Tsunanori Shidei
发表
T. Morio,
Masatoshi Kondo,
K. Kashimada,
2022,
Scientific Reports.
Marked clinical heterogeneity in congenital hyperinsulinism due to a novel homozygous ABCC8 mutation
T. Morio,
K. Kashimada,
Ryuichi Nakagawa,
2021,
Clinical endocrinology.
T. Morio,
K. Kashimada,
Chikako Morioka,
2022,
Pediatrics international : official journal of the Japan Pediatric Society.