Ryutaro Kira

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

Altered white matter fractional anisotropy and social impairment in children with autism spectrum disorder

Madoka Noriuchi, Yoshiaki Kikuchi, Takashi Yoshiura et al. · Brain Research · 2010 · 181 citations

Neurodevelopmental Disorders, Psychiatry, Developmental Cognitive Neuroscience +11

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

Genotype–phenotype correlations in alternating hemiplegia of childhood

Masayuki Sasaki, Atsushi Ishii, Yoshiaki Saito et al. · Neurology · 2014 · 118 citations

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