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