Neuropediatrics

Issue 05 · Volume 39 · December 2008 DOI: 10.1055/s-002-16101

Abstracts of the 35th Annual Meeting of the Society of Neuropediatrics
Graz, 23.–26. April 2009

Chairman: Univ. Prof. Dr. Barbara Plecko, Graz

Abstracts (HTML) List of Authors

Free Communications: 5: Neurogenetics and varia

V38

Kohlschmidt, N.; Gross, C. D.; Kuczaty, S.; Sassen, R.; Kunz, W.: Mutation analysis of the SCN1A gene for suspected Dravet syndrome/GEFS+ – High detection yield, unsatisfactory prognostic value

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V39

Kolzter, K.; Waltz, S.; Lotte, J.; Kluger, G.: Patients with Dravet's syndrome and SCN1A-mutation with a benign course of illness – A case report with 6 patients

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V40

Stoltenburg-Didinger, G.; Martelli, M.; Zwirner, A.; Kaindl, A. M.: Neuropathologic findings in patients with primary autosomal recessive microcephaly

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V41

Schaadt, A. K.; Hasmann, S.; Hampel, O.; Hasmann, R.; Petermann, F.; Holl, R.: Evaluation of Stepping Stones Triple P – 3-year-interims-analysis of the Stepping-Stones-SPC-Multicenter-Study

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V42

Blankenburg, M.; Boekens, H.; Aksu, F.; Maier, C.; Hechler, T.; Zernikow, B.: Quantitative Sensory Testing (QST) in children and adolescents

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