DOI : 10.1055/s-00000041

Neuropediatrics

Ausgabe S 01 · Volume 42 · März 2011 DOI: 10.1055/s-002-21774


Abstracts of the 37th Annual Meeting of the Society of Neuropediatrics
Garmisch-Partenkirchen, 7.–10. April 2011

Prof. Dr. med. Florian Heinen, München
Abstracts (HTML) Autorenliste
P096
Schoene-Bake, JC; Wagner, J; Elger, CE; Weber, B: A method for automated volumetry to assess disease progression in Rasmussen Encephalitis
P097
Ensslen, M; Blaschek, A; Heinen, F; Penzien, J; Borggräfe, I: Anti-NMDAR Encephalitis in children: Delineation of the epileptic phenotypes
P098
Hannibal, I; Huß, K; Grossmann, R; Heinen, F; Borggräfe, I: DYT 11 Myoclonus-Dystonia Syndrome (MDS) with generalized epileptic discharges
P099
Aktas, M; Honnef, D; Häusler, M: MRI signal changes of the brain stem in children with infantile spasms are not a side effect of vigabatrin therapy
P100
Pascher, B; Pieper, T; Kessler-Uberti, S; Eitel, H; Getzinger, T; Hartlieb, T; Staudt, M; Bluemcke, I; Kudernatsch, M; Winkler, PA; Kolodziejczyk, D; Holthausen, H: "Everything but motor (EBM)" – subtotal hemispherectomy sparing the primary sensori-motor region in children with hemispheric epilepsies but without hemiparesis
P101
Keßler-Uberti, S; Pieper, T; Eitel, H; Pascher, B; Hartlieb, T; Getzinger, T; Karlmeier, A; Kudernatsch, M; Winkler, PA; Kolodziejczyk, D; Blümcke, I; Staudt, M; Holthausen, H: 12 years of pediatric epilepsy surgery – The Vogtareuth experience
P102
Hartlieb, T; Pieper, T; Kessler-Uberti, S; Eitel, HC; Getzinger, T; Pascher, B; Blümcke, I; Kudernatsch, M; Winkler, PA; Staudt, M; Holthausen, H: Presurgical evaluation and postoperative seizure-outcome in children and adolescents with intracranial tumors and drug resistant focal epilepsy
P103
Getzinger, T; Pieper, T; Keßler-Uberti, S; Pascher, B; Eitel, H; Hartlieb, T; Blümcke, I; Winkler, PA; Kudernatsch, M; Delalande, O; Staudt, M; Holthausen, H: Corpus callosotomy for children suffering from intractable focal epilepsy presenting a non-laterialized EEG and unilateral lesion
P104
Ries, M; Moog, U; Karch, S; Seitz, A; Kohlhase, J; Pietz, J; Wolf, NI: Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia
P105
Koy, A; Klee, D; Weber, AA; Karenfort, M; Mayatepek, E: Crossed cerebellar diaschisis after status epilepticus
P106
Mainberger, F; Jung, N; Zenker, M; Delvendahl, I; Wahlländer-Danek, U; Freudenberg, L; Brandt, A; Berweck, S; Winkler, T; Straube, A; Heinen, F; Mall, V: A four day course of Lovastatin improves synaptic plasticity in patients with NF-1
P107
Roloff-Messing, V; Finetti, C; Feldkamp, A; Utz, N; Rosenbaum, T: Complete occlusion of the left internal carotid artery in neurofibromatosis type 1. Congenital dysplasia or progressive occlusion?
P108
Mettin, RR; Syrbe, S; Bernhard, MK; Elix, H; Hirsch, W; Kiess, W; Merkenschlager, A: Analysis of clinical manifestations in 20 children and adolescents with tuberous sclerosis complex
P109
Syrbe, S; Bernhard, MK; Tegetmeyer, H; Schuster, V; Trantakis, C; Hirsch, W; Merkenschlager, A: Acetazolamide – an almost forgotten therapeutical option in tuberculous communicating hydrocephalus
P110
Poretti, A; Huisman, TAGM; Scheer, I; Boltshauser, E: Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients
P111
Fiedler, BJ; Siebers-Renelt, U; Bohring, A; Schwindt, W; Kurlemann, G: Potocki-Shaffer Syndrome: A case study
P112
Karch, S; Dikow, N; Koch, K; Moog, U; Pietz, J: Cohen syndrome – an important differenzial diagnosis for children with mental retardation and secondary microcephaly
P113
Weiss, D; Walsh, S; Haffner, D; Denecke, J: Familial occurence of congenital bilateral perisylvian syndrom
P114
Walsh, S; Weiss, D; Kirchhoff, F; Haffner, D; Denecke, J: Kleine-Levin syndrome: a disorder with recurring hypersomnia as main symptom
P115
Rosenbaum, T; Kennerknecht, I; Plümpe, N: Hereditary prosopagnosia
P116
Berger, A; Kutschke, G; Crow, YJ; Reitter, B: A case of familial Labrune syndrome
P117
Siegel, C; Prothmann, A; Hempel, M; Rivera-Brugués, N; Oexle, K; Makowski, C; Burdach, S: Microdeletion 1q42.12q42.2 in a boy with hypogenesis of the corpus callosum
P118
Schönfelder, J; Brocke, K; Winkler, U; Flössel, U; Geiger, K; der Hagen, M von; de Lonlay, P; Hübner, A; Smitka, M: A case of sudden cardiac death in a patient with LPIN1 gene mutation
P119
Schwerin-Nagel, A; Rötzer, K; Kroisl, P; Wagner, K; Plecko, B: Microdeletion 10q26-syndrome – A rare cause for developmental retardation, strabismus and hypoplasia of cerebellum – A case report
P120
Kovacevic-Preradovic, T; Mayer, T; Holert, N: Isolated corpus callosum agenesis as a rare differenzial diagnosis of attention defficit hyperactivity disorder- case report