 children
Heinrich, T
Fluid accumulation in the fetal extracerebral spaces: External hydrocephalus or subdural hygromas?
Hemmer, B
Treatment of severe childhood Multiple Sclerosis with plasmapheresis
Hempel, M
Familiarity and course of specific language impairment of 175 children
Identification of a second major locus for neurodegeneration with brain iron accumulation
Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum
Henrich, M
Ataxia telangiectasia in dizygotic two year old twins
Herberhold, TM
Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences
Herraiz Rocamora, J
Inv dup (15) syndrome and refractory epilepsy: A case-report
Hessel, A
Robotic-assisted gait training improves gait parameters and functional mobility in patients wit cerebral palsy – preliminary results
Hessenauer, M
Therapy of Hemiparesis in children and adolescents – a 5 years experience
Usefulness of RemiPro for pediatric neurorehabilitation in severe head injury: A case report
Heußinger, N
Isolated optic neuritis is associated with development of pediatric multiple sclerosis
Hiener, U
Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine
Neuroborreliosis with cerebrovascular disease causes ischemic stroke in a 12 year old boy
Longitudinally very extensive acute transverse myelitis after influenza vaccination
Himpel, M
TENS therapy in tension headaches – little helps much?!
Hinterstoißer, K
Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept
The application of the German hip surveillance protocol in children with bilateral spastic cerebral palsy – a single centre cohort study
Hinz, AB
Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia
Hirsch, W
Successful bevacizumab therapy for CNS radiation necrosis after stereotactic radiotherapy of an arteriovenous malformation
Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus
Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex
Hirzinger, M
Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy
Hoffmann, GF
Therapeutic modulation of cerebral lysine metabolism in a mouse model for glutaric aciduria type I
Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia
Hofmann, W
Biochemical and genetic testing in a large cohort of patients with suspicion of mitochondriopathy
Hohlfeld, R
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Holert, N
Isolated corpus callosum agenesis as a rare differenzial diagnosis of attention defficit hyperactivity disorder- case report
Holinski-Feder, E
Hereditary sensory and autonomic neuropathy Type IV – a case report with detection of two previously unknown sequence variants in NTKR1 gene
Holthausen, H
Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions
Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection
Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome
Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients
Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion
"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis
Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy
12 years of pediatric epilepsy surgery – The Vogtareuth experience
Reoperations and second step-procedures in pediatric epilepsy surgery – indications, new techniques, limitations and results
Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome
Homburg, MC
Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?
Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy
Honnef, D
MRI signal changes of the brain stem in children with infantile spasms are not a side effect of vigabatrin therapy
Hoppen, T
Reversible hepatopathy during beta-interferone therapy of Multiple Sclerosis
Hörster, F
Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia
Horvat, R
Deficiency of the mitochondrial phosphate carrier as a cause of combined mitochondrial (cardio-)myopathy
Horvath, R
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients
Hoser, J
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Huber, R
Qualitative and quantitative motor performance in adolescents with CHD
Hübner, A
Reference intervals of plasma catecholamines in newborns for diagnosis of Menkes disease
A case of sudden cardiac death in a patient with LPIN1 gene mutation
Huisman, TAGM
Postnatal in-vivo MRI findings in anencephaly
Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients
Hume, R
Reference intervals of plasma catecholamines in newborns for diagnosis of Menkes disease
Hung, C
Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening
Huppke, P
Reversible hepatopathy during beta-interferone therapy of Multiple Sclerosis
Huß, K
DYT 11 Myoclonus-Dystonia Syndrome (MDS) with generalized epileptic discharges
Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept
Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?
Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy
The application of the German hip surveillance protocol in children with bilateral spastic cerebral palsy – a single centre cohort study
Hütsch, C
Robotic-assisted gait training improves gait parameters and functional mobility in patients wit cerebral palsy – preliminary results
Specific motion patterns of the sagittal, frontal and transversal plane in children with bilateral spastic cerebral palsy: Preliminary results of a cross-sectional study
Illsinger, S
Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation
Iuso, A
Identification of a second major locus for neurodegeneration with brain iron accumulation
Jacob, U
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Jakobs, C
Status epilepticus in a newborn – pyridoxine toxicity?
Janello, C
Urolithiasis with Topiramate and Zonisamide: Therapy? Prophylaxis?
Janetschek, C
Suspected bromide intoxication due to ketogenic diet?
Jansen, C
Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept
The application of the German hip surveillance protocol in children with bilateral spastic cerebral palsy – a single centre cohort study
Jenne, D
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Jenni, O
AWMF-Guideline developmental coodination disorder: definition and assessment
AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention
Jozwiak, S
Identification of a second major locus for neurodegeneration with brain iron accumulation
Jung, N
A four day course of Lovastatin improves synaptic plasticity in patients with NF-1
CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort
Jung, NH
Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results
Jurkiewicz, E
Identification of a second major locus for neurodegeneration with brain iron accumulation
Kalbhenn, T
Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009
Kalle, T von
Tumefactive demyelinating lesion – a rare manifestation of multiple sclerosis in childhood
Kalmus, U
The effect of Lamotrigin and Levetiracetam on the perinatal period
Stimulus-sensitive epilepsy, with seizures while feeding in the morning
Encephalitis of varizella-zoster in a 26 months old child
Käppeli, M
Ongoing improvement in mobility, activity and cognition of a teenage girl with pediatric multiple sclerosis after 3 years of natalizumab treatment – a case report
Karall, D
Unrecognized citrullinemia mimicking encephalitis in a 14 year-old boy – the role of a standardized lumbar puncture protocol
Suspected bromide intoxication due to ketogenic diet?
