Perampanel in 12 patients with Unverricht-Lundborg disease
Author:
Affiliation:
1. Epilepsy Unit; Hôpital Gui de Chauliac; Montpellier France
2. Research Unit (URCMA: Unité de Recherche sur les Comportements et Mouvements Anormaux); INSERM, U661; Montpellier France
3. Centre Saint Paul-H. Gastaut; Marseille France
Funder
French League Against Epilepsy
Janssen-Cilag Company
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.13662/fullpdf
Reference14 articles.
1. Neuropsychological findings in patients with Unverricht-Lundborg disease;Ferlazzo;Epilepsy Behav,2009
2. Unverricht-Lundborg disease, a condition with self-limited progression: long-term follow-up of 20 patients;Magaudda;Epilepsia,2006
3. Localization of a gene for progressive myoclonus epilepsy to chromosome 21q22;Lehesjoki;Proc Natl Acad Sci U S A,1991
4. A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy;Muona;Nat Genet,2015
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