Yukiyoshi Shirasaka

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 · 187 citations

Life Sciences, Genetics, Molecular Genetics +17

A human Dravet syndrome model from patient induced pluripotent stem cells

Norimichi Higurashi, Taku Uchida, Christoph Lossin et al. · Molecular Brain · 2013 · 147 citations · Full text

Life Sciences, Genetics, Neuroscience +17

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

Medicine, Genetics, Molecular Genetics +17

Self‐Sustaining Status Epilepticus: A Condition Maintained by Potentiation of Glutamate Receptors and by Plastic Changes in Substance P and Other Peptide Neuromodulators

Claude G. Wasterlain, Hantao Liu, Andrey M. Mazarati et al. · Epilepsia · 2000 · 53 citations · Full text

Life Sciences, Neuroscience, Pharmacology +17

Rufinamide as an adjunctive therapy for Lennox–Gastaut syndrome: A randomized double-blind placebo-controlled trial in Japan

Yoko Ohtsuka, Harumi Yoshinaga, Yukiyoshi Shirasaka et al. · Epilepsy Research · 2014 · 53 citations · Full text

Medicine, Pharmacology, Pharmacotherapy +14