Karch, S
Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia
Cohen syndrome – an important differenzial diagnosis for children with mental retardation and secondary microcephaly
Karenfort, M
Childhood arterial ischemic stroke related to anabolic steroid and cannabis abuse
Crossed cerebellar diaschisis after status epilepticus
Karlmeier, A
12 years of pediatric epilepsy surgery – The Vogtareuth experience
Keimer, R
Tumefactive demyelinating lesion – a rare manifestation of multiple sclerosis in childhood
Kennerknecht, I
Hereditary prosopagnosia
Kessler, S
Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome
Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients
Kessler-Uberti, S
Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions
Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection
"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis
Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy
Keßler-Uberti, S
Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion
12 years of pediatric epilepsy surgery – The Vogtareuth experience
Reoperations and second step-procedures in pediatric epilepsy surgery – indications, new techniques, limitations and results
Keßner, R
Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy
Khademi, M
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Kiechl-Kohlendorfer, U
Old and new antiepileptic drugs during pregnancy and lactation – report of a case
Kiefer, A
Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation
Kiess, W
Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex
Kilian, D
Psychopathology in CLN3 disease: Correlation with disease progression and quality of life
Kirchhoff, F
Kleine-Levin syndrome: a disorder with recurring hypersomnia as main symptom
Kirsch, S
Tumefactive demyelinating lesion – a rare manifestation of multiple sclerosis in childhood
Kissenbeck, C
Psychopathology in CLN3 disease: Correlation with disease progression and quality of life
Klaver, P
Qualitative and quantitative motor performance in adolescents with CHD
Morphometric MRI findings in adolescents with congenital heart disease
Klee, D
Crossed cerebellar diaschisis after status epilepticus
Klein, C
Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia
Klein, GE
Multiple arteriovenous malformations of the brain: A case report
Klepper, J
20 years of GLUT1 Deficiency: where are we today?
Klopstock, T
Identification of a second major locus for neurodegeneration with brain iron accumulation
Kluger, G
Urolithiasis with Topiramate and Zonisamide: Therapy? Prophylaxis?
CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort
Usefulness of RemiPro for pediatric neurorehabilitation in severe head injury: A case report
Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy
First observations of treatment with rufinamide in children with myoclonic-astatic epilepsy
Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome
Rufinamide. A new therapeutic option for epilepsy with myoclonic absences
First experience of a parents questionnaire to define therapeutic goals for ketogenic diet in children with difficult-to-treat epilepsy
Kmiec, T
Identification of a second major locus for neurodegeneration with brain iron accumulation
Knirsch, W
Morphometric MRI findings in adolescents with congenital heart disease
Koch, J
Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening
Koch, K
Cohen syndrome – an important differenzial diagnosis for children with mental retardation and secondary microcephaly
Koch, KA
Oculocutaneous albinism
Koehler, T
Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results
Koeller, DM
Therapeutic modulation of cerebral lysine metabolism in a mouse model for glutaric aciduria type I
Kohleis, K
Cerebral palsy: Predictors of psychosocial development
Köhler, C
Dissociative gait disturbance versus Guillain-Barré-Syndrom -pitfalls in clinical presentation and diagnostics
Kohlhase, J
Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia
Kohlschütter, A
Psychopathology in CLN3 disease: Correlation with disease progression and quality of life
Kölker, S
Therapeutic modulation of cerebral lysine metabolism in a mouse model for glutaric aciduria type I
Kolodziejczyk, D
Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection
"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis
12 years of pediatric epilepsy surgery – The Vogtareuth experience
Korenke, GC
Congenital mirror movements in a family with a novel mutation in the DCC gene
Korinthenberg, R
Infantile epileptic encephalopathy due to cobalamin deficiency?
Resective surgery for refractory epilepsy in children under 4 years of age
Cognitve impairment as a leading symptom in juvenile MS – two case reports -
Kotzaeridou, U
PDH deficiency: identification of a novel mutation in the PDHA1gene in twins with intermittent weakness, resembling Guillain-Barré syndrome
Kovacevic-Preradovic, T
Isolated corpus callosum agenesis as a rare differenzial diagnosis of attention defficit hyperactivity disorder- case report
Koy, A
Crossed cerebellar diaschisis after status epilepticus
Krägeloh-Mann, I
Semi-Automatic quantification of demyelination load in children with metachromatic leukodystrophy on MR-images
Selective dorsal rhizotomy – selection criteria and outcome in the frst year after a new etablished invasive treatment
Comparison of different tractography algorithms and validation by intraoperative stimulation in a child with a brain tumor
Patients with neuromuscular scoliosis after spinal fusion and instrumentation: clinical, radiometric and functional results
Krajewska-Walasek, M
Identification of a second major locus for neurodegeneration with brain iron accumulation
Kraus, V
Treatment of severe childhood Multiple Sclerosis with plasmapheresis
Neurological presentations in children with serological active mycoplasma pneumoniae infection
Kress, W
A patient with mutations in the dystrophin and the FKRP gene – „double trouble“ or incidental finding
SelenoproteinN1-related myopathy: From clinical signs to diagnosis
Kretzschmar, H
Identification of a second major locus for neurodegeneration with brain iron accumulation
Kries, R von
CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort
Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results
Kroisl, P
Microdeletion 10q26-syndrome – A rare cause for developmental retardation, strabismus and hypoplasia of cerebellum – A case report
Kröpfl, T
Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: discussion of different phenotypes in two pediatric patients
Krumbholz, M
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Kudernatsch, M
Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions
Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection
Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome
Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients
Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion
"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis
Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy
12 years of pediatric epilepsy surgery – The Vogtareuth experience
Reoperations and second step-procedures in pediatric epilepsy surgery – indications, new techniques, limitations and results
Kujat, A
Emotional lability as a leading symptom of tetrasomy 18p in a 7-year-old girl with developmental delay, hypertonus of the adductors, kyphosis and facial anomalies
