Sato S - Search Results

1

Longitudinal auxological study in a female with SHOX (short stature homeobox containing gene) haploinsufficiency and normal ovarian function.

Fukami M, Matsuo N, Hasegawa T, Sato S, Ogata T. Fukami M, et al. Among authors: sato s. Eur J Endocrinol. 2003 Oct;149(4):337-41. doi: 10.1530/eje.0.1490337. Eur J Endocrinol. 2003. PMID: 14514349

2

PTPN11 (protein-tyrosine phosphatase, nonreceptor-type 11) mutations in seven Japanese patients with Noonan syndrome.

Kosaki K, Suzuki T, Muroya K, Hasegawa T, Sato S, Matsuo N, Kosaki R, Nagai T, Hasegawa Y, Ogata T. Kosaki K, et al. Among authors: sato s. J Clin Endocrinol Metab. 2002 Aug;87(8):3529-33. doi: 10.1210/jcem.87.8.8694. J Clin Endocrinol Metab. 2002. PMID: 12161469

3

Micropenis and the 5alpha-reductase-2 (SRD5A2) gene: mutation and V89L polymorphism analysis in 81 Japanese patients.

Sasaki G, Ogata T, Ishii T, Kosaki K, Sato S, Homma K, Takahashi T, Hasegawa T, Matsuo N. Sasaki G, et al. Among authors: sato s. J Clin Endocrinol Metab. 2003 Jul;88(7):3431-6. doi: 10.1210/jc.2002-021415. J Clin Endocrinol Metab. 2003. PMID: 12843198

4

Premature ovarian failure in a female with proximal symphalangism and Noggin mutation.

Kosaki K, Sato S, Hasegawa T, Matsuo N, Suzuki T, Ogata T. Kosaki K, et al. Among authors: sato s. Fertil Steril. 2004 Apr;81(4):1137-9. doi: 10.1016/j.fertnstert.2003.08.054. Fertil Steril. 2004. PMID: 15066478 Free article.

5

Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients.

Fukami M, Horikawa R, Nagai T, Tanaka T, Naiki Y, Sato N, Okuyama T, Nakai H, Soneda S, Tachibana K, Matsuo N, Sato S, Homma K, Nishimura G, Hasegawa T, Ogata T. Fukami M, et al. Among authors: sato s, sato n. J Clin Endocrinol Metab. 2005 Jan;90(1):414-26. doi: 10.1210/jc.2004-0810. Epub 2004 Oct 13. J Clin Endocrinol Metab. 2005. PMID: 15483095

6

Testosterone enanthate therapy is effective and independent of SRD5A2 and AR gene polymorphisms in boys with micropenis.

Ishii T, Sasaki G, Hasegawa T, Sato S, Matsuo N, Ogata T. Ishii T, et al. Among authors: sato s. J Urol. 2004 Jul;172(1):319-24. doi: 10.1097/01.ju.0000129005.84831.1e. J Urol. 2004. PMID: 15201804

7

A novel mutation in the FOXL2 gene in a patient with blepharophimosis syndrome: differential role of the polyalanine tract in the development of the ovary and the eyelid.

Kosaki K, Ogata T, Kosaki R, Sato S, Matsuo N. Kosaki K, et al. Among authors: sato s. Ophthalmic Genet. 2002 Mar;23(1):43-7. doi: 10.1076/opge.23.1.43.2202. Ophthalmic Genet. 2002. PMID: 11910558

8

Novel mutation of TBX3 in a Japanese family with ulnar-mammary syndrome: implication for impaired sex development.

Sasaki G, Ogata T, Ishii T, Hasegawa T, Sato S, Matsuo N. Sasaki G, et al. Among authors: sato s. Am J Med Genet. 2002 Jul 15;110(4):365-9. doi: 10.1002/ajmg.10447. Am J Med Genet. 2002. PMID: 12116211

9

Lymphstasis in a boy with Noonan syndrome: implication for the development of skeletal features.

Ogata T, Sato S, Hasegawa Y, Kosaki K. Ogata T, et al. Among authors: sato s. Endocr J. 2003 Jun;50(3):319-24. doi: 10.1507/endocrj.50.319. Endocr J. 2003. PMID: 12940461 Free article.

10

Multiple polypoid masses in the gastrointestinal tract in patient with Menkes disease on copper-histidinate therapy.

Sasaki G, Ishii T, Sato S, Hoshino K, Morikawa Y, Kodama H, Matsuo N, Takahashi T, Hasegawa T. Sasaki G, et al. Among authors: sato s. Eur J Pediatr. 2004 Dec;163(12):745-6. doi: 10.1007/s00431-004-1556-0. Eur J Pediatr. 2004. PMID: 15480778 No abstract available.

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