Abstracts (HTML) List of Authors

Galiart, E.

Biotin Thiamine Responsive Basal Ganglia Disease: Clinical Improvement after Initiation of Biotin and Thiamine Therapy
Infantile Dystonia Parkinsonism Caused by a Mutation in SLC6A3: Case Report of Three Siblings

Galka, A.

Evaluation of the Effects of Anticonvulsive Therapy in Children with Symptomatic Epilepsy by a State Space Modeling Approach

Gallati, S.

Northern Epilepsy: Not So Northern Anymore

Garbade, S. F.

Quantitative Clinical Characteristics of 53 Patients with MPS VII: A Cross-Sectional Analysis

Gärtner, J.

Disease Spectrum of Early-Onset Neurodegeneration
Acute and Episodic Movement Disorders: ATP1A3-Related Disorders as Differential Diagnosis
Effect of Modern Therapy on Disease Progression in Pediatric MS

Gaspar, H.

Leigh Syndrome Caused by a Novel Gene Variant in NDUFS8

Gbadamosi, J.

Guillain-Barré syndrome: Two Cases with Serious and Atypical Process

Gburek-Augustat, J.

Hyperkinetic Movement Disorder as First Manifestation of an Autoimmune Disease
Transcobalamin II Deficiency: Rare Differential Diagnosis in a Neonate with Hematological Disease and Failure to Thrive

Gebhard, B.

Reintegration to School after Craniocerebral Injury: Results of a Survey

Gebhardt, B.

Renal Stones under Antiepileptic Treatment: Pathogenesis and Therapy

Gedik, A.

Perampanel Add-on Therapy for the Treatment of Children and Adolescents with Partial and Primary Generalized Seizures: A Report from the University Hospital of Innsbruck

Gehrlich, C.

Explorative Saccade Training in Children with Homonymous Hemianopia

Geigenberger, C.

Learning to Cope with Mirror Movements in Activities of Daily Living: Effects of Targeted Bimanual Therapy in Children with Unilateral Spastic CP

Gerstl, L.

Improving the Quality of Care in the Specialization: The Benefits of “Hands-on” Courses for Learning Neuromuscular Ultrasound

Gheuens, S.

Interim Efficacy and Safety Results from the Phase 3 ENDEAR Study of Nusinersen in Infants Diagnosed with Spinal Muscular Atrophy (SMA)

Gheuens, Sarah

Efficacy and safety of nusinersen in children with later-onset spinal muscular atrophy (SMA): results of the phase 3 CHERISH study

Gierthmühlen, M.

Progressive Radial Motor Neuropathy Due to a Perineurioma in an Adolescent Girl: Case Report

Goebel, A.-M.

Motor Function in Pediatric ALL Survivors after Chemotherapy-Only

Goerlach, J.

The Impact of Morphometric Skin Punch Biopsy Analysis for a Small Nerve Fiber Involvement in Children with Pain Syndrome

Gormley, M.

Abobotulinumtoxin-A (DYSPORT) Injection Doses per Muscle in Pediatric Patients with Lower Limb Spasticity

Graf, J.

CNV Detection from Targeted Next-Generation Panel Sequencing Data Increases the Diagnostic Yield in Patients with Neuromuscular Diseases

Grandoulier, A. S.

Time to Retreatment after AbobotulinumtoxinA (Dysport) Injections in Children with Dynamic Equinus Foot Deformity
Abobotulinumtoxin-A (DYSPORT) Injection Doses per Muscle in Pediatric Patients with Lower Limb Spasticity

Granström, S.

ADHD Is a Risk Factor for Cognitive Development in NF1

Gratzki, N.

Compound Heterozygous RYR1 Mutation in a Preterm with Arthrogryposis and Core Myopathy with Prenatal CNS Bleedings

Grigull, L.

Long-Term Neurodevelopmental Outcome of Patients with Mucopolysaccharidosis-1H (MPS-1H) following Hematopoietic Stem Cell Transplantation (HSCT)

Grimm, A.

Early Effects after Hematopoietic Stem Cell Transplantation in 13 Children with Juvenile Metachromatic Leukodystrophy

Groeschel, S.

Treating the Brain: The Model of MLD
Remarkable Genetic Finding in a Girl with Phenotype of Classic Pelizäus-Merzbacher Disease: Xq22.2 Microdeletion Including PLP1 and Other Genes
Early Effects after Hematopoietic Stem Cell Transplantation in 13 Children with Juvenile Metachromatic Leukodystrophy

Groß, C.

The Enemy Within: Deleterious Consequences of an Inappropriate Antiviral Response for the Central Nervous System

Groß, S.

Congenital Hyperekplexia: A Visual Diagnosis

Grosser, M.

Longitudinal 8-year Brain Volumetric Analysis in 35 CLN3 Patients: Successful Development of a Sensitive Marker to Measure Clinical Outcome

Gruber-Sedlmayr, U.

4H Leukodystrophy: A Rare Movement Disorder

Gruning, G.

Novel Homozygous Missense Mutation in ALDH7A1 Causes Neonatal Pyridoxine-Dependent Epilepsy

Grunt, S.

Transient Ischemic Attack (TIA): A Problem Not to Miss

Grzybowski, M.

Myositis-Associated Autoantibodies in Juvenile Dermatomyositis
STAC3-Associated Congenital Myopathy in a Boy of Turkish Ancestry with Severe Scoliosis and Early-Onset Respiratory Insufficiency
Congenital Hyperekplexia: A Visual Diagnosis

Günther, L.

Everolimus as a Therapy of a Benign, Infiltrative Growing Bone Tumor of the Mandibula: A Rare Manifestation with Tuberous Sclerosis

Gururangan, S.

Expert Opinion on the Management of Intracerebroventricular (ICV) Drug Delivery