Kull-Sadacharam, K
Sensory – Integrative Ayres Therapie SIAT® – www.gsid.de
Kumar, V
Comparison of different tractography algorithms and validation by intraoperative stimulation in a child with a brain tumor
Kummer, S
How do we sedate children undergoing CSF opening pressure measurement? Results of a Germany-wide survey
Kümpfel, T
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Kurlemann, G
Differenzial diagnosis of acute encephalopathy: Acute decompensation in ornithine transcarbamylase (OTC) deficiency in a seven year old girl
Hereditary sensory and autonomic neuropathy Type IV – a case report with detection of two previously unknown sequence variants in NTKR1 gene
Potocki-Shaffer Syndrome: A case study
Kutsche, K
Congenital mirror movements in a family with a novel mutation in the DCC gene
Kutschke, G
A case of familial Labrune syndrome
Laage-Gaupp, A
Therapy of Hemiparesis in children and adolescents – a 5 years experience
Lämmer, C
Repeated bilateral dystonic elevation of visual gaze in a 15-year-old girl
Lanator, I
Early plasmapheresis in 3 consecutive cases of choreo-athetotic movement disorder after HSV-1 encephalitis
Lange-Hüsken, F
Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences
Langhagen, T
Disturbances of the vestibular and ocular motor systems in children with demyelinisating disorders of the central nervous system
Vitamin D levels in pediatric Multiple Sclerosis patients
Latal, B
Qualitative and quantitative motor performance in adolescents with CHD
Morphometric MRI findings in adolescents with congenital heart disease
Lauffer, H
Drug resistant seizures at the age of 3 months – mild form of a non-ketotic hyperglycinemia (NKH)
Stiff-persons syndrome in a 12 year old child – a case report
Leis, T
Development of pretems <1500g in the first two years of life: Standardized testing according to the Griffith Scales and Mental Bayley Scales
Leiz, S
Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine
Neuroborreliosis with cerebrovascular disease causes ischemic stroke in a 12 year old boy
Longitudinally very extensive acute transverse myelitis after influenza vaccination
Lengnick, K
Ongoing improvement in mobility, activity and cognition of a teenage girl with pediatric multiple sclerosis after 3 years of natalizumab treatment – a case report
Lidzba, K
Analysis of the control condition of a language fMRI task: a simple alternative to assess visuospatial functions?
Linder-Lucht, M
Inv dup (15) syndrome and refractory epilepsy: A case-report
AWMF-Guideline developmental coodination disorder: definition and assessment
AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention
Lippert, M
Therapy of Hemiparesis in children and adolescents – a 5 years experience
Logeswaran, T
Neurocognitive deficits in children requiring heart transplantation during infancy
Lotte, J
Urolithiasis with Topiramate and Zonisamide: Therapy? Prophylaxis?
Louwen, F
Fluid accumulation in the fetal extracerebral spaces: External hydrocephalus or subdural hygromas?
Lübbig, A
Urolithiasis with Topiramate and Zonisamide: Therapy? Prophylaxis?
Lücke, T
Neurodevelopmental outcome at 24 and 36 months of age in very low birth weight infants assessed by Bayley Scales of Infant Development II
Optical Coherence Tomography in neuro-pediatric diseases – A case report
Dissociative gait disturbance versus Guillain-Barré-Syndrom -pitfalls in clinical presentation and diagnostics
Lüdtke, U
Reversible hepatopathy during beta-interferone therapy of Multiple Sclerosis
Luef, G
Old and new antiepileptic drugs during pregnancy and lactation – report of a case
Lutz, S
Ataxia telangiectasia in dizygotic two year old twins
A patient with mutations in the dystrophin and the FKRP gene – „double trouble“ or incidental finding
SelenoproteinN1-related myopathy: From clinical signs to diagnosis
Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)
Glucocorticoid therapy in a non-ambulant six-year-old boy with Duchenne muscular dystrophy
Maak, A
Congenital mirror movements in a family with a novel mutation in the DCC gene
Madignier, F
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients
Magalhaes, S
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Mainberger, F
A four day course of Lovastatin improves synaptic plasticity in patients with NF-1
Makowski, C
Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation
Biochemical and genetic testing in a large cohort of patients with suspicion of mitochondriopathy
Multiple ischemic strokes in a case of Transient Cerebral Arteriopathy (TCA) following chickenpox
Treatment of severe childhood Multiple Sclerosis with plasmapheresis
Neurological presentations in children with serological active mycoplasma pneumoniae infection
Longitudinally very extensive acute transverse myelitis after influenza vaccination
Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum
Mall, V
A four day course of Lovastatin improves synaptic plasticity in patients with NF-1
CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort
Therapy of Hemiparesis in children and adolescents – a 5 years experience
Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results
Standardized and validated evaluation of groß motor function of children with cerebral palsy: Establishment of the Gross Motor Function Measure in German speaking countries
Cognitve impairment as a leading symptom in juvenile MS – two case reports -
Manero Borràs, RM
Inv dup (15) syndrome and refractory epilepsy: A case-report
Marquard, K
Tumefactive demyelinating lesion – a rare manifestation of multiple sclerosis in childhood
Marquardt, T
Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine
Marschall, C
Spine fracture following generalized tonic-clonic seizures in a 16 years old girl. An unusual case
Martinez, A
High incidence of paediatric CNS demyelination in East London
Mayatepek, E
How do we sedate children undergoing CSF opening pressure measurement? Results of a Germany-wide survey
Childhood arterial ischemic stroke related to anabolic steroid and cannabis abuse
Crossed cerebellar diaschisis after status epilepticus
Mayer, H
Neuropsychological and social functions in children and adoloescents with hypothalamic harmatomas
Mayer, T
Isolated corpus callosum agenesis as a rare differenzial diagnosis of attention defficit hyperactivity disorder- case report
Mayr, J
Deficiency of the mitochondrial phosphate carrier as a cause of combined mitochondrial (cardio-)myopathy
Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening
Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients
Mayr, JA
Pyruvate dehydrogenase deficiency presenting as Guillain-Barré syndrome
Meinl, E
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Meitinger, T
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients
Familiarity and course of specific language impairment of 175 children
Identification of a second major locus for neurodegeneration with brain iron accumulation
Mengel, E
The new Gaucher-Pass: A key tool in management of shortage
Meoded, A
Postnatal in-vivo MRI findings in anencephaly
Merkenschlager, A
Successful bevacizumab therapy for CNS radiation necrosis after stereotactic radiotherapy of an arteriovenous malformation
TENS therapy in tension headaches – little helps much?!
