DOI : 10.1055/s-00000041

Neuropediatrics

Issue S 01 · Volume 46 · April 2015 DOI: 10.1055/s-005-28977


Abstracts of the 41st Annual Meeting of the Society of Neuropediatrics
Basel, 23–26 April 2015

Prof. Dr. Peter Weber

  • PS02-01
    Heußinger, N.; Kontopantelis, E.; Gburek-Augustat, J.; Jenke, A.; Vollrath, G.; Korinthenberg, R.; Hofstetter, P.; Meyer, S.; Brecht, I.; Bajer-Kornek, B.; Herkenrath, P.; Schimmel, M.; Wenner, K.; Häusler, M.; Lutz, S.; Blaschek, A.; Smitka, M.; Karch, S.; Piepkorn, M.; Rostasy, K.; Weber, P.; Trollmann, R.; Klepper, J.; Häußler, M.; Hofmann, R.; Weissert, R.; Merkenschlager, A.; Buttmann, M.:

    Oligoclonal Bands Predict Multiple Sclerosis in Children with Isolated Optic Neuritis: A Retrospective Multicenter Cohort Study

  • PS02-03
    Zielonka, M.; Assmann, B.; Sommerburg, O.; Hoffmann, G.; Junghanss, T.; Ziegler, A.:

    Diagnostic Pitfalls in Tuberculous Meningitis

  • PS02-04
  • PS02-05
    Idris, N.; Cagnoli, S.; Jenke, A.; Borusiak, P.:

    EBV Encephalitis in Acute Infectious Mononucleosis

  • PS02-06
    Damm, M.; Wörle, H.; Reihle, C.; von Kalle, T.; Blankenburg, M.:

    MERS: Mild Encephalopathy/Encephalitis with Reversible Lesions in the Splenium Another Three Cases

  • PS02-07
    Reihle, C.; von Kalle, T.; Schmiedel, G.; Severin, C.; Sauter, T.; Marquard, K.; Blankenburg, M.:

    Longitudinally Extensive Transverse Myelitis in Four Children

  • PS02-08
    Rehm, D.; Schneider, J.; Heininger, U.; André, M.; Tacke, U.:

    Acute Hemiparesis Revealing Neuroborreliosis in a 3-Year-Old Boy

  • PS02-09
    Elpers, C.; Groß, C.; Althaus, J.; Fiedler, B.; Meuth, S.; Kurlemann, G.:

    Predictive Value of Cerebrospinal Fluid Flow Cytometry in Pediatric Multiple Sclerosis

  • PS02-10
  • PS02-11
    Jünemann, S.; Steiner, B.; Röthlisberger, B.; Schmitt-Mechelke, T.:

    Old Drug, New Mutation in Neonatal Epileptic Encephalopathies

  • PS02-12
    Herbst, S.; Geis, T.; Borggräfe, I.; Debus, O.; Häußler, M.; Phillipi, H.; Ross, S.; Vosschulte, P.; Rossegg, U.; Beaud, N.; Budde, J.; Hahn, A.; Kurlemann, G.; Hehr, U.:

    Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly

  • PS02-14
    Jelesch, E.; Eitel, H.; Betzler, C.; Pringsheim, M.; Herberhold, T.; Pieper, T.; Till, H.; Winkler, P.; Biskup, S.; Hörtnagel, K.; Staudt, M.; Kluger, G.:

    Focal Cortical Dysplasia in a Family with KCNQ3 Mutation

  • PS02-15
    Neumann, H.; Weigt-Usinger, K.; Selzer, L.; Helmke, F.; Thiels, C.; Daseking, M.; Petermann, F.; Lücke, T.:

    Cognitive Development in Children with Rolandic Epilepsy: Results of a Current PubMed Search

  • PS02-16
    Koehler, K.; Münter, S.; Hamelmann, E.; Classen, G.:

    Case Report of a Patient with partial Trisomy 13q21.1qter

  • PS02-17
  • PS02-18
    Selzer, L.; Weigt-Usinger, K.; Neumann, H.; Helmke, F.; Thiels, C.; Köhler, C.; Lücke, T.:

    Rolandic Epilepsy: Retrospective Analysis of Neuropsychological and Clinical Data

  • PS02-19
  • PS02-20
    Lotte, J.; Bast, T.; Borusiak, P.; Coppola, A.; Cross, H.; Dimova, P.; Fogarasi, A.; Graness, I.; Guerrini, R.; Hjalgrim, H.; Kurlemann, G.; Leiz, S.; Linder-Lucht, M.; Loddenkemper, T.; Makowski, C.; Mühe, C.; Müller, A.; Nicolai, J.; Pellacani, S.; Philip, S.; Ruf, S.; Sánchez, I. Fernández; Schlachter, K.; Striano, P.; Sukhudyan, B.; Vermeulen, J.; Wilken, B.; Wolf, P.; Kluger, G.; Weisbrod, T.; Keimer, R.:

    Therapy and Clinical Course in 52 Patients with PCDH19 Mutations

  • PS02-21
    Hubacher, M.; Oser, N.; Penner, I.; Schneider, J.; Weber, P.; Datta, A.:

    Internetwork Connectivity Alterations in Children with Benign Epilepsy with Centrotemporal Spikes

  • PS02-22
  • PS02-23
    Perret-Hoigné, E.; Steinlin, M.; Grunt, S.:

    LPIN1 Mutations are an Important Cause of Rhabdomyolysis

  • PS02-24
  • PS02-25
  • PS02-26
    Trippe, H.; Bouikidis, A.; Lutz, S.; Della Marina, A.; Hauffa, B.; Schara, U.:

    Growth and Endocrinological Evaluation in Autosomal Recessive Proximal Spinal Muscular Atrophies Type I–III

  • PS02-27
    Konzett, K.; Schober, H.; Blassnig-Ezeh, A.; Lütschg, J.; Simma, B.:

    Spinal Cord Monitoring in Patients with SMA Type III: A Case Report

  • PS02-28
    Schwerin-Nagel, A.; Brunner-Krainz, M.; Gruber-Sedlmayr, U.; Seifert-Held, T.; Stroedter, L.; Quasthoff, S.:

    Neuralgic Amyotrophy: A Rare Disease in Adolescence

  • PS02-29
  • PS02-30
  • PS02-31
  • PS02-33
    Greulich, N.; Klepper, J.; Müller, C.; Korinthenberg, R.; Heußinger, N.:

    Becker Muscular Dystrophy in a 2-Year-Old Boy caused by a Novel Missense Mutation p.Arg145Pro in the Dystrophin Gene

  • PS02-34
    Bonati, U.; Hafner, P.; Erne, B.; Thomas, E.; Rutz, E.; Frank, S.; Hilker, C.; Deuster, S.; Gloor, M.; Bieri, O.; Sinnreich, M.; Fischmann, A.; Fischer, D.:

    Improved Muscle Function in Duchenne Muscular Dystrophy using a Combination of L-Arginine and Metformin