Abstracts of the 35th Annual Meeting of the Society of Neuropediatrics

Abels, C.

Epilepsy in vitamin B12 deficiency and its treatment in infancy

Autosomal dominant chin myoclonus

Abicht, A.

mitoNET – German Network for mitochondrial disorders

Acham-Roschitz, B.

Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations

Achatz, E.

Homocystein as an important diagnostic marker of remethylation defects – A case report

Aebi, C.

Bannwarth's syndrome – A rare but important manifestation of neuroborreliosis in childhood

Ahtig, U.

Diagnostic strategy in mitochondrial disorders – An update

Ahting, U.

Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue

Aksu, F.

Quantitative Sensory Testing (QST) in children and adolescents

Alber, M.

Neurocysticercosis in a 10 year-old boy in Germany

Polyneuropathy and hepatopathy as an infantile manifestation of a POLG1 gene defect

Albrecht, U.

Cardiac arrest in a patient with glutaric aciduria type II

Alesch, F.

Deep-brain stimulation in a boy with DYT1 dystonia

Allkemper, T.

Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?

Arend, M.

Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)

Arning, L.

Ataxia with oculomotor apraxia 1 (AOA1) in a consanguineous Pakistanian familiy

Atypical clinical presentation of a girl with episodic ataxia type II

Ausserer, B.

Posterior reversible encephalopathy syndrome (PRES)

Bajer-Kornek, B.

Epidemiology of pediatric multiple sclerosis in Austria

Baldeweg, T.

Language lateralisation in childhood-onset focal epilepsy: Evidence from fMRI

Balmer, C.

Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development

Bast, T.

Hashimoto's encephalopathy with stroke-like episodes and optic neuritis in a 19-year-old patient

Baudhuin, J. A.

Rufinamide treatment in 18 patients with Lennox-Gastaut syndrome – Documentation with the electronic patient diary epivista®

Baumann, M.

Uncommon manifestations of childhood neuroborreliosis

Baumgartner, M.

Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development

Baumhackl, U.

Epidemiology of pediatric multiple sclerosis in Austria

Becher, T.

Sandifers syndrome – Unusual case report and review of the literature

Dystonic movements and developmental coordination disorder – Successful treatment with methylphenidate

Beck, M.

GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase

Becker, M.

Modified memory processes in children with febrile seizures: Analysis of event-related potentials

Beckhaus, M.

A series of 34 patients with Rasmussen's encephalitis: Clinical course, EEG- and MRI findings

Benninger, F.

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Ben-Omran, T.

GLUT1 deficiency syndrome in a consanguineous Arab family carrying a novel homozygous missense mutation

Bernhard, M. K.

Seizures caused by accidental dimenhydriante intoxication

Toxic effects of lamotrigine ingestion in children

Miller Fisher syndrome and Guillain Barré syndrome with ophtamloplegia: Two cases with overlapping phenotype

Therapy of headaches in children and adolescents with TENS (Transcutaneous Electrical Nerve Stimulation) – An observational study of the Children's Hospital of the University of Leipzig

Chronic fatigue and pain syndrome caused by persistent intoxication with cactus spurge in a 12-year-old girl

Bertsche, A.

Hashimoto's encephalopathy with stroke-like episodes and optic neuritis in a 19-year-old patient

GLUT1 deficiency in a child with a movement disorder

Berweck, S.

Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases

Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up

Safety of botulinum toxin treatment in children with cerebral palsy in correlation to GMFCS level

Correlation of botulinum toxin dosage and GMFCS level in children with bilateral spastic cerebral palsy – An explorative cohortstudy

Robotic-assisted treadmill therapy enhances motor functions in children with bilateral spastic cerebral palsy

Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia

Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia

Bevot, A.

Polyneuropathy and hepatopathy as an infantile manifestation of a POLG1 gene defect

Bien, C. G.

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder

Bigi, S.

Bannwarth's syndrome – A rare but important manifestation of neuroborreliosis in childhood

Therapy of sinus venous thrombosis in childhood – A standardised treatment protocol – Call for participation

Birnbacher, R.

Uncommon manifestations of childhood neuroborreliosis

Biste, M.

Improved molecular diagnostics for patients with respiratory chain complex deficiency

Bittner, R.

Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations

Blankenburg, M.

Quantitative Sensory Testing (QST) in children and adolescents

Blaschek, A.

Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)

Boekens, H.

Quantitative Sensory Testing (QST) in children and adolescents

Böhmer, S.

Copper histidine therapy started in a boy at the age of three years – Treatment option for a mild form of Menkes's disease

Boltshauser, E.

Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development

Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia

Pontine tegmental cap dysplasia: Two additional cases

Boor, R.

Rufinamide treatment in 18 patients with Lennox-Gastaut syndrome – Documentation with the electronic patient diary epivista®

Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes

Boppel, T.

Deep brain stimulation in children and adolescents with dystonia

Borggraefe, I.

Safety of botulinum toxin treatment in children with cerebral palsy in correlation to GMFCS level

Correlation of botulinum toxin dosage and GMFCS level in children with bilateral spastic cerebral palsy – An explorative cohortstudy

Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia

Borggräfe, I.

Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases

Robotic-assisted treadmill therapy enhances motor functions in children with bilateral spastic cerebral palsy

Bötzel, K.

Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia

Braulke, T.

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

Breuer, K.

Monosomy 9pter-p22 in a boy with neonatal hypoglycemia, epilepsy, facial dysmorphism and hypotonia

Brocke, K. S.

Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report

Brockmann, K.

Ophthalmoplegic migraine (OM) with early-onset recurrent oculomotor palsy of the left eye in a 6-year-old boy

Brück, W.

Natalizumab in 4 cases of pediatric multiple sclerosis

Brunner-Krainz, M.

20 years evaluation of pediatric patients with encephalitis in the PICU

Febrile seizures – First symptom of Rasmussenencephalitis

Homocystein as an important diagnostic marker of remethylation defects – A case report

Burdach, S.

Hennekam-syndrome with unusual MRI-changes and symptomatic epilepsy

Burfeind, P.

CDKL5 mutation in neonatal onset of epilepsy

Calaminus, G.

Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment

Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents

Christen, H. J.

Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation

Cowley, M. A.

Peripheral alpha MSH in childhood obesity and craniopharyngioma

Cross, J. H.

Language lateralisation in childhood-onset focal epilepsy: Evidence from fMRI

Czech, T.

Surgery during early life in children with intractable epilepsy – A prospective evaluation

Danek, A.

Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia

Das, A.

Treatment of NPC with miglustat in Germany

Manifestation and diagnosis of NPC disease in Germany

Das, A. M.

Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure

M. Scheie: Failure of enzyme replacement therapy to prevent CNS- and spinal-lesions

Datta, A. N.

Acute disseminated encephalomyelitis review in 8 pediatric patients

Daumer-Haas, C.

Accessory nipple as key symptom in diagnosis of Mowat-Wilson syndrome

Monosomy 9pter-p22 in a boy with neonatal hypoglycemia, epilepsy, facial dysmorphism and hypotonia

Davids, S.

Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity

Degos, V.

Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease

De Haan, B.

Early determination of somatosensory cortex

Della Marina, A.

Ataxia with oculomotor apraxia 1 (AOA1) in a consanguineous Pakistanian familiy

Delvendahl, I.

Does navigated transcranial magnetic stimulation (TMS) decrease the variability of motor evoked potentials (MEP) and increase its reproducibility?

Denecke, J.

A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity

Dercks, M.

Focal dystonia of dominant hand in a 13 year old girl: Action dystonia successfully treated by botulinumtoxine A (Xeomin®)

Treatment of cerebral palsy: Use of botulinum neurotoxin type A free of complexing proteins (Xeomin®) in childhood

Deuschle, K.

