• 5534 Citations
  • 39 h-Index
1986 …2019
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Fingerprint Dive into the research topics where Tomonobu Hasegawa is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 5 Similar Profiles
Mutation Medicine & Life Sciences
Genes Medicine & Life Sciences
Growth Hormone Medicine & Life Sciences
Insulin-Like Growth Factor I Medicine & Life Sciences
Congenital Hypothyroidism Medicine & Life Sciences
Insulin-Like Growth Factor Binding Protein 3 Medicine & Life Sciences
Japan Medicine & Life Sciences
Phenotype Medicine & Life Sciences

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Research Output 1986 2019

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
Hematopoietic Stem Cell Transplantation
Metabolic Diseases
Lipodystrophy
Graft vs Host Disease
Fats

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
Acromegaly
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
Genes
Hypophosphatemia
Parathyroid Neoplasms
Parathyroidectomy

A neonatal case of HDR syndrome and a vascular ring with a novel GATA3 mutation

Kusakawa, M., Sato, T., Hosoda, A., Araki, E., Matsuzaki, Y., Yamashita, Y., Ishihara, J., Inagaki, Y., Uchida, N., Ishii, T. & Hasegawa, T., 2019 Dec 1, In : Human Genome Variation. 6, 1, 55.

Research output: Contribution to journalArticle

Open Access
Blood Vessels
Genes
Mutation
Genetic Databases
Haploinsufficiency