Abstracts of the 31st Annual Meeting of the Society for Neuropediatrics (Gesellschaft für Neuropädiatrie)

Abstracts (HTML) List of Authors

Sälke-Kellermann, R. A.

Loss of consciousness, “dysrhythmic EEG“, epilepsy in the familial history – but no epilepsy!

Salomons, G. S.

Clinical and molecular features of a boy with incomplete WAGR syndrome and succinic semialdehyde dehydrogenase deficiency

Sander, T.

Genomewide linkage scan of the photoparoxysmal response (PPR) and exploration of its relationship to Idiopathic Generalised Epilepsies (IGE)

Sass, J. O.

Clinical and molecular features of a boy with incomplete WAGR syndrome and succinic semialdehyde dehydrogenase deficiency

Sasse, B.

Giant Axonal Neuropathy – a neurodegenerative disorder – a novel mutation in the GAN-Gen

Sasse, M.

Cerebral imaging of CNS involvement in haemolytic uraemic syndrome

Sauter, S.

Chronic inflammatory polyneuropathy as an early symptom of metachromatic leukodystrophy: two case reports

Sayer, J. A.

Confirmation of the JBTS3 locus and identification of a new ahi1 gene mutation in Joubert syndrome (JS) type 3 with renal involvement – evidence for other JS-causing genes in this region?

Schächtele, M.

Parry-Romberg-Syndrom and Rasmussen-encephalitis: A case report

Schäfer, K.

Effects on walking performance of a ten-day treadmill training scheme in children with cerebral palsy

Schara, U.

Genetic analysis of congenital myasthenic syndromes (CMS)
Congenital myasthenic syndromes – variability of symptoms, importance of a final diagnosis

Scheffner, T.

Episodic encephalopathy with coma as the presenting symptom of Hashimoto's encephalopathy

Scheithauer, S.

Herpesvirus infections: an important cause of pediatric hippocampal sclerosis
Cerebral Epstein-Barr Virus (EBV) infection: From human disease to an animal model

Scheld, M.

Significant reduction of muscle diameter after Botulinum Toxin injection in gastrocnemius muscle in children with cerebral palsy

Scherg, M.

Comparison of interictal EEG and MEG II: Loss of deep cortical fissures in polymicrogyria requires simultaneous EEG with MEG source analysis

Schessl, J.

Clinical trial 'immunosuppressive treatment in Duchenne muscular dystrophy' – update

Schlöglhofer, M.

Children with autism: A pilot treatment trial with fishoil EPA/DHA. Evaluation of symptom change and changes in PUFAs after supplementation – a randomised double blind, placebo-controlled pilot study

Schmitz, B.

Genomewide linkage scan of the photoparoxysmal response (PPR) and exploration of its relationship to Idiopathic Generalised Epilepsies (IGE)

Schneider, S.

High-dose, pulsatile steroid-therapy in refractory epilepsies of infancy

Schnöbel, E.

Structured cooperation of neuropediatrics and pediatric psychiatry – why?

Scholl-Bürgi, S.

Chronic inflammatory polyneuropathy as an early symptom of metachromatic leukodystrophy: two case reports
Pyridoxine-responsive seizures in a patient with infantile hypophosphatasia

Schöning, M.

Functional and morphological basics of early brain development

Schreiber, S.

Phenotype-genotype correlation and genetic epidemiology of epilepsy, febrile seizures and neonatal seizures in a defined nothern German region – “popgen-epilepsy“

Schreiner, A.

Topiramate in children and adolescents with epilepsy

Schröder, A. S.

Significant reduction of muscle diameter after Botulinum Toxin injection in gastrocnemius muscle in children with cerebral palsy

Schroeder, A. S.

Experiences with the Assisted Hand Assessment (AHA) in children with cerebral palsy under treatment with botulinum toxin A

Schroeder, S.

Expression of procollagen I, III und IV and their regulators in muscles of children with Cerebral Palsy (CP)

Schropp, C.

Neonatal seizures, lissencephaly and abnormal genitalia – a case of XLAG-syndrome

Schuelke, M.

Molecular diagnostics of mitochondrial encephalomyopathies

Schulze-Bonhage, A.

Seven years of epilepsy surgery in Freiburg: Results of surgery in 100 children 1–16 years of age

Schulz-Schaeffer, W.

TorsinA and B expression in the brain is detectable in human infants as young as four weeks old

Schütz, B.

Spastic paraparesis caused by cerebrovascular neuroborreliosis in a 13-year-old boy

Schwerin, A.

NF-walker and botulinum toxin therapy for children with spastic tetraparesis
Botulinum toxin injections into psoas muscle – effect on leg lengthening in children with spastic hemiparesis

Schwieger, A.

