Sato N - Search Results

1

Defective jagged-1 signaling affects GnRH development and contributes to congenital hypogonadotropic hypogonadism.

Cotellessa L, Marelli F, Duminuco P, Adamo M, Papadakis GE, Bartoloni L, Sato N, Lang-Muritano M, Troendle A, Dhillo WS, Morelli A, Guarnieri G, Pitteloud N, Persani L, Bonomi M, Giacobini P, Vezzoli V. Cotellessa L, et al. Among authors: sato n. JCI Insight. 2023 Mar 8;8(5):e161998. doi: 10.1172/jci.insight.161998. JCI Insight. 2023. PMID: 36729644 Free PMC article.

2

Hypogonadotropic hypogonadism in an adult female with a heterozygous hypomorphic mutation of SOX2.

Sato N, Kamachi Y, Kondoh H, Shima Y, Morohashi K, Horikawa R, Ogata T. Sato N, et al. Eur J Endocrinol. 2007 Feb;156(2):167-71. doi: 10.1530/EJE-06-0606. Eur J Endocrinol. 2007. PMID: 17287405

3

Hypothalamic dysfunction in a female with isolated hypogonadotropic hypogonadism and compound heterozygous TACR3 mutations and clinical manifestation in her heterozygous mother.

Fukami M, Maruyama T, Dateki S, Sato N, Yoshimura Y, Ogata T. Fukami M, et al. Among authors: sato n. Horm Res Paediatr. 2010;73(6):477-81. doi: 10.1159/000313373. Epub 2010 Apr 15. Horm Res Paediatr. 2010. PMID: 20395662

4

Genetics of male hypogonadotropic hypogonadism.

Sato N. Sato N. Pediatr Endocrinol Rev. 2012 Oct;10 Suppl 1:110-25. Pediatr Endocrinol Rev. 2012. PMID: 23330252 Review. No abstract available.

5

Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols.

Sato N, Hasegawa T, Hasegawa Y, Arisaka O, Ozono K, Amemiya S, Kikuchi T, Tanaka H, Harada S, Miyata I, Tanaka T. Sato N, et al. Clin Pediatr Endocrinol. 2015 Apr;24(2):37-49. doi: 10.1297/cpe.24.37. Epub 2015 May 15. Clin Pediatr Endocrinol. 2015. PMID: 26019400 Free PMC article.

6

Kallmann syndrome phenotype in a female patient with CHARGE syndrome and CHD7 mutation.

Ogata T, Fujiwara I, Ogawa E, Sato N, Udaka T, Kosaki K. Ogata T, et al. Among authors: sato n. Endocr J. 2006 Dec;53(6):741-3. doi: 10.1507/endocrj.k06-099. Epub 2006 Sep 7. Endocr J. 2006. PMID: 16960397 Free article.

7

CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndrome.

Jongmans MC, van Ravenswaaij-Arts CM, Pitteloud N, Ogata T, Sato N, Claahsen-van der Grinten HL, van der Donk K, Seminara S, Bergman JE, Brunner HG, Crowley WF Jr, Hoefsloot LH. Jongmans MC, et al. Among authors: sato n. Clin Genet. 2009 Jan;75(1):65-71. doi: 10.1111/j.1399-0004.2008.01107.x. Epub 2008 Nov 17. Clin Genet. 2009. PMID: 19021638 Free PMC article.

8

Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadism.

Izumi Y, Suzuki E, Kanzaki S, Yatsuga S, Kinjo S, Igarashi M, Maruyama T, Sano S, Horikawa R, Sato N, Nakabayashi K, Hata K, Umezawa A, Ogata T, Yoshimura Y, Fukami M. Izumi Y, et al. Among authors: sato n. Fertil Steril. 2014 Oct;102(4):1130-1136.e3. doi: 10.1016/j.fertnstert.2014.06.017. Epub 2014 Jul 23. Fertil Steril. 2014. PMID: 25064402 Free article.

9

Kallmann syndrome: somatic and germline mutations of the fibroblast growth factor receptor 1 gene in a mother and the son.

Sato N, Ohyama K, Fukami M, Okada M, Ogata T. Sato N, et al. J Clin Endocrinol Metab. 2006 Apr;91(4):1415-8. doi: 10.1210/jc.2005-2266. Epub 2006 Jan 17. J Clin Endocrinol Metab. 2006. PMID: 16418210

10

Gonadotrophin therapy in Kallmann syndrome caused by heterozygous mutations of the gene for fibroblast growth factor receptor 1: report of three families: case report.

Sato N, Hasegawa T, Hori N, Fukami M, Yoshimura Y, Ogata T. Sato N, et al. Hum Reprod. 2005 Aug;20(8):2173-8. doi: 10.1093/humrep/dei052. Epub 2005 Apr 21. Hum Reprod. 2005. PMID: 15845591

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