Ion channel gene defects

Citations 91-93 of 93 total displayed.

Past content (since Aug 2001):

BRIEF COMMUNICATIONS
Pathogenic effect of an intermediate-size SCA-6 allele (CAG)₁₉ in a homozygous patient

C. Mariotti, C. Gellera, M. Grisoli, R. Mineri, A. Castucci, and S. Di Donato
Neurology 2001; 57: 1502-1504. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Sodium channel gene mutations in hypokalemic periodic paralysis: An uncommon cause in the UK

N. P. Davies, L. H. Eunson, M. Samuel, and M. G. Hanna
Neurology 2001; 57: 1323-1325. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Na_v1.1 mutations cause febrile seizures associated with afebrile partial seizures

T. Sugawara, E. Mazaki–Miyazaki, M. Ito, H. Nagafuji, G. Fukuma, A. Mitsudome, K. Wada, S. Kaneko, S. Hirose, and K. Yamakawa
Neurology 2001; 57: 703-705. [Abstract] [Full text] [PDF]  

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