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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
Anti-N-Methyl-D-Aspartate Receptor Encephalitis Medicine & Life Sciences
Pediatrics Medicine & Life Sciences
Maple Syrup Urine Disease Medicine & Life Sciences
Hypophosphatemic Rickets Medicine & Life Sciences

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Research Output 2012 2019

  • 52 Citations
  • 6 h-Index
  • 15 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

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

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
Genes
Hypophosphatemia
Parathyroid Neoplasms
Parathyroidectomy

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
Diazoxide
Insulinoma
Starch
Pediatrics

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
Pheochromocytoma
Pediatrics
Hypertension
Tachycardia
10 Citations (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 Apr 25, In : Endocrine Journal. 63, 4, p. 405-410 6 p.

Research output: Contribution to journalArticle

Septo-Optic Dysplasia
Phenotype
Mutation
Pituitary Dwarfism
Adrenal Insufficiency