Emotional lability as a leading symptom of tetrasomy 18p in a 7-year-old girl with developmental delay, hypertonus of the adductors, kyphosis and facial anomalies
Myoclonus, ataxia and dancing eyes – visual diagnosis with diverse phenotype. Two cases of Opsoclonus-Myoclonus-Syndrome after adenoviral infection and scarlet fever
Pyruvate dehydrogenase deficiency presenting as Guillain-Barré syndrome
Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus
Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex
Mettin, RR
Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex
Meyer, H
Resective surgery for refractory epilepsy in children under 4 years of age
Meyer, S
Constraint-induced movement therapy versus bimanual therapy for children with central hemiparesis – relative effectiveness and factors of influence
Michaelis, U
Therapy of Hemiparesis in children and adolescents – a 5 years experience
Standardized and validated evaluation of groß motor function of children with cerebral palsy: Establishment of the Gross Motor Function Measure in German speaking countries
Mirjam, L
TENS therapy in tension headaches – little helps much?!
Mittelbronn, M
Fluid accumulation in the fetal extracerebral spaces: External hydrocephalus or subdural hygromas?
Moog, U
Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia
Cohen syndrome – an important differenzial diagnosis for children with mental retardation and secondary microcephaly
Mörzinger, M
Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study
Mueller-Felber, W
Identification of a second major locus for neurodegeneration with brain iron accumulation
Mühlebner, A
Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study
Müller, A
Urolithiasis with Topiramate and Zonisamide: Therapy? Prophylaxis?
First observations of treatment with rufinamide in children with myoclonic-astatic epilepsy
Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome
First experience of a parents questionnaire to define therapeutic goals for ketogenic diet in children with difficult-to-treat epilepsy
Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy
Müller-Felber, W
Disturbances of the vestibular and ocular motor systems in children with demyelinisating disorders of the central nervous system
Vitamin D levels in pediatric Multiple Sclerosis patients
Munteanu, M
Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)
Nagel, A
Robotic-assisted gait training improves gait parameters and functional mobility in patients wit cerebral palsy – preliminary results
Specific motion patterns of the sagittal, frontal and transversal plane in children with bilateral spastic cerebral palsy: Preliminary results of a cross-sectional study
Narayanan, U
CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort
Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results
Nauer, C
A vanishing cerebellar tumor – too good to be true
Navah, F
Resective surgery for refractory epilepsy in children under 4 years of age
Neidhardt, K
Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia
Neubauer, BA
PCDH19 defects in girls with infantile myoclonic epilepsy with and without autism
Neurocognitive deficits in children requiring heart transplantation during infancy
Postanoxic myoclonus (Lance-Adams syndrome) after near-drowning
Ney, S
Therapy of Hemiparesis in children and adolescents – a 5 years experience
Niemeyer, T
Patients with neuromuscular scoliosis after spinal fusion and instrumentation: clinical, radiometric and functional results
Nikanorova, M
Rufinamide. A new therapeutic option for epilepsy with myoclonic absences
Nögel, SC
Development of pretems <1500g in the first two years of life: Standardized testing according to the Griffith Scales and Mental Bayley Scales
Nolte-Buchholtz, S
Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy
Noss, J
Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine
Nüßlein, T
Reversible hepatopathy during beta-interferone therapy of Multiple Sclerosis
Oexle, K
Identification of a second major locus for neurodegeneration with brain iron accumulation
Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum
Oh, J
Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences
Okun, JG
Therapeutic modulation of cerebral lysine metabolism in a mouse model for glutaric aciduria type I
Olsson, I
Migraine – the chameleon of diseases
Olsson, T
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Olze, A
Efficacy and safety of oral lacosamide as adjunctive therapy in children under 16 years with partial-onset seizures
Opladen, T
Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia
Opp, S
Therapeutic modulation of cerebral lysine metabolism in a mouse model for glutaric aciduria type I
Pahs, G
Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study
Pannek, HW
Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009
Pascher, B
Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions
Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection
Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients
Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion
"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis
Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy
12 years of pediatric epilepsy surgery – The Vogtareuth experience
First experience of a parents questionnaire to define therapeutic goals for ketogenic diet in children with difficult-to-treat epilepsy
Penzien, J
Anti-NMDAR Encephalitis in children: Delineation of the epileptic phenotypes
Pereira, B
CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort
Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results
Peters, J
Neuroborreliosis with cerebrovascular disease causes ischemic stroke in a 12 year old boy
Pfister, ED
Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation
Pfurtscheller, K
Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: discussion of different phenotypes in two pediatric patients
Philippi, H
Canadian Occupational Performance Measure (COPM): A client- centered interview in parents and children with movement disorders
Pieper, T
Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions
Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection
Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome
Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients
Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion
"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis
Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy
12 years of pediatric epilepsy surgery – The Vogtareuth experience
Reoperations and second step-procedures in pediatric epilepsy surgery – indications, new techniques, limitations and results
Pietz, J
Modification of epileptiform activity by blocking glial glutamate uptake
PDH deficiency: identification of a novel mutation in the PDHA1gene in twins with intermittent weakness, resembling Guillain-Barré syndrome
Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia
Cohen syndrome – an important differenzial diagnosis for children with mental retardation and secondary microcephaly
Plecko, B
Status epilepticus in a newborn – pyridoxine toxicity?
