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Epilepsy Research|February 2, 2002

Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1AM Ito, H Nagafuji, H Okazawa, et al.

Neurology|July 28, 2004

Effect of localization of missense mutations in SCN1A on epilepsy phenotype severityK Kanai, S Hirose, H Oguni, et al.

Annals of Neurology|June 14, 2000

A novel mutation of KCNQ3 (c.925T-->C) in a Japanese family with benign familial neonatal convulsionsS Hirose, F Zenri, H Akiyoshi, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 24, 2001

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunctionT Sugawara, Y Tsurubuchi, K L Agarwala, et al.

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Showing results (41-50 of 44) with videos related to

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You have reached the last page of results.This site can display upto 44 results.

Epilepsy Research|February 2, 2002

Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1AM Ito, H Nagafuji, H Okazawa, et al.

Neurology|July 28, 2004

Effect of localization of missense mutations in SCN1A on epilepsy phenotype severityK Kanai, S Hirose, H Oguni, et al.

Annals of Neurology|June 14, 2000

A novel mutation of KCNQ3 (c.925T-->C) in a Japanese family with benign familial neonatal convulsionsS Hirose, F Zenri, H Akiyoshi, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 24, 2001

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunctionT Sugawara, Y Tsurubuchi, K L Agarwala, et al.

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