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

Abstracts (HTML) List of Authors

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