Multiple arteriovenous malformations of the brain: A case report
Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: discussion of different phenotypes in two pediatric patients
Microdeletion 10q26-syndrome – A rare cause for developmental retardation, strabismus and hypoplasia of cerebellum – A case report
Pletziger, E
Encephalitis of varizella-zoster in a 26 months old child
Plümpe, N
Hereditary prosopagnosia
Pohl, D
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Pöhler, V
PCDH19 defects in girls with infantile myoclonic epilepsy with and without autism
Polatajko, H
AWMF-Guideline developmental coodination disorder: definition and assessment
AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention
Polster, T
Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009
Poretti, A
Postnatal in-vivo MRI findings in anencephaly
Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients
Poths, S
Canadian Occupational Performance Measure (COPM): A client- centered interview in parents and children with movement disorders
Preisler, B
The treatment of young children with low trunkal tone, as a result of various diagnoses, with dynamic GPS Soft Orthoses – case studies
Pröbstel, AK
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Prokisch, H
Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation
Biochemical and genetic testing in a large cohort of patients with suspicion of mitochondriopathy
Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients
Identification of a second major locus for neurodegeneration with brain iron accumulation
Prothmann, A
Multiple ischemic strokes in a case of Transient Cerebral Arteriopathy (TCA) following chickenpox
Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum
Pyper, A
Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy
Raabe, C
Therapy of Hemiparesis in children and adolescents – a 5 years experience
Selective dorsal rhizotomy – selection criteria and outcome in the frst year after a new etablished invasive treatment
Ramantani, G
Resective surgery for refractory epilepsy in children under 4 years of age
Rauchenzauner, M
Old and new antiepileptic drugs during pregnancy and lactation – report of a case
Rauscher, C
Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening
Reihle, C
Tumefactive demyelinating lesion – a rare manifestation of multiple sclerosis in childhood
Reinke, J
The new Gaucher-Pass: A key tool in management of shortage
Reiserer, B
Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy
Reiter-Fink, E
Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study
Reithofer, E
Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study
Reitter, A
Fluid accumulation in the fetal extracerebral spaces: External hydrocephalus or subdural hygromas?
Reitter, B
Isolated, monocular vertical nystagmus: single symptom of an extensive intracerebral tumor
A case of familial Labrune syndrome
Reutlinger, C
Successful treatment of parainfectious encephalitis with ivIG in a boy with FraX
Rhein, M von
The new Gaucher-Pass: A key tool in management of shortage
Qualitative and quantitative motor performance in adolescents with CHD
Morphometric MRI findings in adolescents with congenital heart disease
Isolated, monocular vertical nystagmus: single symptom of an extensive intracerebral tumor
Richterich, A
Psychopathology in CLN3 disease: Correlation with disease progression and quality of life
Dissociative gait disturbance versus Guillain-Barré-Syndrom -pitfalls in clinical presentation and diagnostics
Richwien, R
Multileveltherapy with botulinumtoxin A in children with cerebral movement disorders
Rienhardt, C von
Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy
Ries, M
Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia
Rivera-Brugués, N
Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum
Robl, H
Online EEG analysis by an epilepsy center
Rocamora Zúñiga, R
Inv dup (15) syndrome and refractory epilepsy: A case-report
Roeber, S
Identification of a second major locus for neurodegeneration with brain iron accumulation
Roland-Schäfer, D
Selective dorsal rhizotomy – selection criteria and outcome in the frst year after a new etablished invasive treatment
Rolinski, B
Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation
Biochemical and genetic testing in a large cohort of patients with suspicion of mitochondriopathy
Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients
Roloff-Messing, V
Complete occlusion of the left internal carotid artery in neurofibromatosis type 1. Congenital dysplasia or progressive occlusion?
Romein, E
Usefulness of RemiPro for pediatric neurorehabilitation in severe head injury: A case report
Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy
Roquer González, J
Inv dup (15) syndrome and refractory epilepsy: A case-report
Rosenbaum, T
Spine fracture following generalized tonic-clonic seizures in a 16 years old girl. An unusual case
Complete occlusion of the left internal carotid artery in neurofibromatosis type 1. Congenital dysplasia or progressive occlusion?
Hereditary prosopagnosia
Rosenberger, G
Congenital mirror movements in a family with a novel mutation in the DCC gene
Rostasy, K
Old and new antiepileptic drugs during pregnancy and lactation – report of a case
Unrecognized citrullinemia mimicking encephalitis in a 14 year-old boy – the role of a standardized lumbar puncture protocol
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Rostásy, K
Suspected bromide intoxication due to ketogenic diet?
Rötzer, K
Microdeletion 10q26-syndrome – A rare cause for developmental retardation, strabismus and hypoplasia of cerebellum – A case report
Rufino, A
Migraine – the chameleon of diseases
Rülander, C
Spine fracture following generalized tonic-clonic seizures in a 16 years old girl. An unusual case
Rutsch, F
Differenzial diagnosis of acute encephalopathy: Acute decompensation in ornithine transcarbamylase (OTC) deficiency in a seven year old girl
Sandrieser, T
Reversible hepatopathy during beta-interferone therapy of Multiple Sclerosis
Sauer, SW
Therapeutic modulation of cerebral lysine metabolism in a mouse model for glutaric aciduria type I
Saur, V
Neuroborreliosis with cerebrovascular disease causes ischemic stroke in a 12 year old boy
Schaaf, K
Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)
Schaefer, C
Qualitative and quantitative motor performance in adolescents with CHD
Schäfer, J
Therapy of Hemiparesis in children and adolescents – a 5 years experience
Schäfer, JS
Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?
Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy
Schallner, J
Reference intervals of plasma catecholamines in newborns for diagnosis of Menkes disease
Schara, U
Health- related quality of life in patients with Duchenne Muscular Dystrophy
Ataxia telangiectasia in dizygotic two year old twins
An unusual tremor
A patient with mutations in the dystrophin and the FKRP gene – „double trouble“ or incidental finding
SelenoproteinN1-related myopathy: From clinical signs to diagnosis
Growth and pubertal development of boys with x-chromosomal recessive Duchenne's muscular dystrophy (DMD)
Glucocorticoid therapy in a non-ambulant six-year-old boy with Duchenne muscular dystrophy
Schauer, U
Neurodevelopmental outcome at 24 and 36 months of age in very low birth weight infants assessed by Bayley Scales of Infant Development II
Scheer, I
Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients
Scheffner, T
Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation
Schiegl, H
Phacomatosis pigmentovascularis and extensive venous malformation of brain vessels. A unknown association or a new vascular neurocutaneous syndrome?
Schilling, M
The role of sharp wave activity in the consolidation of learning during sleep
Schimmel, M
Suspected bromide intoxication due to ketogenic diet?
Schmid, J
Health- related quality of life in patients with Duchenne Muscular Dystrophy
Schmidt, T
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Schmook, MT
Early plasmapheresis in 3 consecutive cases of choreo-athetotic movement disorder after HSV-1 encephalitis
Schneider, C
Activation of neuronal migration factor CXCR4 by pharmacological HIF stabilization in developing mouse brain
Schneider, HC
Deficiency of the mitochondrial phosphate carrier as a cause of combined mitochondrial (cardio-)myopathy
Schoemaker, M
AWMF-Guideline developmental coodination disorder: definition and assessment
AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention
Schoene-Bake, JC
A method for automated volumetry to assess disease progression in Rasmussen Encephalitis
Scholl-Buergi, S
Suspected bromide intoxication due to ketogenic diet?
Scholl-Bürgi, S
Unrecognized citrullinemia mimicking encephalitis in a 14 year-old boy – the role of a standardized lumbar puncture protocol
Schönfelder, J
A case of sudden cardiac death in a patient with LPIN1 gene mutation
Schröder, AS
Therapy of Hemiparesis in children and adolescents – a 5 years experience
Unicentric cohortstudy in children with bilateral spastic cerebral palsy about the drop out reasons after the first treatment with botulinumtoxin within a multi-modal therapy concept
The application of the German hip surveillance protocol in children with bilateral spastic cerebral palsy – a single centre cohort study
Schröder, C
Stiff-persons syndrome in a 12 year old child – a case report
Schröder, SA
Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?
Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy
Schroeder, AS
CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort
Schroeder, S
Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results
Schubert, C
Mitochondrial Neuronal Gastrointestinal Encephalopathy (MNGIE): Differenzial diagnosis of gastrointestinal motility disorder, leucencephalopathy, peripheral neuropathy without mental retardation
Schubert, S
Resective surgery for refractory epilepsy in children under 4 years of age
Schucht, P
A vanishing cerebellar tumor – too good to be true
Schugal, A
High incidence of paediatric CNS demyelination in East London
Schuhmann, M
Selective dorsal rhizotomy – selection criteria and outcome in the frst year after a new etablished invasive treatment
Schuhmann, MU
Comparison of different tractography algorithms and validation by intraoperative stimulation in a child with a brain tumor
Schulte-Markwort, M
Psychopathology in CLN3 disease: Correlation with disease progression and quality of life
Schulz, A
Psychopathology in CLN3 disease: Correlation with disease progression and quality of life
Schulze-Bonhage, A
Resective surgery for refractory epilepsy in children under 4 years of age
Schuster, V
Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus
Schwab, KO
Infantile epileptic encephalopathy due to cobalamin deficiency?
Schwahn, B
Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine
Schwerin-Nagel, A
Microdeletion 10q26-syndrome – A rare cause for developmental retardation, strabismus and hypoplasia of cerebellum – A case report
Schwindt, W
Potocki-Shaffer Syndrome: A case study
Seidl, R
Early plasmapheresis in 3 consecutive cases of choreo-athetotic movement disorder after HSV-1 encephalitis
Seidlitz, G
Drug resistant seizures at the age of 3 months – mild form of a non-ketotic hyperglycinemia (NKH)
Seitz, A
Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia
Siebers-Renelt, U
Potocki-Shaffer Syndrome: A case study
Siegel, C
Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum
Sigler, C
Late-onset folinic acid-responsive seizures
Smitka, M
Reference intervals of plasma catecholamines in newborns for diagnosis of Menkes disease
A case of sudden cardiac death in a patient with LPIN1 gene mutation
Integrating pediatric palliative care across the spectrum of life threatening pediatric neuromuscular disorders focused on Spinal muscular atrophy type I and Duchenne muscular dystrophy
Smits-Engelsman, B
AWMF-Guideline developmental coodination disorder: definition and assessment
AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention
Sömmer, J
Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy
Sorantin, E
Multiple arteriovenous malformations of the brain: A case report
Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis: discussion of different phenotypes in two pediatric patients
Sperl, P
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Sperl, W
Deficiency of the mitochondrial phosphate carrier as a cause of combined mitochondrial (cardio-)myopathy
Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening
Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients
Pyruvate dehydrogenase deficiency presenting as Guillain-Barré syndrome
Spescha, H
Ongoing improvement in mobility, activity and cognition of a teenage girl with pediatric multiple sclerosis after 3 years of natalizumab treatment – a case report
Spiegler, J
Successful treatment of parainfectious encephalitis with ivIG in a boy with FraX
Sprinz, A
Robotic-assisted gait training improves gait parameters and functional mobility in patients wit cerebral palsy – preliminary results
Specific motion patterns of the sagittal, frontal and transversal plane in children with bilateral spastic cerebral palsy: Preliminary results of a cross-sectional study
Glucocorticoid therapy in a non-ambulant six-year-old boy with Duchenne muscular dystrophy
Stark, W
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Staudt, M
Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions
Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection
Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome
Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients
Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion
"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis
Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy
12 years of pediatric epilepsy surgery – The Vogtareuth experience
Objective identification of successful performed clinical fMRI in children
Therapy of Hemiparesis in children and adolescents – a 5 years experience
Reoperations and second step-procedures in pediatric epilepsy surgery – indications, new techniques, limitations and results
Usefulness of RemiPro for pediatric neurorehabilitation in severe head injury: A case report
Stein, S
Standardized and validated evaluation of groß motor function of children with cerebral palsy: Establishment of the Gross Motor Function Measure in German speaking countries
Steiner, F
AWMF-Guideline developmental coodination disorder: definition and assessment
AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention
Steinlin, M
Acquired isolated focal cerebellar lesions during development: effect on cognition?
