Hasegawa T - Search Results

1

Adachi M, Muroya K, Asakura Y, Kurosawa K, Nishimura G, Narumi S, Hasegawa T. Adachi M, et al. Among authors: hasegawa t. Am J Med Genet A. 2010 Jul;152A(7):1854-7. doi: 10.1002/ajmg.a.33429. Am J Med Genet A. 2010. PMID: 20583188 No abstract available.

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: hasegawa t, hasegawa y. 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

Autopsy case of microcephalic osteodysplastic primordial "dwarfism" type II.

Fukuzawa R, Sato S, Sullivan MJ, Nishimura G, Hasegawa T, Matsuo N. Fukuzawa R, et al. Among authors: hasegawa t. Am J Med Genet. 2002 Nov 15;113(1):93-6. doi: 10.1002/ajmg.10716. Am J Med Genet. 2002. PMID: 12400072

4

Microcephalic osteodysplastic primordial short stature type II with cafe-au-lait spots and moyamoya disease.

Nishimura G, Hasegawa T, Fujino M, Hori N, Tomita Y. Nishimura G, et al. Among authors: hasegawa t. Am J Med Genet A. 2003 Mar 15;117A(3):299-301. doi: 10.1002/ajmg.a.10230. Am J Med Genet A. 2003. PMID: 12599197 No abstract available.

5

Ischiospinal dysostosis with cystic kidney disease: report of two cases.

Nishimura G, Kim OH, Sato S, Hasegawa T. Nishimura G, et al. Among authors: hasegawa t. Clin Dysmorphol. 2003 Apr;12(2):101-4. doi: 10.1097/00019605-200304000-00005. Clin Dysmorphol. 2003. PMID: 12868471

6

Spondyloepiphyseal dysplasia Maroteaux type: report of three patients from two families and exclusion of type II collagen defects.

Nishimura G, Kizu R, Kijima Y, Sakai K, Kawaguchi Y, Kimura T, Matsushita I, Shirahama S, Ikeda T, Ikegawa S, Hasegawa T. Nishimura G, et al. Among authors: hasegawa t. Am J Med Genet A. 2003 Aug 1;120A(4):498-502. doi: 10.1002/ajmg.a.20095. Am J Med Genet A. 2003. PMID: 12884428

7

Newly recognized syndrome of metaphyseal undermodeling, spondylar dysplasia, and overgrowth: report of two adolescents and a child.

Nishimura G, Hasegawa T, Kinoshita E, Tanaka Y, Kurosawa K, Yoshimoto M. Nishimura G, et al. Among authors: hasegawa t. Am J Med Genet A. 2004 Jul 15;128A(2):204-8. doi: 10.1002/ajmg.a.30030. Am J Med Genet A. 2004. PMID: 15214018

8

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: hasegawa t. 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

9

Cytochrome P450 oxidoreductase deficiency in three patients initially regarded as having 21-hydroxylase deficiency and/or aromatase deficiency: diagnostic value of urine steroid hormone analysis.

Fukami M, Hasegawa T, Horikawa R, Ohashi T, Nishimura G, Homma K, Ogata T. Fukami M, et al. Among authors: hasegawa t. Pediatr Res. 2006 Feb;59(2):276-80. doi: 10.1203/01.pdr.0000195825.31504.28. Pediatr Res. 2006. PMID: 16439592

10

Growth-chart-based qualitative evaluation of height growth after hematopoietic stem cell transplantation.

Narumi S, Shimada H, Shimasaki N, Takahashi T, Hasegawa T, Mori T. Narumi S, et al. Among authors: hasegawa t. Pediatr Transplant. 2006 Feb;10(1):26-31. doi: 10.1111/j.1399-3046.2005.00388.x. Pediatr Transplant. 2006. PMID: 16499583

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