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
VS13_01
Baumgartner, S; Rostásy, K; Haberlandt, E; Baumann, M: Jeavon syndrome as a differential diagnosis of facial tics
VS13_02
Heimering, S; Abicht, A; Fiedler, A: A new heterozygote sequence variant of the CDKL5 Gene as the underlying cause of intractable early infantile epilepsy
VS13_03
Wille, DA; Hackenberg, A; Rauch, A; Kröll, J; Schmitt, B; Plecko, B: Infantile choreatic movements, early onset severe epileptic encephalopathy, and primary developmental impairment as a result of a de novo missense mutation in the SCN2A gene
VS13_04
Böhringer, E; Kluger, G; Steinbeis-von Stülpnagel, C; Kohlschütter, A; Meyer-Osores, A; Hagel, C; Baethmann, M; Leiz, S: Lafora disease in a 17-year-old boy due to a compound heterozygous mutation in the NHLRC1 gene
VS13_05
Gosk, M; Laccone, F; Burfeind, P; Bernert, G: Progressive myoclonus epilepsy: a differential diagnosis from juvenile chorea Huntington disease
VS13_06
Brueckner, F; Kohl, B; Püst, B; Gassner, S; Biskup, S; Stodieck, S; Lohmann, E: Paroxysmal dyskinesia due to PRRT2 mutation in 15-year-old female patient with benign familial infantile convulsions
VS13_07
Kurlemann, G; Linden, T; Elpers, C; Fiedler, B: Listening is all important!
VS13_08
Staudt, M; Paglioli, E; Pascoal, T; Menezes, R; Palmini, A: Immediate improvement of paretic hand function after epilepsy surgery in congenital hemiparesis