No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy

Author： Madia F.   Gennaro E.   Cecconi M.   Buti D.   Capovilla G.   Dalla Bernardina B.   Elia M.   Ferrari A.   Fontana E.   Gaggero R.   Giannotta M.   Giordano L.   Granata T.   La Selva L.   Luisa Lispi M.   Santucci M.   Vanadia F.   Veggiotti P.   Vigliano P.   Viri M.   Dagna Bricarelli F.   Bianchi A.   Zara F.  

Publisher： Elsevier

ISSN： 0920-1211

Source： Epilepsy Research, Vol.53, Iss.3, 2003-03, pp. : 196-200

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Na v 1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents

By Sugawara T.   Tsurubuchi Y.   Fujiwara T.   Mazaki-Miyazaki E.   Nagata K.   Montal M.   Inoue Y.   Yamakawa K.  

Epilepsy Research, Vol. 54, Iss. 2, 2003-05 ,pp. : 201-207

Elsevier

Access to resources Recommend Favorite

Topiramate as add-on drug in severe myoclonic epilepsy in infancy: an Italian multicenter open trial

By Coppola G.   Capovilla G.   Montagnini A.   Romeo A.   Spano M.   Tortorella G.   Veggiotti P.   Viri M.   Pascotto A.  

Epilepsy Research, Vol. 49, Iss. 1, 2002-03 ,pp. : 45-48

Elsevier

Access to resources Recommend Favorite

Severe myoclonic epilepsy and mitochondrial cytopathy

By Castro-Gago M.   Eirís-Puñal J.   Martinón Sánchez J. M.   Rodríguez-Nuñez A.   Herranz Fernández J. L.  

Child's Nervous System, Vol. 13, Iss. 11-12, 1997-12 ,pp. : 570-571

Springer Publishing Company

Access to resources Recommend Favorite

Absence of mutations in major GEFS+ genes in myoclonic astatic epilepsy

By Nabbout R.   Kozlovski A.   Gennaro E.   Bahi-Buisson N.   Zara F.   Chiron C.   Bianchi A.   Brice A.   Leguern E.   Dulac O.  

Epilepsy Research, Vol. 56, Iss. 2, 2003-10 ,pp. : 127-133

Elsevier

Access to resources Recommend Favorite

Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families

By Madia Francesca  

Neurogenetics, Vol. 9, Iss. 2, 2008-05 ,pp. : 139-142

Springer Publishing Company

Access to resources Recommend Favorite