DOI : 10.1055/s-00000041

Neuropediatrics

Issue 02 · Volume 44 · March 2013 DOI: 10.1055/s-003-24657


Abstracts of the 39th Annual Meeting of the Society of Neuropediatrics
Innsbruck, 25th to 28th April 2013

Chair: PD Dr. Kevin Rostásy, Kinderklinik Innsbruck, Medizinische Universität Innsbruck
Abstracts (HTML) List of Authors
PS19_1166
Reihle, C; Kalle, T von; Severien, C; Marquard, K; Biskup, S; Blankenburg, M: Biotin-responsive basal ganglia disease in a 10-year-old German girl without SLC19A3 gene mutation
PS19_1258
Elpers, C; Fiedler, B; Schwartz, O; Linden, T; Omran, H; Kurlemann, G: Ketogenic diet in children with pharmacoresistant epilepsy
PS19_1229
Schober, H; Konzett, K; Lütschg, J; Paschke, E; Plecko, B; Simma, B: Pyridoxine-dependent epilepsy: case report
PS19_1216
Koch, J; Mayr, JA; Scheffner, T; Makowski, C; Zimmermann, F; Maier, E; Debus, O; Marquardt, T; Schlachter, K; Schneider, HC; Prokisch, H; Sperl, W; Freisinger, P: Clinical symptoms of six children with thiamin pyrophosphokinase deficiency
PS19_1276
Maier, E; Koch, J; Mayr, J; Rauscher, C; Maxonus, I; Freilinger, M; Wagentristl, HP; Sperl, W: Atypical and mild clinical manifestation in a boy with mitochondrial ATP6 mutation
PS19_1204
Weigt-Usinger, K; Thiels, C; Köhler, C; Heyer, C; Hinderhofer, K; Assmann, B; Opladen, T; Lücke, T: Choreatic movement disorder due to tyrosine hydroxylase deficiency caused by a novel mutation in the TH gene
PS19_1226
Schulz, A: DEM-CHILD – a treatment-oriented research project of NCL disorders as a major cause of dementia in childhood
PS19_1196
Thiels, C; Weigt-Usinger, K; Kölker, S; Janzen, N; Baumgartner, M; Köhler, C; Lücke, T: Methylenetetrahydrofolate reductase deficiency: therapy and outcome (with video)
PS19_1262
Fiedler, B; Bimböse, P; Omran, H; Kurlemann, G: Vitamin B in paediatric neurology
PS19_1041
Giagkou, E; Lutz, S; Schara, U; Becker, K; Möller-Hartmann, C: Neurodegeneration with brain iron accumulation type 4 by mutation in the C19orf12 gene: first time found in adolescent of Russian origin