DOI : 10.1055/s-00000041

Neuropediatrics

Issue 02 · Volume 43 · April 2012 DOI: 10.1055/s-002-23054


Abstracts of the 38th Annual Meeting of the Society of Neuropediatrics
Münster, 19th to 22nd April 2012

Chair: Prof. Dr. med. Gerhard Kurlemann, Münster
Abstracts (HTML) List of Authors
PS18_01
Sarrazin, E; der Hagen, M von; Schara, U; Au, K von; Kaindl, A: Growth and psychomotor development of patients with Duchenne Muscular Dystrophy
PS18_02
Trippe, H; Munteanu, M; Lutz, S; Schara, U: Mutation in the Fukutin-Gene (FKTN) as cause of a mild congenital muscular dystrophy
PS18_04
Beytia, M; Vry, J; Kirschner, J: Manifestation of muscular dystrophy by Anoctamin-5 mutation in infancy
PS18_05
Freudenberg, L; Stenzel, W; Laass, M; Pargac, K; Hahn, G; Knöfler, R; Goebel, H; Mall, V; Smitka, M; der Hagen, M von: Unusual presentation of juvenile Pompe disease in infancy with preceding immune thrombocytopenia
PS18_06
Blaschek, A; Strobl-Wildemann, G; Kreß, W; Heinen, F; Müller-Felber, W: Familial mutation in ACTA1 gene – clinical variability
PS18_07
Lutz, S; Buyse, G; Meier, T; Schara, U: DELOS Phase III Study with Idebenone (Catena®) in Duchenne Muscular Dystrophy
PS18_09
Herzog, A; Hartung, R; Karabul, N; Beck, M; Mengel, E: Respiration and its correlation with motoric function in non-classic Pompe disease
PS18_10
Vieker, S; Zinck, D; Längler, A; Wortmann, S: First discription of a Kearns-Sayre-like-syndrome with ragged red fibres and cerebral folate deficiency
PS18_11
Böhringer, E; Weber, P: Isolated neonatal bilateral palsy of the n. radialis; case report and review of the literature
PS18_12
Classen, G; Münter, S; Middelhoff, C; Böhm, R; Otte, J: Symptomatic Treatment of Tomaculous Polyneuropathy with Methylprednisolone
PS18_13
Kehrer, C; Gröschel, S; Müller, I; Krägeloh-Mann, I: Stem cell transplantation (SCT) in metachromatic leukodystrophy (MLD) – results from 9 patients