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Panzer, Axel
P 256. Use of Ketogenic Diets in patients with Epilepsy and Metabolic Disorders in Germany, Austria, and Switzerland
IP 1184. ZX008 (Fenfluramine) in Dravet’s Syndrome: First Results of a Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial
Pargac, Kai-Nils
P 518. Vitamin B6-Dependent West’s Syndrome: An Unexplained Case
Pauls, Amande
FV 747. Early-Onset Progressive Dystonia in Childhood with New Mutations in KMT2B
Pechmann, Astrid
FV 880. Disorders of Coagulation in Duchenne Muscular Dystrophy?—Results of a Registry-Based Online Questionnaire
FV 953. Parents’ Experiences during the Compassionate Use Program (Nusinersen) for Patients with Spinal Muscular Atrophy Type 1—A Qualitative Interview Study
P 898. SMArtCARE: Longitudinal Data Collection of Patients with Spinal Muscular Atrophy in German-Speaking Countries
P 900. Decision Making Regarding Ventilator Support in Children with SMA type 1—A Cross-sectional Survey among German Physicians
Penning, Jeff
P 856. Andermann’s Syndrome—Symptom Complex of Agenesis of the Corpus Callosum and Motor–Sensory Neuropathy
P 644. Diagnosis of Muscle–Eye–Brain Disease through Characteristic Neuroradiological Findings
Peraud, Aurelia
FV 396. Childhood Hemorrhagic Stroke—A 7-Year Single-Center Experience
Perez, Marie-Hélène
FV 571. Cardiac Kids with Stroke
Pergande, Matthias
P 1001. A Pathogenic GABRB3 Variant Is Associated with Cleft Palate in a Patient with Epileptic Encephalopathy
Persits, Sergey
P 1171. Cervical Decompression due to Progressive Cervical Myelopathy in Children after Shunt Treatment of Neonatal E. coli Meningitis
Peterli, Judith
FV 183. Comparison of the Early Auditory Evoked Potentials during the First Month of Life in Term and Preterm Children
Petermann, Franz
P 1032. Cognitive Development in Children with Rolandic Epilepsy or Rolandic EEG Pattern—Preliminary Results of a Prospective Follow-up Study
Pfammatter, Jean-Pierre
FV 571. Cardiac Kids with Stroke
Pfister, Stefan
P 1162. Somatic Mosaics in Epileptogenic Tissue—Background and Therapeutic Implications of Molecular Changes in Structural Epilepsies
Pfurtscheller, Klaus
P 788. MOG-Ab Positive Acute Disseminated Encephalomyelitis with Asymmetric Lesions in Basal Ganglia and in Thalami
Picker-Minh, Sylvie
P 1086. Role of PTRH2 in Cerebellar Development
Plecko, Barbara
P 788. MOG-Ab Positive Acute Disseminated Encephalomyelitis with Asymmetric Lesions in Basal Ganglia and in Thalami
Plecko-Startinig, Barbara
FV 735. UBTF-Related Dementia and Parkinsonism—Case Report of a Novel Disease Entity
P 1030. MRI Pattern in Neurodegeneration with Brain Iron Accumulation and Fucosidosis Appear Similar
Poggenburg, Imke
P 256. Use of Ketogenic Diets in patients with Epilepsy and Metabolic Disorders in Germany, Austria, and Switzerland
Polster, Tilman
P 556. Ketogenic Dietary Therapies—Retrospective Assessment of 143 Children Treated at the Bethel Epilepsy Center from 2003 to 2016
IP 1184. ZX008 (Fenfluramine) in Dravet’s Syndrome: First Results of a Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial
Porto, Luciana
P 1092. The Challenging Nature of Cerebral TBC Manifestations in Children and Young Adults
Posingies, Ralph
FV 921. What Do Teachers Know about Epileptic Seizures or Epilepsy in School?
Potratz, Cornelia
P 451. Clinical Presentation of Children and Adolescents with Neurofibromatosis Type I
Pozza, Robert Dalla
FV 330. Have We Done Wrong? Long-Term Follow-up of Cardiovascular Risk Factors in Glut1-Deficiency Treated with Ketogenic Diet Therapies
Prager, Christine
FV 757. Clinical, Radiological and Genetic Spectrum of a Large Pediatric Cohort with Epilepsy
P 1098. Intravenous Nimodipine Ameliorating an Episode of Sporadic Hemiplegic Migraine with Prolonged Hemiplegia and Severe Disturbances of Cognition
Pretzel, Pablo
FV 930. Reduced Structural Connectivity in Nonmotor Networks in Children Born Preterm
Pringsheim, Milka
IP 1184. ZX008 (Fenfluramine) in Dravet’s Syndrome: First Results of a Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial
Prior, Thomas W.
IP 853. AVXS-101 Phase-1-Gene Therapy Clinical Trial in SMA Type 1: Event-Free Survival and Achievement of Developmental Milestones
Privitera, Michael
IP 112. Cannabidiol Treatment Effect and Adverse Events in Patients with Lennox–Gastaut’s syndrome: Pooled Results from Two Trials
Prokisch, Holger
FV 697. Biallelic Mutations in SCYL1 Cause CALFAN-Syndrome (Cholestasis, Acute Liver Failure, and Neurodegeneration), A Congenital Disorder of Intracellular Trafficking with a Variable Neurological Phenotype
P 605. Epileptic Encephalopathy Caused by Mitochondrial MPC-1 Deficiency Can Benefit from Ketogenic Diet—Significance of Early Genetic Testing for a Targeted Therapy
Promnitz, Gabriel
P 773. Standard Values for Cranial Magnetic Resonance Imaging in the First Year of Life