年別の研究成果
年別の研究成果
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Comment/debate
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, In: clinical pediatric endocrinology. 27, 3, p. 193-196 4 p.研究成果: Comment/debate › 査読
Open Access3 被引用数 (Scopus) -
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, In: Endocrine journal. 64, 2, p. 229-234 6 p.研究成果: Comment/debate › 査読
Open Access10 被引用数 (Scopus) -
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月 25, In: Endocrine journal. 63, 4, p. 405-410 6 p.研究成果: Comment/debate › 査読
Open Access12 被引用数 (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, In: clinical pediatric endocrinology. 27, 3, p. 197-199 3 p.研究成果: Comment/debate › 査読
1 被引用数 (Scopus) -
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月, In: Nature genetics. 39, 1, p. 131 1 p.研究成果: Comment/debate › 査読
1 被引用数 (Scopus) -
Free cortisol/cortisone ratio in pooled urine was increased after rapid-ACTH stimulation test under dexamethasone suppression
Koyama, Y., Homma, K., Murata, M., Shibata, H., Itoh, H. & Hasegawa, T., 2011, In: Endocrine journal. 58, 12, p. 1099-1103 5 p.研究成果: Comment/debate › 査読
2 被引用数 (Scopus) -
Further clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner stigmata.
Ogata, T., Hasegawa, T. & Matsuo, N., 1997 2月, In: Human genetics. 99, 2, 1 p.研究成果: Comment/debate › 査読
1 被引用数 (Scopus) -
Unilateral adrenalectomy can be an alternative therapy for infantile onset Cushing's syndrome caused by ACTH-independent macronodular adrenal hyperplasia with McCune-Albright syndrome
Hamajima, T., Maruwaka, K., Homma, K., Matsuo, K., Fujieda, K. & Hasegawa, T., 2010, In: Endocrine journal. 57, 9, p. 819-824 6 p.研究成果: Comment/debate › 査読
10 被引用数 (Scopus)