Abstracts of the 41st Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) Autorenliste

Gärtner, J.

Bone Marrow Transplantation in a Mouse Model for Rett Syndrome

Gattinger, N.

Transcranial Biphasic Quadro-Pulse Stimulation with One but not Two Full-Sine Cycles Induces Long-Term Depression-Like Changes in Corticomotor Excitability

Gburek-Augustat, J.

Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study

Geis, T.

Genotype and Phenotype in 34 Families with Genetically Confirmed Walker-Warburg Syndrome or Muscle Eye Brain Disease
Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly

Gleich, B.

Transcranial Biphasic Quadro-Pulse Stimulation with One but not Two Full-Sine Cycles Induces Long-Term Depression-Like Changes in Corticomotor Excitability

Gleixner, E.

Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases

Glöckle, N.

Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases

Gloor, M.

Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin

Göpel, W.

Very Low Birth Weight Infants in Germany: How many Therapies Do They Get until Preschool Age?

Graness, I.

Therapy and Clinical Course in 52 Patients with PCDH19 Mutations

Grange, D.

Brain Stem Disconnection: Two Additional Patients and Expansion of the Phenotype

Granström, S.

Executive Dysfunction in Neurofibromatosis Type 1: Comparison to Idiopathic ADHD

Grau, T.

Comprehensive NGS-Based Diagnostics in over 800 Patients with Epileptic Encephalopathy
Diagnostic Panels: A Powerful Tool to Identify the Underlying Genetic Cause in Neuromuscular Diseases

Greulich, N.

Becker Muscular Dystrophy in a 2-Year-Old Boy caused by a Novel Missense Mutation p.Arg145Pro in the Dystrophin Gene

Gröschel, S.

Intrafamilial Variability of Natural Disease Course in Metachromatic Leukodystrophy

Groß, C.

Predictive Value of Cerebrospinal Fluid Flow Cytometry in Pediatric Multiple Sclerosis

Groß, M.

Cerebral Palsy and Breathing: More than Prophylaxis of Pneumonia

Grosse, R.

Optic Atrophy in an Iron Storage Disorder Reducing Tissue Iron Load in a Child with MPAN Disease

Große-Opphoff, J.

Never Trust a Normal MRI

Grosser, K.

Olfactory Function in Head Trauma Patients a Link to Frontal Brain Damage?

Gruber-Sedlmayr, U.

Neuralgic Amyotrophy: A Rare Disease in Adolescence

Grunt, S.

Pontocerebellar Hypoplasia Type 9: A New Subtype
Quality of Life 5 Years after Neonatal Arterial Ischemic Stroke: Is there an Association with Hand Motor Performance?
Longitudinal Functional Reorganization after Pediatric Stroke: A Descriptive Case Study
Muscle Contractures in Children with Spastic Cerebral Palsy
LPIN1 Mutations are an Important Cause of Rhabdomyolysis

Guerrini, R.

Therapy and Clinical Course in 52 Patients with PCDH19 Mutations

Gusek-Schneider, G.

Rare Variant of GM2 Gangliosidosis due to Activator Protein Deficiency: A Case Report

Guzman, R.

Arrested Hydrocephalus in Children: Report of Five Consecutive Cases and Comprehensive Review of the Literature