Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine
Top Cited Papers
- 1 July 2005
- journal article
- Published by Elsevier BV in The Lancet
- Vol. 366 (9483), 371-377
- https://doi.org/10.1016/s0140-6736(05)66786-4
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- Kinetic Alterations due to a Missense Mutation in the Na,K-ATPase α2 Subunit Cause Familial Hemiplegic Migraine Type 2Journal of Biological Chemistry, 2004
- Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancyPediatric Neurology, 2004
- Deciphering migraine mechanisms: Clues from familial hemiplegic migraine genotypesAnnals of Neurology, 2004
- Novel mutations in the Na+, K+‐ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsionsAnnals of Neurology, 2003
- Neurobiology of migraineNature Reviews Neuroscience, 2003
- Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23Annals of Neurology, 2003
- De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of InfancyAmerican Journal of Human Genetics, 2001
- Mapping of a second locus for familial hemiplegic migraine to 1q21–q23 and evidence of further heterogeneityAnnals of Neurology, 1997
- Structural parts involved in activation and inactivation of the sodium channelNature, 1989
- COMPOUNDS IN BRAIN EXTRACTS CAUSING SPREADING DEPRESSION OF CEREBRAL CORTICAL ACTIVITY AND CONTRACTION OF CRUSTACEAN MUSCLEJournal of Neurochemistry, 1959