Neuropediatrics

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• Poster

• Postersession 5: Epilepsie II, Genetik

P096

Schoene-Bake, JC; Wagner, J; Elger, CE; Weber, B:

A method for automated volumetry to assess disease progression in Rasmussen Encephalitis

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P097

Ensslen, M; Blaschek, A; Heinen, F; Penzien, J; Borggräfe, I:

Anti-NMDAR Encephalitis in children: Delineation of the epileptic phenotypes

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P098

Hannibal, I; Huß, K; Grossmann, R; Heinen, F; Borggräfe, I:

DYT 11 Myoclonus-Dystonia Syndrome (MDS) with generalized epileptic discharges

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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

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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

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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

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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

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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

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P104

Ries, M; Moog, U; Karch, S; Seitz, A; Kohlhase, J; Pietz, J; Wolf, NI:

Syndactyly, tremor, and hypomyelination associated with oculodentodigital dysplasia

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P105

Koy, A; Klee, D; Weber, AA; Karenfort, M; Mayatepek, E:

Crossed cerebellar diaschisis after status epilepticus

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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

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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?

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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

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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

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P110

Poretti, A; Huisman, TAGM; Scheer, I; Boltshauser, E:

Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients

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P111

Fiedler, BJ; Siebers-Renelt, U; Bohring, A; Schwindt, W; Kurlemann, G:

Potocki-Shaffer Syndrome: A case study

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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

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P113

Weiss, D; Walsh, S; Haffner, D; Denecke, J:

Familial occurence of congenital bilateral perisylvian syndrom

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P114

Walsh, S; Weiss, D; Kirchhoff, F; Haffner, D; Denecke, J:

Kleine-Levin syndrome: a disorder with recurring hypersomnia as main symptom

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P115

Rosenbaum, T; Kennerknecht, I; Plümpe, N:

Hereditary prosopagnosia

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P116

Berger, A; Kutschke, G; Crow, YJ; Reitter, B:

A case of familial Labrune syndrome

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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

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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

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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

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P120

Kovacevic-Preradovic, T; Mayer, T; Holert, N:

Isolated corpus callosum agenesis as a rare differenzial diagnosis of attention defficit hyperactivity disorder- case report

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