相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Two novel SCNIA mutations identified in families with familial hemiplegic migraine
Claudia M. Weller et al.
CEPHALALGIA (2014)
Pearls and pitfalls in genetic studies of migraine
Else Eising et al.
CEPHALALGIA (2013)
PRRT2 mutations and paroxysmal disorders
A. Meneret et al.
EUROPEAN JOURNAL OF NEUROLOGY (2013)
Genome-wide meta-analysis identifies new susceptibility loci for migraine
Verneri Anttila et al.
NATURE GENETICS (2013)
How should we be searching for genes for common epilepsy? A critique and a prescription
David A. Greenberg et al.
EPILEPSIA (2012)
PRRT2 mutations cause hemiplegic migraine
Florence Riant et al.
NEUROLOGY (2012)
A Simple Method for Analyzing Exome Sequencing Data Shows Distinct Levels of Nonsynonymous Variation for Human Immune and Nervous System Genes
Jan Freudenberg et al.
PLOS ONE (2012)
A long-term follow-up study of 18 patients with sporadic hemiplegic migraine
Anine H. Stam et al.
CEPHALALGIA (2011)
Sporadic and familial hemiplegic migraine: pathophysiological mechanisms, clinical characteristics, diagnosis, and management
Michael Bjorn Russell et al.
LANCET NEUROLOGY (2011)
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine
F. Riant et al.
NEUROLOGY (2010)
First mutation in the voltage-gated NaV1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy
M-J Castro et al.
CEPHALALGIA (2009)
Molecular genetics of migraine
Boukje de Vries et al.
HUMAN GENETICS (2009)
Elicited repetitive daily blindness A new phenotype associated with hemiplegic migraine and SCN1A mutations
K. Vahedi et al.
NEUROLOGY (2009)
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine
M Dichgans et al.
LANCET (2005)
Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2
M De Fusco et al.
NATURE GENETICS (2003)
分享论文