A vanishing cerebellar tumor – too good to be true
Stephani, U
Resective surgery for refractory epilepsy in children under 4 years of age
Sterl, E
Multiple arteriovenous malformations of the brain: A case report
Stevanowa, N
Familiarity and course of specific language impairment of 175 children
Storck, M
Cerebral palsy: Predictors of psychosocial development
Storm van's Gravesande, K
Cognitve impairment as a leading symptom in juvenile MS – two case reports -
Straube, A
A four day course of Lovastatin improves synaptic plasticity in patients with NF-1
Striano, P
Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome
Strobl, K
Neuropsychological and social functions in children and adoloescents with hypothalamic harmatomas
Resective surgery for refractory epilepsy in children under 4 years of age
Stroet, A
Optical Coherence Tomography in neuro-pediatric diseases – A case report
Strom, TM
Identification of a second major locus for neurodegeneration with brain iron accumulation
Strotmann, P
Treatment of severe childhood Multiple Sclerosis with plasmapheresis
Neurological presentations in children with serological active mycoplasma pneumoniae infection
Strupp, M
Disturbances of the vestibular and ocular motor systems in children with demyelinisating disorders of the central nervous system
Stülpnagel, C von
Urolithiasis with Topiramate and Zonisamide: Therapy? Prophylaxis?
First observations of treatment with rufinamide in children with myoclonic-astatic epilepsy
Low long-term efficacy of the orphan drug Rufinamide in patients with Dravet syndrome
First experience of a parents questionnaire to define therapeutic goals for ketogenic diet in children with difficult-to-treat epilepsy
Syrbe, S
Successful bevacizumab therapy for CNS radiation necrosis after stereotactic radiotherapy of an arteriovenous malformation
TENS therapy in tension headaches – little helps much?!
Emotional lability as a leading symptom of tetrasomy 18p in a 7-year-old girl with developmental delay, hypertonus of the adductors, kyphosis and facial anomalies
Myoclonus, ataxia and dancing eyes – visual diagnosis with diverse phenotype. Two cases of Opsoclonus-Myoclonus-Syndrome after adenoviral infection and scarlet fever
Pyruvate dehydrogenase deficiency presenting as Guillain-Barré syndrome
Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus
Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex
Tacke, UH
Infantile epileptic encephalopathy due to cobalamin deficiency?
Tantsis, E
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Tatagiba, M
Selective dorsal rhizotomy – selection criteria and outcome in the frst year after a new etablished invasive treatment
Tauer, U
Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation
Tegetmeyer, H
Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus
Teig, N
Neurodevelopmental outcome at 24 and 36 months of age in very low birth weight infants assessed by Bayley Scales of Infant Development II
Tesarova, M
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients
Thiele, S
Drug resistant seizures at the age of 3 months – mild form of a non-ketotic hyperglycinemia (NKH)
Stiff-persons syndrome in a 12 year old child – a case report
Thiels, C
Dissociative gait disturbance versus Guillain-Barré-Syndrom -pitfalls in clinical presentation and diagnostics
Thümmler, K
Constraint-induced movement therapy versus bimanual therapy for children with central hemiparesis – relative effectiveness and factors of influence
Tibussek, D
How do we sedate children undergoing CSF opening pressure measurement? Results of a Germany-wide survey
Toelle, SP
Phacomatosis pigmentovascularis and extensive venous malformation of brain vessels. A unknown association or a new vascular neurocutaneous syndrome?
Trantakis, C
Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus
Triltsch-Ciurea, I
Familiarity and course of specific language impairment of 175 children
Trimmel-Schwahofer, P
Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study
Trollmann, R
Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation
Activation of neuronal migration factor CXCR4 by pharmacological HIF stabilization in developing mouse brain
Development of pretems <1500g in the first two years of life: Standardized testing according to the Griffith Scales and Mental Bayley Scales
Isolated optic neuritis is associated with development of pediatric multiple sclerosis
Tuxhorn, I
Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009
Utz, N
Complete occlusion of the left internal carotid artery in neurofibromatosis type 1. Congenital dysplasia or progressive occlusion?
Utzig, N
Stiff-persons syndrome in a 12 year old child – a case report
Uziel, G
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Valls Santasusana, A
Inv dup (15) syndrome and refractory epilepsy: A case-report
Valsangiacomo, ER
Qualitative and quantitative motor performance in adolescents with CHD
van Velthofen, V
Resective surgery for refractory epilepsy in children under 4 years of age
Villalobos, A
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Vivanco Hidalgo, RM
Inv dup (15) syndrome and refractory epilepsy: A case-report
Wagner, J
A method for automated volumetry to assess disease progression in Rasmussen Encephalitis
Wagner, K
Microdeletion 10q26-syndrome – A rare cause for developmental retardation, strabismus and hypoplasia of cerebellum – A case report
Wagner, M
Congenital mirror movements in a family with a novel mutation in the DCC gene
Wagner, O
Severe neonatal myopathy due to SUCLG1 deficiency with methylmalonic aciduria detected via newborn screening
Wahlländer-Danek, U
A four day course of Lovastatin improves synaptic plasticity in patients with NF-1
Waibel, P
Ongoing improvement in mobility, activity and cognition of a teenage girl with pediatric multiple sclerosis after 3 years of natalizumab treatment – a case report
Walkinshaw, G
Activation of neuronal migration factor CXCR4 by pharmacological HIF stabilization in developing mouse brain
Walsh, S
Kleine-Levin syndrome: a disorder with recurring hypersomnia as main symptom
Familial occurence of congenital bilateral perisylvian syndrom
Warken, B
Does a second robotic assisted intensified treadmill training (Lokomat®) add to the functional improvement in children with bilateral spastic cerebral palsy?
