Nodoka Hinokuma

Clinical and genetic characteristics of patients with Doose syndrome

N. Matsumoto, H. Ikeda, Y. Maegaki, 2020, Epilepsia open.

Survey of neonatal ICU nurses’ knowledge of neonatal nutrition in Japan

N. Otsuka, K. Mizuno, K. Hawthorne, 2020 .

A pediatric patient with hyponatremic hypertensive syndrome without persistent hypertension in acute phase: A case report and review of literature

K. Mizuno, Yoshifusa Abe, Shunsuke Sakurai, 2020, SAGE open medical case reports.

De novo ATP1A3 variants cause polymicrogyria

T. Tsunoda, T. Hara, A. Takata, 2021, Science Advances.

LAMA1 variants were identified Joubert syndrome patient.

M. Nakashima, Sachiko Miyamoto, M. Tominaga, 2022, Pediatrics international : official journal of the Japan Pediatric Society.