Satoshi Maniwa

A Screening test for the prediction of Dravet syndrome before one year of age

Junri Hattori, Mamoru Ouchida, Junko Ono et al. · Epilepsia · 2007 · 105 citations · Full text

Life Sciences, Genetics, Pediatrics +16

Is phenotype difference in severe myoclonic epilepsy in infancy related to SCN1A mutations?

Iori Ohmori, Yoko Ohtsuka, Mamoru Ouchida et al. · Brain and Development · 2003 · 44 citations

Medicine, Genetics, Neuroscience +14

Severe Myoclonic Epilepsy in Infancy: A Long‐Term Follow‐Up Study

Yoko Ohtsuka, Satoshi Maniwa, Tatsuya Ogino et al. · Psychiatry and Clinical Neurosciences · 1991 · 24 citations

Medicine, Neurology, Pediatrics +14

Myoclonic seizures combined with partial seizures and probable pathophysiology of secondary bilateral synchrony

Katsuhiro Kobayashi, Satoshi Maniwa, Tatsuya Ogino et al. · Clinical Neurophysiology · 2000 · 14 citations

Medicine, Neurology, Neuroscience +13

Incidence of infantile spinal muscular atrophy on Shikoku Island of Japan

Kentaro Okamoto, Mitsumasa Fukuda, Isao Saito et al. · Brain and Development · 2018 · 12 citations

Medicine, Neurology, Neuromuscular Disorders +5