Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

511 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
A case of generalized lipodystrophy-associated progeroid syndrome treated by leptin replacement with short and long-term monitoring of the metabolic and endocrine profiles.
Fukaishi T, Minami I, Masuda S, Miyachi Y, Tsujimoto K, Izumiyama H, Hashimoto K, Yoshida M, Takahashi S, Kashimada K, Morio T, Kosaki K, Maezawa Y, Yokote K, Yoshimoto T, Yamada T. Fukaishi T, et al. Among authors: kosaki k. Endocr J. 2020 Feb 28;67(2):211-218. doi: 10.1507/endocrj.EJ19-0226. Epub 2019 Nov 8. Endocr J. 2020. PMID: 31708526 Free article.
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. Hozumi K, et al. Among authors: kosaki k. Endocr J. 2019 Oct 28;66(10):853-857. doi: 10.1507/endocrj.EJ19-0035. Epub 2019 Jun 12. Endocr J. 2019. PMID: 31189769 Free article.
Clinical report: Chronic liver dysfunction in an individual with an AMOTL1 variant.
Kirino S, Suzuki M, Ogawa T, Takasawa K, Adachi E, Gau M, Takahashi K, Ikeno M, Yamada M, Suzuki H, Kosaki K, Moriyama K, Yoshida M, Morio T, Kashimada K. Kirino S, et al. Among authors: kosaki k. Eur J Med Genet. 2022 Nov;65(11):104623. doi: 10.1016/j.ejmg.2022.104623. Epub 2022 Sep 15. Eur J Med Genet. 2022. PMID: 36116699
BMP2 is a potential causative gene for isolated dextrocardia situs solitus.
Yogi A, Iemura R, Nakatani H, Takasawa K, Gau M, Yamauchi T, Yoshida M, Moriyama K, Ishii T, Hosokawa S, Yamada M, Suzuki H, Kosaki K, Kashimada K, Morio T. Yogi A, et al. Among authors: kosaki k. Eur J Med Genet. 2023 Sep;66(9):104820. doi: 10.1016/j.ejmg.2023.104820. Epub 2023 Aug 11. Eur J Med Genet. 2023. PMID: 37572998
Case report: Adult phenotype of Mulvihill-Smith syndrome.
Yagihashi T, Kato M, Izumi K, Kosaki R, Yago K, Tsubota K, Sato Y, Okubo M, Watanabe G, Takahashi T, Kosaki K. Yagihashi T, et al. Among authors: kosaki r, kosaki k. Am J Med Genet A. 2009 Mar;149A(3):496-500. doi: 10.1002/ajmg.a.32551. Am J Med Genet A. 2009. PMID: 19213035
511 results