CDKL5 mutation in neonatal onset of epilepsy

Dickhaus, H.

Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)

Domin, M.

Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity

Donnerstag, F.

M. Scheie: Failure of enzyme replacement therapy to prevent CNS- and spinal-lesions

Drack, F.

Outcome of acute peripheral facial palsy in children – A catamnestic study of 84 patients

Drechsel-Baeuerle, U.

VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data

Dreiwes, C.

Rufinamide treatment in 18 patients with Lennox-Gastaut syndrome – Documentation with the electronic patient diary epivista®

Dressler, A.

Surgery during early life in children with intractable epilepsy – A prospective evaluation

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Drosten, C.

Neonatal encephalitis through human parechoviruses with signs of extensive white matter injury – Case study and comparison to existing published cases

du Plessis, A. J.

Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia

Dütting, T.

Neonatal encephalitis through human parechoviruses with signs of extensive white matter injury – Case study and comparison to existing published cases

Ebinger, F.

Hashimoto's encephalopathy with stroke-like episodes and optic neuritis in a 19-year-old patient

Acute motor and sensory axonal neuropathy (AMSAN) in a 7-year-old boy. A cases report

Deep brain stimulation in children and adolescents with dystonia

Treatment of NPC with miglustat in Germany

GLUT1 deficiency in a child with a movement disorder

Atypical clinical presentation of a girl with episodic ataxia type II

Manifestation and diagnosis of NPC disease in Germany

Eder, H. G.

Febrile seizures – First symptom of Rasmussenencephalitis

Ehrich, J. H. H.

Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure

Eichholz, S.

Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)

Einspieler, C.

Assessment of spontaneous movements in an infant with Peters anomaly

Is there an association between Touwen's neurological examination and the Zuerich neuromotor assessment?

Associated movements in 5- to 10-year-old infants

A possible association between genotypes and early signs of Rett disorder

The Preserved Speech Variant of Rett syndrome: Specificity of atypicality?

Elpers, C.

Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?

Emser, A.

Low grade glioma in pediatric NF-1 patients

Enrion, P. J.

Peripheral alpha MSH in childhood obesity and craniopharyngioma

Ertl-Wagner, B.

Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia

Erwa, W.

Homocystein as an important diagnostic marker of remethylation defects – A case report

Esser, N.

CDKL5 mutation in neonatal onset of epilepsy

Fahrig, A.

Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report

Faldum, A.

Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment

Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients

Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up

Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents

Fantur, K.

Imino analogues of galactose: Inhibitors of human acid β-D-Galactosidase and putative pharmacological chaperones for the treatment of GM1-Gangliosidosis

GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase

Feichtinger, M.

Febrile seizures – First symptom of Rasmussenencephalitis

Feucht, M.

Surgery during early life in children with intractable epilepsy – A prospective evaluation

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Do children with drug resistant epilepsy and low IQ also improve after epilepsy Ssrgery?

Fiedler, B.

Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?

Autosomal dominant chin myoclonus

A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity

Fiedler, B. J.

Epilepsy in vitamin B12 deficiency and its treatment in infancy

Fleischhack, G.

Severe generalized neuropathy in an 18-year-old patient with hereditary sensory-motor polyneurpathy (HMSN) type 1 treated with vincristine due to acute leukemia

Forstner, R.

Pontine tegmental cap dysplasia: Two additional cases

Fowler, B.

Homocystein as an important diagnostic marker of remethylation defects – A case report

Franke, A.

Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes

Freidl, T.

Opsoklonus-Myoklonus-Syndrom

Freilinger, M.

Surgery during early life in children with intractable epilepsy – A prospective evaluation

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Deep-brain stimulation in a boy with DYT1 dystonia

Freisinger, P.

Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue

Diagnostic strategy in mitochondrial disorders – An update

mitoNET – German Network for mitochondrial disorders

Improved molecular diagnostics for patients with respiratory chain complex deficiency

Frey, S. G.

Acute disseminated encephalomyelitis review in 8 pediatric patients

Fritsch, M. J.

Outcome of endoscopic therapy of complex hydrocephalus

Fuchs, T.

Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia

Ganslandt, O.

Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report

Gärtner, J.

Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency

Ophthalmoplegic migraine (OM) with early-onset recurrent oculomotor palsy of the left eye in a 6-year-old boy

The structure of tripeptidyl peptidase I (TPP1) provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis

Cerebral MRI as a valuable tool for the diagnosis of Zellweger syndrome spectrum patients and patients with peroxisomal β-oxidation defects

Natalizumab in 4 cases of pediatric multiple sclerosis

Cyclic Esotropia – A rare differenzial diagnosis in non paralytic strabismus in childhood

Gebhardt, U.

Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment

Peripheral alpha MSH in childhood obesity and craniopharyngioma

Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients

Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up

Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents

Gehrmann, A.

Intracerebral calcification in a newborn – Not always a connatal infection

Geis, T.

Tumor induced Hemichorea

Gerecke, A.

Wernicke encephalopathy in childhood

Gerstner, K.

Modified memory processes in children with febrile seizures: Analysis of event-related potentials

Gnekow, A.

Low grade glioma in pediatric NF-1 patients

Gontard, A. von

Modified memory processes in children with febrile seizures: Analysis of event-related potentials

Gortner, L.

Modified memory processes in children with febrile seizures: Analysis of event-related potentials

The prognostic value of EEG in children with minor head trauma

Gotwald, T.

Cardiac arrest in a patient with glutaric aciduria type II

Gouadon, E.

Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease

Gratzki, N.

Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report

Greiner, J.

Acute basilar artery thrombosis in childhood: A therapeutic dilemma

Grenzebach, U.

Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?

Gressens, P.

Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease

Grodd, W.

Diagnostic value of magnetic resonance imaging and morphometry of the corpus callosum in children with isolated mental retardation

A new score for assessing white matter changes in metachromatic leukodystrophy

Gronborg, S.

Cerebral MRI as a valuable tool for the diagnosis of Zellweger syndrome spectrum patients and patients with peroxisomal β-oxidation defects

Gröppel, G.

Surgery during early life in children with intractable epilepsy – A prospective evaluation

Gross, C. D.

Mutation analysis of the SCN1A gene for suspected Dravet syndrome/GEFS+ – High detection yield, unsatisfactory prognostic value

Gruber-Sedlmayr, U.

20 years evaluation of pediatric patients with encephalitis in the PICU

Plasmapheresis in the treatment of pediatric patients with neurological diseases: 10 years experience

Opsoklonus-Myoklonus-Syndrom

Grüne, T.

The structure of tripeptidyl peptidase I (TPP1) provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis

Grønborg, S.

Ophthalmoplegic migraine (OM) with early-onset recurrent oculomotor palsy of the left eye in a 6-year-old boy

Gudegast, C.

Outcome of endoscopic therapy of complex hydrocephalus

Haase, C.

Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease

Haas-Lude, K.

Neurocysticercosis in a 10 year-old boy in Germany

Haberlandt, E.

Proinflamatory cytokines in children with febrile seizures

Cardiac arrest in a patient with glutaric aciduria type II

Habermehl, P.

Case report: Rapid evolving, severe encephalopathy, caused by nutritive cobalamin deficiency due to subclinical maternal pernicious anemia

Long-term antikoagulation in a neonate with sinovenous thrombosis and stroke. Case presentation and review of the literature

Hackmann, K.

Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report

Hackstein, H.

IAHSP caused by maternal uniparental isodisomy in ALS2

Hadders-Algra, M.

Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)

Hagen, M. von der

Postinfectious autoimmune-mediated encephalitis versus relapse of herpes encephalitis?

