Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers.

Weckhuysen, Sarah; Holmgren, Philip; Hendrickx, Rik; Jansen, Anna C; Hasaerts, Daniele; Dielman, Charlotte; de Bellescize, Julitta; Boutry-Kryza, Nadia; Lesca, Gaetan; Von Spiczak, Sarah; Helbig, Ingo; Gill, Deepak; Yendle, Simone; Møller, Rikke S; Klitten, Laura; Korff, Christian; Godfraind, Catherine; Van Rijckevorsel, Kenou; De Jonghe, Peter; Hjalgrim, Helle; Scheffer, Ingrid E; Suls, Arvid

Weckhuysen, Sarah; Holmgren, Philip; Hendrickx, Rik; Jansen, Anna C; Hasaerts, Daniele; Dielman, Charlotte; de Bellescize, Julitta; Boutry-Kryza, Nadia; Lesca, Gaetan; Von Spiczak, Sarah; Helbig, Ingo; Gill, Deepak; Yendle, Simone; Møller, Rikke S; Klitten, Laura; Korff, Christian; Godfraind, Catherine; Van Rijckevorsel, Kenou; De Jonghe, Peter; Hjalgrim, Helle; Scheffer, Ingrid E; Suls, Arvid.

Affiliation

Weckhuysen S; Neurogenetics Group, Department of Molecular Genetics, VIB, Antwerp, Belgium.

Epilepsia ; 54(5): e74-80, 2013 May.

Article in En | MEDLINE | ID: mdl-23409955

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Seizures / Spasms, Infantile / Genetic Predisposition to Disease / Munc18 Proteins / Mutation Type of study: Etiology_studies Limits: Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Epilepsia Year: 2013 Document type: Article Affiliation country: Country of publication:

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