Is the Gross Motor Function Measure (GMFM 66) a sensitive tool to represent the therapeutic improvement after robotic assisted treadmill training? A controlled study about the therapeutic effect of Lokomat® therapy
Weber, AA
Childhood arterial ischemic stroke related to anabolic steroid and cannabis abuse
Crossed cerebellar diaschisis after status epilepticus
Weber, B
A method for automated volumetry to assess disease progression in Rasmussen Encephalitis
Weber, F
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Weber-Sannwald, A
Canadian Occupational Performance Measure (COPM): A client- centered interview in parents and children with movement disorders
Weibel, L
Phacomatosis pigmentovascularis and extensive venous malformation of brain vessels. A unknown association or a new vascular neurocutaneous syndrome?
Weigt-Usinger, K
Neurodevelopmental outcome at 24 and 36 months of age in very low birth weight infants assessed by Bayley Scales of Infant Development II
Optical Coherence Tomography in neuro-pediatric diseases – A case report
Dissociative gait disturbance versus Guillain-Barré-Syndrom -pitfalls in clinical presentation and diagnostics
Weimer, W
Differenzial diagnosis of acute encephalopathy: Acute decompensation in ornithine transcarbamylase (OTC) deficiency in a seven year old girl
Hereditary sensory and autonomic neuropathy Type IV – a case report with detection of two previously unknown sequence variants in NTKR1 gene
Weir, S
CPchild – caregiver priorities and child health index of live with disabilities – initial validation in a german cohort
Influence of hip luxation on health related quality of life (HRQL) in children with cerebral palsy evaluated by the CP-CHILD questionaire – preliminary results
Weiss, D
Kleine-Levin syndrome: a disorder with recurring hypersomnia as main symptom
Familial occurence of congenital bilateral perisylvian syndrom
Weiss, K
Dog-assisted therapy for severe impaired children during inpatient early rehabilitation: Goals, content and efficacy
Weissert, M
Ongoing improvement in mobility, activity and cognition of a teenage girl with pediatric multiple sclerosis after 3 years of natalizumab treatment – a case report
Weissert, R
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Weitkämper, A
Neurodevelopmental outcome at 24 and 36 months of age in very low birth weight infants assessed by Bayley Scales of Infant Development II
Wekerle, H
Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis
Wenner, K
Neuromyelitis Optica versus Multiple Sclerosis- diagnostic and therapeutic differences
Wiegand, G
Resective surgery for refractory epilepsy in children under 4 years of age
Wiemer-Kruel, A
Modified Atkins diet as a treatment of epilepsy in 23 children
Wilke, M
Semi-Automatic quantification of demyelination load in children with metachromatic leukodystrophy on MR-images
Objective identification of successful performed clinical fMRI in children
Analysis of the control condition of a language fMRI task: a simple alternative to assess visuospatial functions?
Comparison of different tractography algorithms and validation by intraoperative stimulation in a child with a brain tumor
Wilken, B
Late-onset folinic acid-responsive seizures
Multileveltherapy with botulinumtoxin A in children with cerebral movement disorders
Wilson, P
AWMF-Guideline developmental coodination disorder: definition and assessment
AWMF clinical practice guideline Developmental Coordination Disorder: treatment indication and intervention
Wingeier, K
Acquired isolated focal cerebellar lesions during development: effect on cognition?
Winkelmann, J
Identification of a second major locus for neurodegeneration with brain iron accumulation
Winkler, PA
Invasive pre-surgical epilepsy diagnostic in children: The advantage of depth electrodes combined with subdural grids in the evaluation of focal cortical dysplastic lesions
Pediatric epilepsy surgery in patients with bilateral or extended brain lesions results of 22 patients with a primary incomplete resection
Focal epilepsy in children due to unilateral polymicrogyria: Decision making, surgical treatment and outcome
Pediatric epilepsy surgery in patients with phacomatosis: Postoperative outcome in 13 patients
Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion
"Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis
Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy
12 years of pediatric epilepsy surgery – The Vogtareuth experience
Reoperations and second step-procedures in pediatric epilepsy surgery – indications, new techniques, limitations and results
Winkler, T
A four day course of Lovastatin improves synaptic plasticity in patients with NF-1
Winkler, U
A case of sudden cardiac death in a patient with LPIN1 gene mutation
Wintergerst, U
Online EEG analysis by an epilepsy center
Wittig, I
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Woermann, F
Epilepsy surgery: Reoperations in children in the Epilepsy Centre Bethel from 1990 to 2009
Wolf, NI
Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia
Clinical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia
Wülker, N
Patients with neuromuscular scoliosis after spinal fusion and instrumentation: clinical, radiometric and functional results
Wüller, D
Encephalitis of varizella-zoster in a 26 months old child
Wüller, DH
The effect of Lamotrigin and Levetiracetam on the perinatal period
Wurm, RE
Successful bevacizumab therapy for CNS radiation necrosis after stereotactic radiotherapy of an arteriovenous malformation
Zarits, P
Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study
Zeder, SL
Multiple arteriovenous malformations of the brain: A case report
Zenker, M
A four day course of Lovastatin improves synaptic plasticity in patients with NF-1
Zentner, J
Resective surgery for refractory epilepsy in children under 4 years of age
Zeviani, M
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients
Zimmermann, F
Deficiency of the mitochondrial phosphate carrier as a cause of combined mitochondrial (cardio-)myopathy
Zsoter, A
Objective identification of successful performed clinical fMRI in children