Muscular magnet resonance imaging (M-MRI) in α-Dystroglykanopathies – clinical course of two juvenile patients with LGMD2I and LGMD2M

A rare Ca2+ channel mutation R528G identified in a patient with autosomal dominant hypokalemic periodic paralysis (HypoPP-1)

Hahn, A.

Non-invasive tension-time-index and ventilator use in Duchenne muscular dystrophy

Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease

Hahn, G.

Postinfectious autoimmune-mediated encephalitis versus relapse of herpes encephalitis?

Pontine tegmental cap dysplasia: Two additional cases

Muscular magnet resonance imaging (M-MRI) in α-Dystroglykanopathies – clinical course of two juvenile patients with LGMD2I and LGMD2M

Hahn, J.

Continous intrathecal baclofen (cITB) therapy terminates spinal spasms mimicking tonic seizures in a teenager with severe spastic cerebral palsy with total body involvement and cervical dystonia

Hainfellner, J.

Surgery during early life in children with intractable epilepsy – A prospective evaluation

Hamm, A.

Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity

Hampel, O.

Evaluation of Stepping Stones Triple P – 3-year-interims-analysis of the Stepping-Stones-SPC-Multicenter-Study

Hanganu, I.

KCNQ potassium channels are critical determinants of neuronal network activity in neonatal mouse brain

Hartig, M. B.

Clinical characterisation of NBIA patients with and without mutation in PANK2 gene

Hartmann, H.

Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure

M. Scheie: Failure of enzyme replacement therapy to prevent CNS- and spinal-lesions

Hartmann, M.

Oxcarbazepine accelerates steroid elimination in young men with epilepsy due to cytochrome P450 3A4 induction

Hartung, R.

Treatment of NPC with miglustat in Germany

Manifestation and diagnosis of NPC disease in Germany

Harzer, K.

Manifestation and diagnosis of NPC disease in Germany

Hasmann, R.

Evaluation of Stepping Stones Triple P – 3-year-interims-analysis of the Stepping-Stones-SPC-Multicenter-Study

Hasmann, S.

Evaluation of Stepping Stones Triple P – 3-year-interims-analysis of the Stepping-Stones-SPC-Multicenter-Study

Haug, V.

Severe confusion and agitation as predominant symptom of a hemiplegic migraine with mutation in ATP1A2

Hauschke, D.

Does navigated transcranial magnetic stimulation (TMS) decrease the variability of motor evoked potentials (MEP) and increase its reproducibility?

Hauser, E.

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Hawellek, N.

Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure

Hechler, T.

Quantitative Sensory Testing (QST) in children and adolescents

Hecker, A.

Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease

Heinen, F.

Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases

Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up

Safety of botulinum toxin treatment in children with cerebral palsy in correlation to GMFCS level

Correlation of botulinum toxin dosage and GMFCS level in children with bilateral spastic cerebral palsy – An explorative cohortstudy

Robotic-assisted treadmill therapy enhances motor functions in children with bilateral spastic cerebral palsy

Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia

Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia

Helbig, I.

Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes

VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data

Hempel, M.

Hennekam-syndrome with unusual MRI-changes and symptomatic epilepsy

Clinical characterisation of NBIA patients with and without mutation in PANK2 gene

Herbertz, S.

Fast recovery after 5 months in persistent vegetative state

Hernáiz Driever, P.

Low grade glioma in pediatric NF-1 patients

Herzfeld, T.

IAHSP caused by maternal uniparental isodisomy in ALS2

Himpel, M.

Therapy of headaches in children and adolescents with TENS (Transcutaneous Electrical Nerve Stimulation) – An observational study of the Children's Hospital of the University of Leipzig

Hirschburger, M.

Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease

Hirschfeld, H.

Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity

Hofer, D.

Imino analogues of galactose: Inhibitors of human acid β-D-Galactosidase and putative pharmacological chaperones for the treatment of GM1-Gangliosidosis

GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase

Hoffmann, G. F.

Multiple epiphyseal dysplasia as differenzial diagnosis in patients with L-Dopa responsive dystonia

Hoffmann, L.

Combination of early endotracheal Surfactant and nasal continous positive airwaypressure (CPAP): 15–32-month outcome of extremly low birth weight preterm infants (ELBW)

Högler, W.

Oxcarbazepine accelerates steroid elimination in young men with epilepsy due to cytochrome P450 3A4 induction

Holl, R.

Evaluation of Stepping Stones Triple P – 3-year-interims-analysis of the Stepping-Stones-SPC-Multicenter-Study

Holthausen, H.

Hemiplegic migraine with cerebellar atrophy: A second pediatric case

Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)

Hornstein, S.

Low grade glioma in pediatric NF-1 patients

Horvarth, R.

Improved molecular diagnostics for patients with respiratory chain complex deficiency

Horvath, R.

Polyneuropathy and hepatopathy as an infantile manifestation of a POLG1 gene defect

Hoy, L.

Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure

Huisman, T. A.

Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia

Huppke, B.

Natalizumab in 4 cases of pediatric multiple sclerosis

Huppke, P.

Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency

Ophthalmoplegic migraine (OM) with early-onset recurrent oculomotor palsy of the left eye in a 6-year-old boy

Natalizumab in 4 cases of pediatric multiple sclerosis

Huß, K.

Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases

Safety of botulinum toxin treatment in children with cerebral palsy in correlation to GMFCS level

Correlation of botulinum toxin dosage and GMFCS level in children with bilateral spastic cerebral palsy – An explorative cohortstudy

Ihorst, G.

Treatment of Duchenne muscular dystrophy with cyclosporin A – A randomized, double-blind, placebo controlled trial

Ikonomidou, C.

Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission

Muscular magnet resonance imaging (M-MRI) in α-Dystroglykanopathies – clinical course of two juvenile patients with LGMD2I and LGMD2M

Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report

Ikonomidou, H.

Postinfectious autoimmune-mediated encephalitis versus relapse of herpes encephalitis?

Illerhaus, M.

Focal dystonia of dominant hand in a 13 year old girl: Action dystonia successfully treated by botulinumtoxine A (Xeomin®)

Illsinger, S.

Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure

M. Scheie: Failure of enzyme replacement therapy to prevent CNS- and spinal-lesions

Isbrandt, D.

KCNQ potassium channels are critical determinants of neuronal network activity in neonatal mouse brain

Jagdhuhn, M.

Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity

Jäger, G.

Citrobacter koseri meningitis – A rare and severe disease in the neonate. A case report

Johann to Settel, E.

Severe generalized neuropathy in an 18-year-old patient with hereditary sensory-motor polyneurpathy (HMSN) type 1 treated with vincristine due to acute leukemia

Jopp-Petzinna, G.

Combination of early endotracheal Surfactant and nasal continous positive airwaypressure (CPAP): 15–32-month outcome of extremly low birth weight preterm infants (ELBW)

Juenemann, S.

Acute basilar artery thrombosis in childhood: A therapeutic dilemma

Juenger, H.

Early determination of somatosensory cortex

Jung, N. H.

Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up

Does navigated transcranial magnetic stimulation (TMS) decrease the variability of motor evoked potentials (MEP) and increase its reproducibility?

Jurkat-Rott, K.

A rare Ca2+ channel mutation R528G identified in a patient with autosomal dominant hypokalemic periodic paralysis (HypoPP-1)

Kabus, M.

Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)

Kaindl, A. M.

Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission

Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease

Neuropathologic findings in patients with primary autosomal recessive microcephaly

Karall, D.

Proinflamatory cytokines in children with febrile seizures

Cardiac arrest in a patient with glutaric aciduria type II

Karch, D.

Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)

Karnath, H. O.

Early determination of somatosensory cortex

Kasahara, M.

GLUT1 deficiency syndrome – A novel phenotype and a novel mutation

Kattner, E.

Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation

Kehrer, C.

