Matsuo N - 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: matsuo n. 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: matsuo n. 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: matsuo n. 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: matsuo n. 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: matsuo 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

WHO 2006 Child Growth Standards overestimate short stature and underestimate overweight in Japanese children.

Inokuchi M, Matsuo N, Takayama JI, Hasegawa T. Inokuchi M, et al. Among authors: matsuo n. J Pediatr Endocrinol Metab. 2018 Jan 26;31(1):33-38. doi: 10.1515/jpem-2017-0303. J Pediatr Endocrinol Metab. 2018. PMID: 29267170 Free article.

7

Population-based waist circumference reference values in Japanese children (0-6 years): comparisons with Dutch, Swedish and Turkish preschool children.

Inokuchi M, Matsuo N, Takayama JI, Hasegawa T. Inokuchi M, et al. Among authors: matsuo n. J Pediatr Endocrinol Metab. 2020 Dec 18;34(3):349-356. doi: 10.1515/jpem-2020-0418. Print 2021 Mar 26. J Pediatr Endocrinol Metab. 2020. PMID: 33675207 Free article.

8

Reference values of inside leg length and inside leg length to stature ratio for Japanese children, 0-12 years of age.

Inokuchi M, Matsuo N, Takayama JI, Hasegawa T. Inokuchi M, et al. Among authors: matsuo n. Ann Hum Biol. 2022 Feb;49(1):1-9. doi: 10.1080/03014460.2022.2045355. Epub 2022 Mar 17. Ann Hum Biol. 2022. PMID: 35191816 Free article.

9

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: matsuo n. Ophthalmic Genet. 2002 Mar;23(1):43-7. doi: 10.1076/opge.23.1.43.2202. Ophthalmic Genet. 2002. PMID: 11910558

10

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: matsuo n. Am J Med Genet. 2002 Jul 15;110(4):365-9. doi: 10.1002/ajmg.10447. Am J Med Genet. 2002. PMID: 12116211

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