A case of transient neonatal diabetes due to a novel mutation in ABCC8

por Takagi, Masaki, Takeda, Ryojun, Yagi, Hiroko, Ariyasu, Daisuke, Fukuzawa, Ryuji, Hasegawa, Tomonobu
Publicado 2016

An association with hypopituitarism and 9q subtelomere deletion syndrome

por Higuchi, Shinji, Takagi, Masaki, Takeda, Ryojun, Yoshihashi, Hiroshi, Narumi, Satoshi, Hasegawa, Tomonobu
Publicado 2018

A case of a Japanese patient with neonatal diabetes mellitus caused by a novel mutation in the ABCC8 gene and successfully controlled with oral glibenclamide

por Takeda, Ryojun, Takagi, Masaki, Miyai, Kentaro, Shinohara, Hiroyuki, Yagi, Hiroko, Moritani, Maki, Yokota, Ichiro, Hasegawa, Yukihiro
Publicado 2015

A case of spondyloepiphyseal dysplasia tarda caused by a novel intragenic deletion of TRAPPC2

por Takagi, Masaki, Yagi, Hiroko, Nakamura, Yoshie, Shinohara, Hiroyuki, Takeda, Ryojun, Shimada, Aya, Nishimura, Gen, Hasegawa, Yukihiro
Publicado 2015

Efficacy and Safety of Denosumab Therapy for Osteogenesis Imperfecta Patients with Osteoporosis—Case Series

por Kobayashi, Tsukasa, Nakamura, Yukio, Suzuki, Takako, Yamaguchi, Tomomi, Takeda, Ryojun, Takagi, Masaki, Hasegawa, Tomonobu, Kosho, Tomoki, Kato, Hiroyuki
Publicado 2018

Clinical and molecular features of patients with COL1 ‐related disorders: Implications for the wider spectrum and the risk of vascular complications

por Takeda, Ryojun, Yamaguchi, Tomomi, Hayashi, Shujiro, Sano, Shinichirou, Kawame, Hiroshi, Kanki, Sachiko, Taketani, Takeshi, Yoshimura, Hidekane, Nakamura, Yukio, Kosho, Tomoki
Publicado 2022