Clinical course of two siblings with Metachromatic Leukodystrophy (MLD) with and without Stem cell transplantation (SCT)

A new score for assessing white matter changes in metachromatic leukodystrophy

Kehrer, M.

The development of cerebral perfusion during the first three years of life: Long-term follow-up study of cerebral blood flow volume measurement in two healthy children

Keller-Stanislawski, B.

VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data

Kerr, A. M.

A possible association between genotypes and early signs of Rett disorder

Keyvani, K.

A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity

Kiening, K.

Deep brain stimulation in children and adolescents with dystonia

Kim, K. S.

Full clinical recovery after acute haemolytic uraemic syndrome (HUS) with basal ganglia involvement and severe dystonia. A case report

Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)

Kim, S.

Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation

Kipp, K. H.

Modified memory processes in children with febrile seizures: Analysis of event-related potentials

Kirmess, B.

Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia

Kirschner, J.

Treatment of Duchenne muscular dystrophy with cyclosporin A – A randomized, double-blind, placebo controlled trial

Severe confusion and agitation as predominant symptom of a hemiplegic migraine with mutation in ATP1A2

Klaiber, M.

Robotic-assisted treadmill therapy enhances motor functions in children with bilateral spastic cerebral palsy

Klein, A.

Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development

Klepper, J.

Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency

GLUT1 deficiency syndrome – A novel phenotype and a novel mutation

GLUT1 deficiency syndrome in a consanguineous Arab family carrying a novel homozygous missense mutation

Klopstock, T.

mitoNET – German Network for mitochondrial disorders

Klose, J.

Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission

Kloss, M.

Deep brain stimulation in children and adolescents with dystonia

Kluger, G.

Provocation of seizures by vaccination with children suffering from SCN1A-mutation

Fast recovery after 5 months in persistent vegetative state

Patients with Dravet's syndrome and SCN1A-mutation with a benign course of illness – A case report with 6 patients

Kmiec, T.

Clinical characterisation of NBIA patients with and without mutation in PANK2 gene

Knecht, B.

Acute basilar artery thrombosis in childhood: A therapeutic dilemma

Knuf, M.

Case report: Rapid evolving, severe encephalopathy, caused by nutritive cobalamin deficiency due to subclinical maternal pernicious anemia

Long-term antikoagulation in a neonate with sinovenous thrombosis and stroke. Case presentation and review of the literature

Koch, J.

Uncommon manifestations of childhood neuroborreliosis

Treatment of West syndrome (WS) according to UKISS (United Kindom Infantile Spasms Study): A single centers experience

Pontine tegmental cap dysplasia: Two additional cases

Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue

Koch, S.

Treatment of NPC with miglustat in Germany

Manifestation and diagnosis of NPC disease in Germany

Kohlschmidt, N.

Mutation analysis of the SCN1A gene for suspected Dravet syndrome/GEFS+ – High detection yield, unsatisfactory prognostic value

Kohlschütter, A.

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

Kolb, R.

Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment

Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients

Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up

Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents

Kolzter, K.

Patients with Dravet's syndrome and SCN1A-mutation with a benign course of illness – A case report with 6 patients

König, S.

Partial response to the vagus nerve stimulation in twins with double cortex syndrome

Korall, H.

Screening for pyridoxine dependent epilepsy (PDE) by Tandem Mass Spectrometry (HPLC-MS/MS)

Korenke, C.

Treatment of NPC with miglustat in Germany

Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)

Manifestation and diagnosis of NPC disease in Germany

Korinthenberg, R.

Treatment of Duchenne muscular dystrophy with cyclosporin A – A randomized, double-blind, placebo controlled trial

Severe confusion and agitation as predominant symptom of a hemiplegic migraine with mutation in ATP1A2

Wernicke encephalopathy in childhood

Kornak, U.

Intractable seizures in malignant infantile osteopetrosis due to CLCN7 mutation: lysosomal aspects

Körte, I.

Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia

Kortmann, R.

Low grade glioma in pediatric NF-1 patients

Kortmann, R. D.

Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment

Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up

Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents

Kotzaeridou, U.

Full clinical recovery after acute haemolytic uraemic syndrome (HUS) with basal ganglia involvement and severe dystonia. A case report

Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia

Acute motor and sensory axonal neuropathy (AMSAN) in a 7-year-old boy. A cases report

Atypical clinical presentation of a girl with episodic ataxia type II

Kotzot, D.

Cardiac arrest in a patient with glutaric aciduria type II

Krägeloh-Mann, I.

Clinical course of two siblings with Metachromatic Leukodystrophy (MLD) with and without Stem cell transplantation (SCT)

Neurocysticercosis in a 10 year-old boy in Germany

Diagnostic value of magnetic resonance imaging and morphometry of the corpus callosum in children with isolated mental retardation

A new score for assessing white matter changes in metachromatic leukodystrophy

Early determination of somatosensory cortex

Polyneuropathy and hepatopathy as an infantile manifestation of a POLG1 gene defect

Krätzner, R.

The structure of tripeptidyl peptidase I (TPP1) provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis

Kraus, C.

Accessory nipple as key symptom in diagnosis of Mowat-Wilson syndrome

Krause, M.

Deep brain stimulation in children and adolescents with dystonia

Kress, W.

A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity

Kreuder, J.

Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)

Kribs, A.

Combination of early endotracheal Surfactant and nasal continous positive airwaypressure (CPAP): 15–32-month outcome of extremly low birth weight preterm infants (ELBW)

Krick, C.

Modified memory processes in children with febrile seizures: Analysis of event-related potentials

Krischke, G.

Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)

Kruse, B.

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

Kuczaty, S.

Mutation analysis of the SCN1A gene for suspected Dravet syndrome/GEFS+ – High detection yield, unsatisfactory prognostic value

Kudernatsch, M.

Fast recovery after 5 months in persistent vegetative state

Kuhnke, N.

Does navigated transcranial magnetic stimulation (TMS) decrease the variability of motor evoked potentials (MEP) and increase its reproducibility?

Kunz, W.

Mutation analysis of the SCN1A gene for suspected Dravet syndrome/GEFS+ – High detection yield, unsatisfactory prognostic value

mitoNET – German Network for mitochondrial disorders

Kurlemann, G.

Epilepsy in vitamin B12 deficiency and its treatment in infancy

Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?

Autosomal dominant chin myoclonus

A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity

Kyttällä, A.

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

Laccone, F.

The Preserved Speech Variant of Rett syndrome: Specificity of atypicality?

Lackner, H.

Opsoklonus-Myoklonus-Syndrom

Landgraf, M.

Toxic effects of lamotrigine ingestion in children

Therapy of headaches in children and adolescents with TENS (Transcutaneous Electrical Nerve Stimulation) – An observational study of the Children's Hospital of the University of Leipzig

Chronic fatigue and pain syndrome caused by persistent intoxication with cactus spurge in a 12-year-old girl

Lauffer, H.

Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity

Le, Q.

KCNQ potassium channels are critical determinants of neuronal network activity in neonatal mouse brain

Lebrun, A. H.

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

Ledvinova, J.

GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase

Lehmann-Horn, F.

A rare Ca2+ channel mutation R528G identified in a patient with autosomal dominant hypokalemic periodic paralysis (HypoPP-1)

Lehner, K.

Fast recovery after 5 months in persistent vegetative state

Leiz, S.

Accessory nipple as key symptom in diagnosis of Mowat-Wilson syndrome

Monosomy 9pter-p22 in a boy with neonatal hypoglycemia, epilepsy, facial dysmorphism and hypotonia

Lerche, H.

Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes

Lettau, M.

Neurocysticercosis in a 10 year-old boy in Germany

Limperopoulos, C.

Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia

Lindbichler, F.

Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations

Lindhout, D.

VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data

Logeswaran, T.

Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)

Lombet, A.

Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease

Lorenz, I.

Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report

Lorenz, N.

Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)

Loron, G.

Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease

Lotte, J.

Provocation of seizures by vaccination with children suffering from SCN1A-mutation

Patients with Dravet's syndrome and SCN1A-mutation with a benign course of illness – A case report with 6 patients

Lotze, M.

Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity

Lücke, T.

Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure

M. Scheie: Failure of enzyme replacement therapy to prevent CNS- and spinal-lesions

Ludwig, H. C.

Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency

Luef, G.

Oxcarbazepine accelerates steroid elimination in young men with epilepsy due to cytochrome P450 3A4 induction

Lütjen, S.

Hemiplegic migraine with cerebellar atrophy: A second pediatric case

Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)

Mache, C. J.

Plasmapheresis in the treatment of pediatric patients with neurological diseases: 10 years experience

Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations

Madignier, F.

Improved molecular diagnostics for patients with respiratory chain complex deficiency

Maier, C.

Quantitative Sensory Testing (QST) in children and adolescents

Maier, O.

Citrobacter koseri meningitis – A rare and severe disease in the neonate. A case report

Makowski, C.

Hennekam-syndrome with unusual MRI-changes and symptomatic epilepsy

Mall, V.

Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases

Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up

Does navigated transcranial magnetic stimulation (TMS) decrease the variability of motor evoked potentials (MEP) and increase its reproducibility?

Mantz, J.

Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease

Marquardt, T.

Treatment of NPC with miglustat in Germany

Manifestation and diagnosis of NPC disease in Germany

Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease

Marschik, P. B.

Is there an association between Touwen's neurological examination and the Zuerich neuromotor assessment?

Associated movements in 5- to 10-year-old infants

A possible association between genotypes and early signs of Rett disorder

The Preserved Speech Variant of Rett syndrome: Specificity of atypicality?

Marschitz, I.

20 years evaluation of pediatric patients with encephalitis in the PICU

Plasmapheresis in the treatment of pediatric patients with neurological diseases: 10 years experience

Martelli, M.

Neuropathologic findings in patients with primary autosomal recessive microcephaly

Mayer, H.

Surgery during early life in children with intractable epilepsy – A prospective evaluation

Mayr, H.

Diagnostic strategy in mitochondrial disorders – An update

Mayr, J.

Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue

Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations

Improved molecular diagnostics for patients with respiratory chain complex deficiency

Mayrhofer, H.

Diagnostic value of magnetic resonance imaging and morphometry of the corpus callosum in children with isolated mental retardation

Mecklinger, A.

Modified memory processes in children with febrile seizures: Analysis of event-related potentials

Mehrkens, J. H.

Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia

Meitinger, T.

mitoNET – German Network for mitochondrial disorders

Improved molecular diagnostics for patients with respiratory chain complex deficiency

Clinical characterisation of NBIA patients with and without mutation in PANK2 gene

Mengel, E.

Case report: Rapid evolving, severe encephalopathy, caused by nutritive cobalamin deficiency due to subclinical maternal pernicious anemia

Treatment of NPC with miglustat in Germany

Manifestation and diagnosis of NPC disease in Germany

Merkel, H. J.

Partial response to the vagus nerve stimulation in twins with double cortex syndrome

Merkenschlager, A.

Seizures caused by accidental dimenhydriante intoxication

Toxic effects of lamotrigine ingestion in children

Miller Fisher syndrome and Guillain Barré syndrome with ophtamloplegia: Two cases with overlapping phenotype

Therapy of headaches in children and adolescents with TENS (Transcutaneous Electrical Nerve Stimulation) – An observational study of the Children's Hospital of the University of Leipzig

Chronic fatigue and pain syndrome caused by persistent intoxication with cactus spurge in a 12-year-old girl

Merten, A.

Diagnostic value of magnetic resonance imaging and morphometry of the corpus callosum in children with isolated mental retardation

Meyer, S.

Modified memory processes in children with febrile seizures: Analysis of event-related potentials

The prognostic value of EEG in children with minor head trauma

Meyer-Heim, A.

Robotic-assisted treadmill therapy enhances motor functions in children with bilateral spastic cerebral palsy

Michelakakis, H.

GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase

Miehe, U.

Seizures caused by accidental dimenhydriante intoxication

Moers, A. von

CDKL5 mutation in neonatal onset of epilepsy

Mole, S. E.

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

Möller-Hartmann, C.

Ataxia with oculomotor apraxia 1 (AOA1) in a consanguineous Pakistanian familiy

Moog, U.

Multiple epiphyseal dysplasia as differenzial diagnosis in patients with L-Dopa responsive dystonia

Morass, M.

Proinflamatory cytokines in children with febrile seizures

Morris-Rosendahl, D. J.

Muscular magnet resonance imaging (M-MRI) in α-Dystroglykanopathies – clinical course of two juvenile patients with LGMD2I and LGMD2M

Moser, A.

Opsoklonus-Myoklonus-Syndrom

Motz, R.

Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease

Muckenhaupt, T.

Neonatal encephalitis through human parechoviruses with signs of extensive white matter injury – Case study and comparison to existing published cases

Muhle, H.

Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes

VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data

Müller, A.

Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia

Müller, H. L.

Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment

Peripheral alpha MSH in childhood obesity and craniopharyngioma

Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients

Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up

Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents

Müller, I.

Clinical course of two siblings with Metachromatic Leukodystrophy (MLD) with and without Stem cell transplantation (SCT)

Müller, U.

IAHSP caused by maternal uniparental isodisomy in ALS2

Munk, I.

Partial response to the vagus nerve stimulation in twins with double cortex syndrome

Mütze, U.

Seizures caused by accidental dimenhydriante intoxication

Nagel, A.

Focal dystonia of dominant hand in a 13 year old girl: Action dystonia successfully treated by botulinumtoxine A (Xeomin®)

Multimodal treatment of Cerebral Palsy (CP) including physical therapy, Botulinumtoxin und Lokomat-Training: A case report

Treatment of cerebral palsy: Use of botulinum neurotoxin type A free of complexing proteins (Xeomin®) in childhood

Nagl, A.

Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)

Naxer, S.

Cyclic Esotropia – A rare differenzial diagnosis in non paralytic strabismus in childhood

Neu, A.

KCNQ potassium channels are critical determinants of neuronal network activity in neonatal mouse brain

Neubauer, B.

Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes

Non-invasive tension-time-index and ventilator use in Duchenne muscular dystrophy

Treatment of gastroesophageal reflux with Nissen fundoplication and gastrostomy tube insertion in infantile Pompe's disease

Neuhann, T.

Pontine tegmental cap dysplasia: Two additional cases

Niederstadt, T.

Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?

Niesytto, C.

Outcome of endoscopic therapy of complex hydrocephalus

Nomayo, H. O.

IV Levetiracetam in the management of refractory complex-partial status epilepticus

Continous intrathecal baclofen (cITB) therapy terminates spinal spasms mimicking tonic seizures in a teenager with severe spastic cerebral palsy with total body involvement and cervical dystonia

Northam, G.

Language lateralisation in childhood-onset focal epilepsy: Evidence from fMRI

Oberle, A.

A possible association between genotypes and early signs of Rett disorder

The Preserved Speech Variant of Rett syndrome: Specificity of atypicality?

Obermaier-Kusser, B.

mitoNET – German Network for mitochondrial disorders

Obermeier, T.

Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes

Omran, H.

Severe confusion and agitation as predominant symptom of a hemiplegic migraine with mutation in ATP1A2

Opherk, K.

Clinical course of two siblings with Metachromatic Leukodystrophy (MLD) with and without Stem cell transplantation (SCT)

Opladen, T.

