Hirokazu Oguni

Mutations in EFHC1 cause juvenile myoclonic epilepsy

Toshimitsu Suzuki, Antonio V. Delgado‐Escueta, Kripamoy Aguan et al. · Nature Genetics · 2004 · 373 citations

Medicine, Genetics, Molecular Genetics +12

Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group

Joerg Klepper, Cigdem I. Akman, Marisa Armeno et al. · Epilepsia Open · 2020 · 276 citations · Full text

Medicine, Neurology, Neuroscience +17

Treatment and Long-Term Prognosis of Myoclonic-Astatic Epilepsy of Early Childhood

Hirokazu Oguni, Teruyuki Tanaka, Keiko Hayashi et al. · Neuropediatrics · 2002 · 197 citations

Medicine, Neurology, Pharmacotherapy +17

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

Severe myoclonic epilepsy in infancy: Dravet syndrome.

Charlotte Dravet, Michelle Bureau, Hirokazu Oguni et al. · PubMed · 2005 · 181 citations

Medicine, Neurology, Pediatrics +14