Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations.

Milh, Mathieu; Villeneuve, Nathalie; Chouchane, Mondher; Kaminska, Anna; Laroche, Cécile; Barthez, Marie Anne; Gitiaux, Cyril; Bartoli, Céline; Borges-Correia, Ana; Cacciagli, Pierre; Mignon-Ravix, Cécile; Cuberos, Hélène; Chabrol, Brigitte; Villard, Laurent

Milh, Mathieu; Villeneuve, Nathalie; Chouchane, Mondher; Kaminska, Anna; Laroche, Cécile; Barthez, Marie Anne; Gitiaux, Cyril; Bartoli, Céline; Borges-Correia, Ana; Cacciagli, Pierre; Mignon-Ravix, Cécile; Cuberos, Hélène; Chabrol, Brigitte; Villard, Laurent.

Affiliation

Milh M; APHM, CINAPSE, Pediatric Neurology Department, Timone Children Hospital, Marseille, France. mathieu.milh@ap-hm.fr

Epilepsia ; 52(10): 1828-34, 2011 Oct.

Article in En | MEDLINE | ID: mdl-21770924

Subject(s)

Epilepsy/genetics; Munc18 Proteins/genetics; Age of Onset; Anticonvulsants/therapeutic use; Brain/pathology; Brain/physiopathology; Electroencephalography; Epilepsy/drug therapy; Epilepsy/pathology; Epilepsy/physiopathology; Genotype; Humans; Infant; Infant, Newborn; Magnetic Resonance Imaging; Mutation; Oligonucleotide Array Sequence Analysis; Syndrome; Video Recording

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy / Munc18 Proteins Type of study: Clinical_trials Limits: Humans / Infant / Newborn Language: En Journal: Epilepsia Year: 2011 Type: Article Affiliation country: France

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