Multiple epiphyseal dysplasia as differenzial diagnosis in patients with L-Dopa responsive dystonia

Oster, I.

The prognostic value of EEG in children with minor head trauma

Pahs, G.

Surgery during early life in children with intractable epilepsy – A prospective evaluation

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Language lateralisation in childhood-onset focal epilepsy: Evidence from fMRI

Pal, A.

The structure of tripeptidyl peptidase I (TPP1) provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis

Pansy, J.

Assessment of spontaneous movements in an infant with Peters anomaly

Is there an association between Touwen's neurological examination and the Zuerich neuromotor assessment?

Associated movements in 5- to 10-year-old infants

Panzer, A.

CDKL5 mutation in neonatal onset of epilepsy

Pape, L.

Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure

Paschke, E.

Imino analogues of galactose: Inhibitors of human acid β-D-Galactosidase and putative pharmacological chaperones for the treatment of GM1-Gangliosidosis

Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation

GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase

Pauen, S.

Self regulation in preterms – preliminary data with regard to the assessment of „Effortful Control“

Paul, K.

Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation

GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase

Peineau, S.

Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease

Penzien, J.

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder

Pernice, W.

Miller Fisher syndrome and Guillain Barré syndrome with ophtamloplegia: Two cases with overlapping phenotype

Petermann, F.

Evaluation of Stepping Stones Triple P – 3-year-interims-analysis of the Stepping-Stones-SPC-Multicenter-Study

Peters, J.

Accessory nipple as key symptom in diagnosis of Mowat-Wilson syndrome

Philippi, H.

Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)

Pietsch, T.

Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment

Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients

Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up

Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents

Low grade glioma in pediatric NF-1 patients

Pietz, J.

Full clinical recovery after acute haemolytic uraemic syndrome (HUS) with basal ganglia involvement and severe dystonia. A case report

Acute motor and sensory axonal neuropathy (AMSAN) in a 7-year-old boy. A cases report

Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)

Self regulation in preterms – preliminary data with regard to the assessment of „Effortful Control“

Pilhatsch, A.

Febrile seizures – First symptom of Rasmussenencephalitis

Plecko, B.

Febrile seizures – First symptom of Rasmussenencephalitis

Abstracts of the 35th Annual Meeting of the Society of Neuropediatrics, „Gesellschaft für Neuropädiatrie“, 23rd to 26th April 2009

Plasmapheresis in the treatment of pediatric patients with neurological diseases: 10 years experience

Opsoklonus-Myoklonus-Syndrom

Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation

Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations

GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase

Homocystein as an important diagnostic marker of remethylation defects – A case report

Pohl, F.

Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment

Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents

Pohlmann-Eden, B.

A series of 34 patients with Rasmussen's encephalitis: Clinical course, EEG- and MRI findings

Poretti, A.

Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia

Pontine tegmental cap dysplasia: Two additional cases

Porsche, B.

Surgery during early life in children with intractable epilepsy – A prospective evaluation

Do children with drug resistant epilepsy and low IQ also improve after epilepsy Ssrgery?

Prayer, D.

Surgery during early life in children with intractable epilepsy – A prospective evaluation

Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia

Prechtl, H. F. R.

A possible association between genotypes and early signs of Rett disorder

Prokisch, H.

Diagnostic strategy in mitochondrial disorders – An update

mitoNET – German Network for mitochondrial disorders

Improved molecular diagnostics for patients with respiratory chain complex deficiency

Clinical characterisation of NBIA patients with and without mutation in PANK2 gene

Prokop, K.

Postinfectious autoimmune-mediated encephalitis versus relapse of herpes encephalitis?

Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report

Rankin, P.

Language lateralisation in childhood-onset focal epilepsy: Evidence from fMRI

Rapp, E. M.

Is there an association between Touwen's neurological examination and the Zuerich neuromotor assessment?

Rascher, W.

Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)

Rating, D.

GLUT1 deficiency in a child with a movement disorder

Rauchenzauner, M.

Oxcarbazepine accelerates steroid elimination in young men with epilepsy due to cytochrome P450 3A4 induction

Proinflamatory cytokines in children with febrile seizures

Rauscher, C.

Treatment of West syndrome (WS) according to UKISS (United Kindom Infantile Spasms Study): A single centers experience

Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia

Pontine tegmental cap dysplasia: Two additional cases

Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue

GLUT1 deficiency syndrome – A novel phenotype and a novel mutation

Reinehr, T.

Peripheral alpha MSH in childhood obesity and craniopharyngioma

Reinhardt, K.

Cyclic Esotropia – A rare differenzial diagnosis in non paralytic strabismus in childhood

Reiser, M.

Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia

Reissig, A.

Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up

Reiter, E.

Surgery during early life in children with intractable epilepsy – A prospective evaluation

Reiter-Fink, E.

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Reith, W.

Modified memory processes in children with febrile seizures: Analysis of event-related potentials

Reithofer, E.

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Reuner, G.

Self regulation in preterms – preliminary data with regard to the assessment of „Effortful Control“

Reutlinger, C.

Rufinamide treatment in 18 patients with Lennox-Gastaut syndrome – Documentation with the electronic patient diary epivista®

Rhein, M. von

Case report: Rapid evolving, severe encephalopathy, caused by nutritive cobalamin deficiency due to subclinical maternal pernicious anemia

Long-term antikoagulation in a neonate with sinovenous thrombosis and stroke. Case presentation and review of the literature

Richter, J. W.

Pyridoxine dependent epileptic encephalopathy mimicking neonatal abstinence syndrome – a case report with video documentation

Ring, E.

Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations

Rittinger, O.

Intractable seizures in malignant infantile osteopetrosis due to CLCN7 mutation: lysosomal aspects

Rödl, S.

20 years evaluation of pediatric patients with encephalitis in the PICU

Plasmapheresis in the treatment of pediatric patients with neurological diseases: 10 years experience

Rohrbach, M.

Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development

Rolinski, B.

Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue

Diagnostic strategy in mitochondrial disorders – An update

Improved molecular diagnostics for patients with respiratory chain complex deficiency

Roos, R.

Intracerebral calcification in a newborn – Not always a connatal infection

Rosewich, H.

Cerebral MRI as a valuable tool for the diagnosis of Zellweger syndrome spectrum patients and patients with peroxisomal β-oxidation defects

Rostasy, K.

Uncommon manifestations of childhood neuroborreliosis

Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)

Rostásy, K.

Proinflamatory cytokines in children with febrile seizures

Roth, C. L.

Peripheral alpha MSH in childhood obesity and craniopharyngioma

Roulet-Perez, E.

Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia

Rutsch, F.

Treatment of NPC with miglustat in Germany

Manifestation and diagnosis of NPC disease in Germany

Sanchez-Albisua, I.

Diagnostic value of magnetic resonance imaging and morphometry of the corpus callosum in children with isolated mental retardation

Santer, R.

GLUT1 deficiency in a child with a movement disorder

Sassen, R.

Provocation of seizures by vaccination with children suffering from SCN1A-mutation

Mutation analysis of the SCN1A gene for suspected Dravet syndrome/GEFS+ – High detection yield, unsatisfactory prognostic value

Schaadt, A. K.

Evaluation of Stepping Stones Triple P – 3-year-interims-analysis of the Stepping-Stones-SPC-Multicenter-Study

Schallner, J. C.

A rare Ca2+ channel mutation R528G identified in a patient with autosomal dominant hypokalemic periodic paralysis (HypoPP-1)

Schaper, J.

Copper histidine therapy started in a boy at the age of three years – Treatment option for a mild form of Menkes's disease

Schara, U.

