Sawa Yasumoto

Mutations of Neuronal Voltage‐gated Na⁺ Channel α1 Subunit Gene <i>SCN1A</i> in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)

Goryu Fukuma, Hirokazu Oguni, Yukiyoshi Shirasaka et al. · Epilepsia · 2004 · 186 citations

Missense mutation of the sodium channel gene SCN2A causes Dravet syndrome

Xiu‐Yu Shi, Sawa Yasumoto, Eiji Nakagawa et al. · Brain and Development · 2009 · 128 citations

Channelopathies, Dravet Syndrome, Sodium Homeostasis +7

Clinical Features of Acute Flaccid Myelitis Temporally Associated With an Enterovirus D68 Outbreak: Results of a Nationwide Survey of Acute Flaccid Paralysis in Japan, August–December 2015

Pin Fee Chong, Ryutaro Kira, Harushi Mori et al. · Clinical Infectious Diseases · 2017 · 122 citations · Full text

Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan

Hiroyuki Torisu, Ryutaro Kira, Yoshito Ishizaki et al. · Brain and Development · 2009 · 109 citations

Neurological Disorder, Medicine, Pediatrics +7

Microchromosomal deletions involving <i>SCN1A</i> and adjacent genes in severe myoclonic epilepsy in infancy

Ji‐wen Wang, Hirokazu Kurahashi, Atsushi Ishii et al. · Epilepsia · 2008 · 68 citations · Full text