Haginoya, Kazuhiro

Clinical spectrum of SCN2A mutations expanding to Ohtahara syndrome

Nakamura, K., Kato, M., Osaka, H., Yamashita, S., Nakagawa, E., Haginoya, K., Tohyama, J., Okuda, M., Wada, T., Shimakawa, S., et al. (2013) · Neurology

Epilepsy research and treatmentIon channel regulation and function

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The molecular and phenotypic spectrum of IQSEC 2‐related epilepsy

Zerem, A., Haginoya, K., Lev, D., Blumkin, L., Kivity, S., Linder, I., Shoubridge, C., Palmer, E. E., Field, M., Boyle, J., et al. (2016) · Epilepsia

Epilepsy research and treatmentGenetics and Neurodevelopmental Disorders

Cited by 59

RBPJ is disrupted in a case of proximal 4p deletion syndrome with epilepsy

Nakayama, T., Saitsu, H., Endo, W., Kikuchi, A., Uematsu, M., Haginoya, K., Hino-fukuyo, N., Kobayashi, T., Iwasaki, M., Tominaga, T., et al. (2014) · Brain and Development

Genomic variations and chromosomal abnormalitiesEpilepsy research and treatment

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