Copper histidine therapy started in a boy at the age of three years – Treatment option for a mild form of Menkes's disease

Ataxia with oculomotor apraxia 1 (AOA1) in a consanguineous Pakistanian familiy

Scheer, I.

Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development

Scheffer, H.

GLUT1 deficiency syndrome – A novel phenotype and a novel mutation

GLUT1 deficiency syndrome in a consanguineous Arab family carrying a novel homozygous missense mutation

Scheffner, T.

Neonatal encephalitis through human parechoviruses with signs of extensive white matter injury – Case study and comparison to existing published cases

Schell-Apacik, C.

CDKL5 mutation in neonatal onset of epilepsy

Schenk, W.

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder

Schessl, J.

Treatment of Duchenne muscular dystrophy with cyclosporin A – A randomized, double-blind, placebo controlled trial

Schilling, S.

Tumor induced Hemichorea

Schimmel, M.

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder

Schitter, G.

Imino analogues of galactose: Inhibitors of human acid β-D-Galactosidase and putative pharmacological chaperones for the treatment of GM1-Gangliosidosis

Schittkowski, M.

Cyclic Esotropia – A rare differenzial diagnosis in non paralytic strabismus in childhood

Schlachter, K.

Posterior reversible encephalopathy syndrome (PRES)

Schlee-Böckh, K.

Long-term antikoagulation in a neonate with sinovenous thrombosis and stroke. Case presentation and review of the literature

Schlotawa, L.

Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency

Schmitt, C. P.

Full clinical recovery after acute haemolytic uraemic syndrome (HUS) with basal ganglia involvement and severe dystonia. A case report

Schneider, C.

Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)

Scholl-Buergi, S.

Proinflamatory cytokines in children with febrile seizures

Scholl-Bürgi, S.

Cardiac arrest in a patient with glutaric aciduria type II

Schöls, L.

mitoNET – German Network for mitochondrial disorders

Schöning, M.

The development of cerebral perfusion during the first three years of life: Long-term follow-up study of cerebral blood flow volume measurement in two healthy children

Schramm, P.

Ophthalmoplegic migraine (OM) with early-onset recurrent oculomotor palsy of the left eye in a 6-year-old boy

Schranz, D.

Severe dilative Cardiomyopathy in mucopolysaccharidosis type 1 (Hurler's Syndrome)

Schreiber, S.

Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes

Schröder, A. S.

Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases

Schröder, H. W. S.

Outcome of endoscopic therapy of complex hydrocephalus

Schröder, S.

Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment

Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients

Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up

Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents

Schröder, S. A.

Safety of botulinum toxin treatment in children with cerebral palsy in correlation to GMFCS level

Correlation of botulinum toxin dosage and GMFCS level in children with bilateral spastic cerebral palsy – An explorative cohortstudy

Schülke-Gerstenfeld, M.

mitoNET – German Network for mitochondrial disorders

Schulz, A.

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

Schulz, M.

Miller Fisher syndrome and Guillain Barré syndrome with ophtamloplegia: Two cases with overlapping phenotype

Schwartz, O.

Epilepsy in vitamin B12 deficiency and its treatment in infancy

Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?

Autosomal dominant chin myoclonus

A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity

Schweiger, B.

Copper histidine therapy started in a boy at the age of three years – Treatment option for a mild form of Menkes's disease

Schwinger, W.

Opsoklonus-Myoklonus-Syndrom

Seidl, R.

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Deep-brain stimulation in a boy with DYT1 dystonia

Seitz, A.

Full clinical recovery after acute haemolytic uraemic syndrome (HUS) with basal ganglia involvement and severe dystonia. A case report

Sengupta, D.

Hashimoto's encephalopathy with stroke-like episodes and optic neuritis in a 19-year-old patient

Sergi, C.

Cardiac arrest in a patient with glutaric aciduria type II

Shamdeen, M. G.

Modified memory processes in children with febrile seizures: Analysis of event-related potentials

The prognostic value of EEG in children with minor head trauma

Sheldrick, G.

The structure of tripeptidyl peptidase I (TPP1) provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis

Siegler, N.

Severe generalized neuropathy in an 18-year-old patient with hereditary sensory-motor polyneurpathy (HMSN) type 1 treated with vincristine due to acute leukemia

Sifringer, M.

Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission

Smitka, M.

Postinfectious autoimmune-mediated encephalitis versus relapse of herpes encephalitis?

Muscular magnet resonance imaging (M-MRI) in α-Dystroglykanopathies – clinical course of two juvenile patients with LGMD2I and LGMD2M

Sorantin, E.

20 years evaluation of pediatric patients with encephalitis in the PICU

Sörensen, N.

Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment

Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients

Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up

Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents

Sperl, W.

Relevance of functional investigations of the mitochondrial energy metabolism in unfrozen tissue

Diagnostic strategy in mitochondrial disorders – An update

Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations

Improved molecular diagnostics for patients with respiratory chain complex deficiency

Spiczak, S. von

Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes

VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data

Sprinz, A.

Focal dystonia of dominant hand in a 13 year old girl: Action dystonia successfully treated by botulinumtoxine A (Xeomin®)

Multimodal treatment of Cerebral Palsy (CP) including physical therapy, Botulinumtoxin und Lokomat-Training: A case report

Treatment of cerebral palsy: Use of botulinum neurotoxin type A free of complexing proteins (Xeomin®) in childhood

Stark, W.

Natalizumab in 4 cases of pediatric multiple sclerosis

Staudt, M.

Hemiplegic migraine with cerebellar atrophy: A second pediatric case

Early determination of somatosensory cortex

Stefovska, V. G.

Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission

Steichen-Gersdorf, E.

Cardiac arrest in a patient with glutaric aciduria type II

Steinborn, M.

Hennekam-syndrome with unusual MRI-changes and symptomatic epilepsy

Steinfeld, R.

Hydrocephalus as a rare clinical symptom in a patient with multiple sulfatase deficiency

The structure of tripeptidyl peptidase I (TPP1) provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis

Steinlin, M.

Bannwarth's syndrome – A rare but important manifestation of neuroborreliosis in childhood

Therapy of sinus venous thrombosis in childhood – A standardised treatment protocol – Call for participation

Stenger, R. D.

Outcome of endoscopic therapy of complex hydrocephalus

Stephani, U.

Rufinamide treatment in 18 patients with Lennox-Gastaut syndrome – Documentation with the electronic patient diary epivista®

Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes

VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data

Stöcklin, B.

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Stolle, S.

Does navigated transcranial magnetic stimulation (TMS) decrease the variability of motor evoked potentials (MEP) and increase its reproducibility?

Stoltenburg-Didinger, G.

Neuropathologic findings in patients with primary autosomal recessive microcephaly

Storch, S.

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

Stötter, M.

Polyneuropathy and hepatopathy as an infantile manifestation of a POLG1 gene defect

Strobl, R.

Uncommon manifestations of childhood neuroborreliosis

Stülpnagel, C. von

Intracerebral calcification in a newborn – Not always a connatal infection

Stupp, N.

Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?

Stütz, A.

Imino analogues of galactose: Inhibitors of human acid β-D-Galactosidase and putative pharmacological chaperones for the treatment of GM1-Gangliosidosis

Syrbe, S.

Seizures caused by accidental dimenhydriante intoxication

Toxic effects of lamotrigine ingestion in children

Miller Fisher syndrome and Guillain Barré syndrome with ophtamloplegia: Two cases with overlapping phenotype

Therapy of headaches in children and adolescents with TENS (Transcutaneous Electrical Nerve Stimulation) – An observational study of the Children's Hospital of the University of Leipzig

Chronic fatigue and pain syndrome caused by persistent intoxication with cactus spurge in a 12-year-old girl

Tacke, U.

Wernicke encephalopathy in childhood

Taeuber, A.

Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?

