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Fingerprint Dive into the research topics where Takeshi Sato is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 1 Similar Profiles
Mutation Medicine & Life Sciences
Primary Hyperparathyroidism Medicine & Life Sciences
Septo-Optic Dysplasia Medicine & Life Sciences
Genes Medicine & Life Sciences
Multiple Endocrine Neoplasia Type 1 Medicine & Life Sciences
Anti-N-Methyl-D-Aspartate Receptor Encephalitis Medicine & Life Sciences
Growth Hormone-Secreting Pituitary Adenoma Medicine & Life Sciences
Pediatrics Medicine & Life Sciences

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Research Output 2012 2019

  • 57 Citations
  • 6 h-Index
  • 16 Article
  • 1 Comment/debate

A case report and literature review of monoallelic mutation of GHR

Mitani, M., Shima, H., Sato, T., Inoguchi, T., Kamimaki, T., Fukami, M. & Hasegawa, T., 2019 Jan 1, In : Journal of Pediatric Endocrinology and Metabolism.

Research output: Contribution to journalArticle

Missense Mutation
Insulin-Like Growth Factor I
Computer Simulation
Growth Hormone

Acromegaly caused by a somatotroph adenoma in patient with neurofibromatosis type 1

Hozumi, K., Fukuoka, H., Odake, Y., Takeuchi, T., Uehara, T., Sato, T., Inoshita, N., Yoshida, K., Matsumoto, R., Bando, H., Hirota, Y., Iguchi, G., Taniguchi, M., Otsuki, N., Nishigori, C., Kosaki, K., Hasegawa, T., Ogawa, W. & Takahashi, Y., 2019 Jan 1, In : Endocrine journal. 66, 10, p. 853-857 5 p.

Research output: Contribution to journalArticle

Open Access
Growth Hormone-Secreting Pituitary Adenoma
Neurofibromatosis 1
Neurofibromatosis 1 Genes
Follicular Adenocarcinoma

A Familial Case of a Whole Germline CDC73 Deletion Discordant for Primary Hyperparathyroidism

Hatabu, N., Katori, N., Sato, T., Maeda, N., Suzuki, E., Komiyama, O., Tsutsui, H., Nagao, T., Nakauchi-Takahashi, H., Matsunaga, T., Ishii, T., Hasegawa, T. & Yamazawa, K., 2019 Jan 1, In : Hormone Research in Paediatrics.

Research output: Contribution to journalArticle

Primary Hyperparathyroidism
Parathyroid Neoplasms
1 Citation (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 Jan 1, In : Clinical Pediatric Endocrinology. 27, 3, p. 197-199 3 p.

Research output: Contribution to journalComment/debate

Multiple Endocrine Neoplasia Type 1

A pediatric case of pheochromocytoma without apparent hypertension associated with von hippel-lindau disease

Igaki, J., Nishi, A., Sato, T. & Hasegawa, T., 2018 Jan 1, In : Clinical Pediatric Endocrinology. 27, 2, p. 87-93 7 p.

Research output: Contribution to journalArticle

von Hippel-Lindau Disease