GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction-Reference-Cited by-同舟云学术

GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction

Published:2013-08-11 Issue:9 Volume:45 Page:1061-1066
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Lesca Gaetan,Rudolf Gabrielle,Bruneau Nadine,Lozovaya Natalia,Labalme Audrey,Boutry-Kryza Nadia,Salmi Manal,Tsintsadze Timur,Addis Laura,Motte Jacques,Wright Sukhvir,Tsintsadze Vera,Michel Anne,Doummar Diane,Lascelles Karine,Strug Lisa,Waters Patrick,de Bellescize Julitta,Vrielynck Pascal,de Saint Martin Anne,Ville Dorothee,Ryvlin Philippe,Arzimanoglou Alexis,Hirsch Edouard,Vincent Angela,Pal Deb,Burnashev Nail,Sanlaville Damien,Szepetowski Pierre

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2726.pdf

Reference36 articles.

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3. Patry, G., Lyagoubi, S. & Tassinari, C.A. Subclinical “electrical status epilepticus” induced by sleep in children. A clinical and electroencephalographic study of six cases. Arch. Neurol. 24, 242–252 (1971).

4. Nieuwenhuis, L. & Nicolai, J. The pathophysiological mechanisms of cognitive and behavioral disturbances in children with Landau-Kleffner syndrome or epilepsy with continuous spike-and-waves during slow-wave sleep. Seizure 15, 249–258 (2006).

5. Van Bogaert, P. & Paquier, P.F. Landau-Kleffner syndrome: 50 years after. Epilepsia 50 (suppl. 7), 1–2 (2009).

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