• 5795 引用
  • 39 h指数
1986 …2020

年単位の研究成果

Pureに変更を加えた場合、すぐここに表示されます。

研究成果

フィルター
Comment/debate
2018

A familial case of spondyloepiphyseal dysplasia tarda caused by a novel splice site mutation in TRAPPC2

Fukuma, M., Takagi, M., Shimazu, T., Imamura, H., Yagi, H., Nishimura, G. & Hasegawa, T., 2018, : : clinical pediatric endocrinology. 27, 3, p. 193-196 4 p.

研究成果: Comment/debate

3 引用 (Scopus)

A pediatric case of insulinoma and a novel MEN1 mutation: The efficacy of the combination therapy of diazoxide and cornstarch

Nakano, S., Sato, T., Hosokawa, M., Takagi, C., Yoshida, F., Ishii, T., Sato, S. & Hasegawa, T., 2018, : : clinical pediatric endocrinology. 27, 3, p. 197-199 3 p.

研究成果: Comment/debate

1 引用 (Scopus)
2017

A novel heterozygous intronic mutation in POU1F1 is associated with combined pituitary hormone deficiency

Takagi, M., Kamasaki, H., Yagi, H., Fukuzawa, R., Narumi, S. & Hasegawa, T., 2017, : : Endocrine Journal. 64, 2, p. 229-234 6 p.

研究成果: Comment/debate

3 引用 (Scopus)
2016

A novel mutation in HESX1 causes combined pituitary hormone deficiency without septo optic dysplasia phenotypes

Takagi, M., Takahashi, M., Ohtsu, Y., Sato, T., Narumi, S., Arakawa, H. & Hasegawa, T., 2016 4 25, : : Endocrine journal. 63, 4, p. 405-410 6 p.

研究成果: Comment/debate

10 引用 (Scopus)
2011
2 引用 (Scopus)
2010
8 引用 (Scopus)
2007

Erratum: Cxorf6 is a causative gene for hypospadias (Nature Genetics (2006) 38, (1369-1371))

Fukami, M., Wada, Y., Miyabayashi, K., Nishino, I., Hasegawa, T., Camerino, G., Kretz, C., Buj-Bello, A., Laporte, J., Yamada, G., Morohashi, K. I. & Ogata, T., 2007 1 1, : : Nature genetics. 39, 1, 1 p.

研究成果: Comment/debate

1 引用 (Scopus)
1997
1 引用 (Scopus)