Telegravciska, M.

Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia

Tesarova, M.

Improved molecular diagnostics for patients with respiratory chain complex deficiency

Thoms, K.

Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity

Timmann-Braun, D.

Ataxia with oculomotor apraxia 1 (AOA1) in a consanguineous Pakistanian familiy

Tinschert, S.

Pontine tegmental cap dysplasia: Two additional cases

Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report

Trefz, F. K.

Neonatal encephalitis through human parechoviruses with signs of extensive white matter injury – Case study and comparison to existing published cases

Trimmel-Schwahofer, P.

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Tro-Baumann, B.

Provocation of seizures by vaccination with children suffering from SCN1A-mutation

Trollmann, R.

Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report

Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)

Tsiakas, K.

Treatment of NPC with miglustat in Germany

Manifestation and diagnosis of NPC disease in Germany

Tuglaci, S.

Modified memory processes in children with febrile seizures: Analysis of event-related potentials

Turski, L.

Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission

Tyshchenko, N.

Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report

Uhl, M.

Wernicke encephalopathy in childhood

Uhlig, H.

Seizures caused by accidental dimenhydriante intoxication

Ullrich, K.

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

Urak, L.

Surgery during early life in children with intractable epilepsy – A prospective evaluation

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Utzig, N.

Insights into the regulation of eating behavior: fMRI, peripheral physiology and multichannel EEG in children and adolescents with obesity

van Baalen, A.

VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data

van Kempen, M. J. A.

VACENC – A retrospective and prospective study of clinical and genetic characteristics of vaccine encephalopathies: preliminary clinical data

Vargha-Khadem, F.

Language lateralisation in childhood-onset focal epilepsy: Evidence from fMRI

Vass, K.

Epidemiology of pediatric multiple sclerosis in Austria

Vater, D.

Hashimoto's encephalopathy with stroke-like episodes and optic neuritis in a 19-year-old patient

Acute motor and sensory axonal neuropathy (AMSAN) in a 7-year-old boy. A cases report

Deep brain stimulation in children and adolescents with dystonia

IAHSP caused by maternal uniparental isodisomy in ALS2

GLUT1 deficiency in a child with a movement disorder

Verney, C.

Microglia express functional NMDA receptors: A novel finding and a promise for innovative treatment of excitotoxic and inflammatory brain disease

Vester, U.

Copper histidine therapy started in a boy at the age of three years – Treatment option for a mild form of Menkes's disease

Vianey-Saban, C.

Cardiac arrest in a patient with glutaric aciduria type II

Vincent, A.

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder

Vogrinec, G.

The Preserved Speech Variant of Rett syndrome: Specificity of atypicality?

Voigt, B.

Self regulation in preterms – preliminary data with regard to the assessment of „Effortful Control“

Wagenstaller, J.

Monosomy 9pter-p22 in a boy with neonatal hypoglycemia, epilepsy, facial dysmorphism and hypotonia

Waibel, P.

Citrobacter koseri meningitis – A rare and severe disease in the neonate. A case report

Walden, U.

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder

Walkinshaw, G.

Modulation of vasoactive and cytotrophic factors in developing mouse brain by pharmacological stabilization of hypoxia-inducible transcription factors (HIFs)

Waltz, S.

Patients with Dravet's syndrome and SCN1A-mutation with a benign course of illness – A case report with 6 patients

Warmuth-Metz, M.

Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment

Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients

Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up

Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents

Low grade glioma in pediatric NF-1 patients

Weber, P.

Acute disseminated encephalomyelitis review in 8 pediatric patients

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Weber, Y.

Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes

Wedekin, M.

Neurodevelopmental follow-up of school-age children with congenital kidney disease and consecutive chronic renal failure

Weglage, J.

Focal dystonia of dominant hand in a 13 year old girl: Action dystonia successfully treated by botulinumtoxine A (Xeomin®)

Treatment of cerebral palsy: Use of botulinum neurotoxin type A free of complexing proteins (Xeomin®) in childhood

Wehrli, E.

Therapy of sinus venous thrombosis in childhood – A standardised treatment protocol – Call for participation

Weigel, C.

Outcome of endoscopic therapy of complex hydrocephalus

Weise, A.

Monosomy 9pter-p22 in a boy with neonatal hypoglycemia, epilepsy, facial dysmorphism and hypotonia

Weise, D.

Cyclic Esotropia – A rare differenzial diagnosis in non paralytic strabismus in childhood

Weise, S.

Sandifers syndrome – Unusual case report and review of the literature

Dystonic movements and developmental coordination disorder – Successful treatment with methylphenidate

Weissert, M.

Citrobacter koseri meningitis – A rare and severe disease in the neonate. A case report

Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia

Acute basilar artery thrombosis in childhood: A therapeutic dilemma

Outcome of acute peripheral facial palsy in children – A catamnestic study of 84 patients

Wendelin, G.

Febrile seizures – First symptom of Rasmussenencephalitis

Homocystein as an important diagnostic marker of remethylation defects – A case report

Wenzel, D.

Fractionated stereotactic radiosurgery of a large intracranial arteriovenous malformation (AVM) – A case report

Westhoff, B.

Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up

Wiegand, C.

Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment

Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients

Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up

Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents

Wilke, M.

Clinical course of two siblings with Metachromatic Leukodystrophy (MLD) with and without Stem cell transplantation (SCT)

A new score for assessing white matter changes in metachromatic leukodystrophy

Winter, P.

IAHSP caused by maternal uniparental isodisomy in ALS2

Wittig, I.

mitoNET – German Network for mitochondrial disorders

Wochner, K.

Looking at General Movements (GM) with a computer-aided approach. First results of a study in progress on the early detection of infantile cerebral palsy (ICP)

Woermann, F.

A series of 34 patients with Rasmussen's encephalitis: Clinical course, EEG- and MRI findings

Wolf, N.

Full clinical recovery after acute haemolytic uraemic syndrome (HUS) with basal ganglia involvement and severe dystonia. A case report

Deep brain stimulation in children and adolescents with dystonia

IAHSP caused by maternal uniparental isodisomy in ALS2

GLUT1 deficiency in a child with a movement disorder

Atypical clinical presentation of a girl with episodic ataxia type II

Wolf, N. I.

Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia

Wrodnigg, T.

Imino analogues of galactose: Inhibitors of human acid β-D-Galactosidase and putative pharmacological chaperones for the treatment of GM1-Gangliosidosis

Wudy, S.

Oxcarbazepine accelerates steroid elimination in young men with epilepsy due to cytochrome P450 3A4 induction

Zabel, C.

Long-term effects on the developing brain through a brief alteration of NMDA or GABAA receptor mediated neurotransmission

Zeiner, F.

Hemiplegic migraine with cerebellar atrophy: A second pediatric case

Zernikow, B.

Quantitative Sensory Testing (QST) in children and adolescents

Zobel, G.

20 years evaluation of pediatric patients with encephalitis in the PICU

Plasmapheresis in the treatment of pediatric patients with neurological diseases: 10 years experience

Zotter, S.

Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)

Zürcher, C.

Natalizumab in 4 cases of pediatric multiple sclerosis

Zwiener, I.

Randomized multicenter trial on patients wit childhood craniopharyngioma (KRANIOPHARYNGEOM 2007) – Update after 12 months of recruitment

Meningiomas in childhood and adolescence – Multicenter cross-sectional study on 42 patients

Analyses of treatment variables for patients with childhood craniopharyngioma – Results of the multicenter prospective trial KRANIOPHARYNGEOM 2000 after three years of follow-up

Xanthogranuloma of the sellar region – Results of a multicenter prospective study on diagnostics, therapy and prognosis in children and adolescents

Zwirner, A.

Neuropathologic findings in patients with primary autosomal recessive microcephaly