Absence of growth hormone in a child with cat-eye syndrome

Seidel, U.

Cognitive functioning after stroke in childhood – a clinical study

Seidl, R.

Difficult to treat temporal lobe seizures during human parvovirus B19 encephalitis in a 3 5/12-year-old immunocompetent girl – a case report

Seiler-Kramer, B.

Effects on walking performance of a ten-day treadmill training scheme in children with cerebral palsy

Seitz, A.

Comparison of interictal EEG and MEG II: Loss of deep cortical fissures in polymicrogyria requires simultaneous EEG with MEG source analysis

Sellhaus, B.

Herpesvirus infections: an important cause of pediatric hippocampal sclerosis
Cerebral Epstein-Barr Virus (EBV) infection: From human disease to an animal model

Siebler, M.

Physiology and pathophysiology of polyols

Siegert, S.

TorsinA and B expression in the brain is detectable in human infants as young as four weeks old

Simbrunner, J.

Cooper concentration of liver tissue under cooper histidin therapy in a patient with Menkes disease

Simpson, M.

Hereditary spastic paraplegia with thin corpus callosum – childhood onset in two patients

Skladal, D.

Chronic inflammatory polyneuropathy as an early symptom of metachromatic leukodystrophy: two case reports

Smitka, M.

Cardiac and motor improvement with enzyme replacement therapy in a patient with infantile-onset Pompe disease

Sperl, W.

Therapeutic options in mitochondrial encephalomyopathies

Sperner, J.

Rapid onset of cortical hemiatrophy and hippocampal sclerosis after prolonged febrile seizure
Direct EEG changes during Vagus Nerve Stimulation comparing on and off time in children with pharmacoresistant epilepsy
Encephalomyelitis disseminata in a child with severe outcome and atypical clinical findings – Neuromyelitis optica Devic or multiple sclerosis?
Phenotypic variants in children with subtle chromosomal rearrangements
Vagus nerve stimulation in pharmacoresistant epilepsy of childhood and adolescence
Association of Epstein-Barr virus (EBV) infection with multiple sclerosis in pediatric patients

Spiegler, J.

Possible central nervous graft-versus-host reaction after stem cell transplantation by chronic myeloid leukemia

Springer, S.

Structured cooperation of neuropediatrics and pediatric psychiatry – why?

Staudt, M.

Hemispheric dissociation between motor and sensory hand representations in congenital hemiparesis: TMS, fMRI, MEG
Presurgical motor fMRI in a 3-year-old child
Case report: Congenital mirror movements in a 12-year-old girl. Clinical and neurophysiological findings

Stein, S.

Evaluation of BTX/A therapy in children with CP: GMFM-88 vs. GMFM-66

Steinfeld, R.

Functional consequence and clinical importance of distinct mutations in CLN2, the gene associated with classical late infantile ceroid lipofuscinosis

Steinlin, M.

Cognitive functioning after stroke in childhood – a clinical study

Stephani, U.

Phenotype-genotype correlation and genetic epidemiology of epilepsy, febrile seizures and neonatal seizures in a defined nothern German region – “popgen-epilepsy“
Genomewide linkage scan of the photoparoxysmal response (PPR) and exploration of its relationship to Idiopathic Generalised Epilepsies (IGE)
High resolution micro-ultrasound in neuromuscular disorders
Pharmakoresistence – view of the clinician

Stettner, G.

Functional consequence and clinical importance of distinct mutations in CLN2, the gene associated with classical late infantile ceroid lipofuscinosis

Stoltenburg-Didinger, G.

Acute reversible muscle weakness in two infants with limb girdle muscular dystrophy (LGMD) 2I and identification of a novel missense mutation in the FKRP gene

Strassburg, H. M.

Recurrent axonal polyneuropathy with or without alterations of the basal ganglia – a new clinical manifestation of mitochondriopathy?

Straßburg, H. M.

Neonatal seizures, lissencephaly and abnormal genitalia – a case of XLAG-syndrome

Strauch, K.

Genomewide linkage scan of the photoparoxysmal response (PPR) and exploration of its relationship to Idiopathic Generalised Epilepsies (IGE)

Strobl, K.

Seven years of epilepsy surgery in Freiburg: Results of surgery in 100 children 1–16 years of age

Stülpnagel Frfr von Oefele, C. von

Add-on therapy of Levetiracetam (LEV) in difficult-to-treat idiopathic focal epilepsies

Süß, P.

Botulinum toxin injections into psoas muscle – effect on leg lengthening in children with spastic hemiparesis