Acquired uniparental disomy of chromosome 7 in a patient with MIRAGE syndrome that veiled a pathogenic SAMD9 variant

por Tanase-Nakao, Kanako, Kawai, Masanobu, Wada, Kazuko, Kagami, Masayo, Narumi, Satoshi
Publicado 2021

A patient with congenital hypothyroidism due to a PAX8 frameshift variant accompanying a urogenital malformation

por Tanase-Nakao, Kanako, Muroya, Koji, Adachi, Masanori, Abe, Kiyomi, Hasegawa, Tomonobu, Narumi, Satoshi
Publicado 2022

The case of a patient with MIRAGE syndrome with familial dysautonomia-like symptoms

por Kawashima-Sonoyama, Yuki, Okuno, Keisuke, Dohmoto, Tomotsune, Tanase-Nakao, Kanako, Narumi, Satoshi, Namba, Noriyuki
Publicado 2021

Potential protective effect of lactation against incidence of type 2 diabetes mellitus in women with previous gestational diabetes mellitus: A systematic review and meta‐analysis

por Tanase‐Nakao, Kanako, Arata, Naoko, Kawasaki, Maki, Yasuhi, Ichiro, Sone, Hirohito, Mori, Rintaro, Ota, Erika
Publicado 2017

A girl with MIRAGE syndrome who developed steroid-resistant nephrotic syndrome: a case report

por Ishiwa, Sho, Kamei, Koichi, Tanase-Nakao, Kanako, Shibata, Shinsuke, Matsunami, Kunihiro, Takeuchi, Ichiro, Sato, Mai, Ishikura, Kenji, Narumi, Satoshi
Publicado 2020

A case report with functional characterization of a HNF1B mutation (p.Leu168Pro) causing MODY5

por Yoshida, Kei, Mushimoto, Yuichi, Tanase-Nakao, Kanako, Akiba, Kazuhisa, Ishii, Kanako, Urakami, Tatsuhiko, Sugihara, Shigetaka, Kikuchi, Toru, Fukami, Maki, Narumi, Satoshi
Publicado 2021

MIRAGE syndrome caused by a novel missense variant (p.Ala1479Ser) in the SAMD9 gene

por Onuma, Shinsuke, Wada, Tamaki, Araki, Ryosuke, Wada, Kazuko, Tanase-Nakao, Kanako, Narumi, Satoshi, Fukui, Miho, Shoji, Yasuko, Etani, Yuri, Ida, Shinobu, Kawai, Masanobu
Publicado 2020

Primary hyperparathyroidism due to atypical vertically long cystic adenoma

por Kawashima, Sachiko-Tsukamoto, Usui, Takeshi, Ueda, Yohei, Kobayashi, Maiko-Kakita, Tsuiki, Mika, Tanase-Nakao, Kanako, Nanba, Kazutaka, Tagami, Tetsuya, Naruse, Mitsuhide, Watanabe, Yoshiki, Asato, Ryo, Kato, Sumiko, Shimatsu, Akira
Publicado 2014

Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients

por Inoue, Takanobu, Nakamura, Akie, Iwahashi-Odano, Megumi, Tanase-Nakao, Kanako, Matsubara, Keiko, Nishioka, Junko, Maruo, Yoshihiro, Hasegawa, Yukihiro, Suzumura, Hiroshi, Sato, Seiji, Kobayashi, Yoshiyuki, Murakami, Nobuyuki, Nakabayashi, Kazuhiko, Yamazawa, Kazuki, Fuke, Tomoko, Narumi, Satoshi, Oka, Akira, Ogata, Tsutomu, Fukami, Maki, Kagami, Masayo
Publicado 2020