DOI : 10.1055/s-00000041

Neuropediatrics

Ausgabe S 02 · Volume 50 · September 2019 DOI: 10.1055/s-009-44190


Abstracts of the 45th Annual Meeting of the Society for Neuropediatrics
München, 11.09 – 14.09.2019

Chair: Prof. Dr. Martin Staudt, Pediatric Neurology, Neurorehabilitation and Epileptology, Schön Klinik Vogtareuth
Abstracts (HTML) Autorenliste
GNP-PO24
Stephani, Ulrich; Nabbout, Rima; Auvin, Stéphane; Zuberi, Sameer; Villeneuve, Nathalie; Nagel, Antonio Gil; Sanchez-Carpintero, Rocio; Chiron, Catherine; Farfel, Gail; Galer, Bradley; Morrison, Glenn; Lock, Michael; Mistry, Arun; Polster, Tilman: Less Convulsive Seizures by Fenfluramin Medication in Stiripentol Treated Patients with Dravet's Syndrome: Results from Randomized, Placebo-controlled Phase 3 Clinical Trial
GNP-PO25
Pringsheim, Milka; Kluger, Gerhard; Brandl, Ulrich; Jacobs, Julia; Mayer, Thomas; Panzer, Axel; Stephani, Ulrich; Wolff, Markus; Lagae, Lieven; Nabbout, Rima; Farfel, Gail; Galer, Bradley; Morrison, Glenn; Lock, Michael; Gammaitoni, Arnold; Mist, Arun: Fenfluramine HCl (Fintepla®) Provides Long-Term Clinically Meaningful Reduction in Seizure Frequency: Results of an Open-Label Extension Study
GNP-PO26
Pringsheim, Milka; Kluger, Gerhard; Brandl, Ulrich; Jacobs, Julia; Mayer, Thomas; Panzer, Axel; Stephani, Ulrich; Wolff, Markus; Lagae, Lieven; Nabbout, Rima; Farfel, Gail; Galer, Bradley; Morrison, Glenn; Lock, Michael; Gammaitoni, Arnold: Long-term Data on the Cardiovascular Safety Profile of Fenfluramine in the Treatment of Dravet Syndrome: Interim Analysis of an Open-label Safety Extension Study
GNP-PO27
Kürsten, Marianne; Tacke, Moritz; Gerstl, Lucia; Hoelz, Hannes; von Stülpnagel, Celina Steinbeis; Borggräfe, Ingo: Treatment of KCNQ2 Related Epilepsy
GNP-PO28
Mammadova, Dilbar; Kraus, Cornelia; Leis, Thomas; Trollmann, Regina: Severe Epileptic Encephalopathy in Siblings due to a Novel Heterozygous CACNA1A Gene Mutation
GNP-PO29
Hermann, Katharina; Johannsen, Jessika; Kloth, Katja; Denecke, Jonas: Late Diagnosis of Pyridoxine-dependent Epilepsy due to a PROSC-mutation with Whole-exome-Sequencing and Natural History without Administration of Pyridoxine until Adolescence
GNP-PO30
Gasser, Marius; Boonsimma, Ponghatai; Netbaramee, Wiracha; Wechapinan, Thanin; Srichomthomg, Chalurmpon; Ittiwut, Chupong; Krenn, Martin; Zimprich, Fritz; Milenkovic, Ivan; Abicht, Angela; Biskup, Saskia; Roser, Timo; Suphapeetiporn, Kanya; Shotelersuk, Vorasuk; Tacke, Moritz; Kürsten, Marianne; Wagner, Matias; Borggräfe, Ingo; von Stülpnagel-Steibeis, Celina: ATP1A3-related Epilepsy: Report of Six Cases and Literature-based Analysis of Treatment Response
GNP-PO31
Lübbig, Anja; Kluger, Gerhard Josef; Neuhann, Teresa; Balg, Stefanie; Staudt, Martin: A SCN1A – Positive Family with Paroxysmal Events Triggered by Infection and Emotion in Childhood and Basilar-type Migraine in Adulthood
GNP-PO32
Kyoseva, Mariya; Kluger, Gerhard; Berger, Andrea; Staudt, Martin; Haberlandt, Edda; Betzler, Cornelia; Pringsheim, Milka: Difficult-to-treat Epilepsies in Children with SMC1A Mutations without Facial Abnormalities: An “Atypical Cornelia-de-Lange Syndrome“? – Five More Cases
GNP-PO33
Willimsky, Eva-Katharina; Munzig, Anna; Mayer, Karin; Abicht, Angela; Biskup, Saskia; von Voss, Hubertus; Klein, Hanns-Georg; Rost, Imma; Borggraefe, Ingo: The Impact of Panel Size in Next Generation Sequencing in Pediatric Epilepsy
GNP-PO34
Hölz, Hannes Leon; Herdl, Christian; Gerstl, Lucia; Tacke, Moritz; Vill, Katharina; von Stülpnagel, Celina; Rost, Imma; Hörtnagel, Konstanze; Abicht, Angela; Hollizeck, Sebastian; Larsen, Line H. G.; Borggräfe, Ingo: Impact on Clinical Decision Making of Next-generation Sequencing (NGS) in Pediatric Epilepsy in a Tertiary Epilepsy Referral Center