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Faignart, Nicole
FV 571. Cardiac Kids with Stroke
Falkenstein, Michael
P 235. Short-Term Effects of Lunch with Varying Glycemic Index on Children’s Cognitive Function—CogniDo GI-II
Farfel, Gail
IP 1184. ZX008 (Fenfluramine) in Dravet’s Syndrome: First Results of a Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial
Fassbender, Jessica
P 1086. Role of PTRH2 in Cerebellar Development
Fazeli, Walid
FV 992. Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech Development
FV 1165. Limb Ischemia and Arterial Ischemic Stroke in a Newborn: Coincidence or Common Cause?
P 613. IQSEC2-Associated X-Coupled Mental Retardation 1 in a Girl with Difficult-to-Treat Epilepsy
P 1001. A Pathogenic GABRB3 Variant Is Associated with Cleft Palate in a Patient with Epileptic Encephalopathy
Fiedler, Barbara
FV 837. Early Withdrawal of Antiepileptic Medication in Patients with Juvenile Myoclonic Epilepsy Is Justifiable!
FV 921. What Do Teachers Know about Epileptic Seizures or Epilepsy in School?
FV 1178. The More the Merrier? Diagnostic Yield of EEG after the First Unprovoked Seizure
FV 1177. Genetic Causes of Congenital Hydrocephalus
P 856. Andermann’s Syndrome—Symptom Complex of Agenesis of the Corpus Callosum and Motor–Sensory Neuropathy
P 967. IRIS—A Dreaded Complication of Tuberculous Meningitis
P 644. Diagnosis of Muscle–Eye–Brain Disease through Characteristic Neuroradiological Findings
Fink, Christian
P 366. 7q11.23 Microduplication Syndrome: Neurophysiological and Neuroradiological Insights into a Rare Chromosomal Disorder
Fischer, Meike
FV 969. Transplantation Surgery Used Autologous Transgenic Keratinocyte Cultures Which Regenerated an Entire, Fully Functional Epidermis
Fischer, Michal
P 1106. Involvement of the Cardial Autonomous Nervous System in Mitochondrial Neurogastrointestinal Encephalopathy Syndrome
Fluss, Joel
FV 571. Cardiac Kids with Stroke
Foust, Kevin D.
IP 853. AVXS-101 Phase-1-Gene Therapy Clinical Trial in SMA Type 1: Event-Free Survival and Achievement of Developmental Milestones
Frank, Diana
FV 1177. Genetic Causes of Congenital Hydrocephalus
Frank, Nathalie
P 1111. Case Report of a Juvenile Patient with Niemann–Pick’s Disease Type C
Freisinger, Peter
FV 754. Newborn Screening, a Disease-Modifying Intervention for Glutaric Aciduria Type 1
Frölich, Saskia
FV 300. Living with Severe Rare Chronic Neurological Disease in Childhood: Family Burden and Quality of Life in Families with MLD and PCH2
Funk, Julia
P 980. Selective Motor Control Improves after Selective Dorsal Rhizotomy
P 1175. Increased Quality of Life in Children with Cerebral Palsy after Selective Dorsal Rhizotomy
P 882. Four-Level Release (Rideau) and Glucocorticoid Therapy in Patients with DMD—Additive Positive Effect on Ambulation