Ogata T - Search Results

1

Cytochrome P450 oxidoreductase deficiency: identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patients.

Fukami M, Nishimura G, Homma K, Nagai T, Hanaki K, Uematsu A, Ishii T, Numakura C, Sawada H, Nakacho M, Kowase T, Motomura K, Haruna H, Nakamura M, Ohishi A, Adachi M, Tajima T, Hasegawa Y, Hasegawa T, Horikawa R, Fujieda K, Ogata T. Fukami M, et al. Among authors: ogata t. J Clin Endocrinol Metab. 2009 May;94(5):1723-31. doi: 10.1210/jc.2008-2816. Epub 2009 Mar 3. J Clin Endocrinol Metab. 2009. PMID: 19258400

2

Oto-palato-digital syndrome, type II: evidence for defective intramembranous ossification.

Ogata T, Matsuo N, Nishimura G, Hajikano H. Ogata T, et al. Am J Med Genet. 1990 Jun;36(2):226-31. doi: 10.1002/ajmg.1320360217. Am J Med Genet. 1990. PMID: 2114799

3

Coarctation of the aorta and renal hypoplasia in a boy with Turner/Noonan surface anomalies and a 46,XY karyotype: a clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner somatic stigmata.

Hasegawa T, Ogata T, Hasegawa Y, Honda M, Nagai T, Fukushima Y, Nakahori Y, Matsuo N. Hasegawa T, et al. Among authors: ogata t. Hum Genet. 1996 May;97(5):564-7. doi: 10.1007/BF02281861. Hum Genet. 1996. PMID: 8655131

4

Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: implication for the MRX locus.

Muroya K, Ogata T, Matsuo N, Nagai T, Franco B, Ballabio A, Rappold G, Sakura N, Fukushima Y. Muroya K, et al. Among authors: ogata t. Am J Med Genet. 1996 Sep 6;64(4):583-7. doi: 10.1002/(SICI)1096-8628(19960906)64:4<583::AID-AJMG11>3.0.CO;2-D. Am J Med Genet. 1996. PMID: 8870926

5

A case of skeletal dysplasia with advanced carpal ossification and "monkey wrench" appearance of the femora: mild Desbuquois dysplasia?

Nishimura G, Sato S, Ogata T, Tamai S, Hasegawa T, Matsuo N. Nishimura G, et al. Among authors: ogata t. Eur J Pediatr. 1996 Dec;155(12):1040-2. doi: 10.1007/BF02532527. Eur J Pediatr. 1996. PMID: 8956941

6

Hypergonadotropic hypogonadism in a 3-year-old girl with blepharophimosis, ptosis, and epicanthus inversus syndrome.

Ogata T, Hasegawa T, Tamai S, Sato S, Hasegawa Y, Matsuo N. Ogata T, et al. Horm Res. 1998 Sep;50(3):190-2. doi: 10.1159/000023272. Horm Res. 1998. PMID: 9762009

7

Gonadoblastoma, mixed germ cell tumor, and Y chromosomal genotype: molecular analysis in four patients.

Muroya K, Ishii T, Nakahori Y, Asakura Y, Tachibana K, Masuno M, Imaizumi K, Tanaka Y, Kawada Y, Yukizane S, Ogata T. Muroya K, et al. Among authors: ogata t. Genes Chromosomes Cancer. 1999 May;25(1):40-5. doi: 10.1002/(sici)1098-2264(199905)25:1<40::aid-gcc6>3.0.co;2-8. Genes Chromosomes Cancer. 1999. PMID: 10221338

8

Random X-inactivation in a girl with duplication Xp11.21-p21.3: report of a patient and review of the literature.

Matsuo M, Muroya K, Kosaki K, Ishii T, Fukushima Y, Anzo M, Ogata T. Matsuo M, et al. Among authors: ogata t. Am J Med Genet. 1999 Sep 3;86(1):44-50. Am J Med Genet. 1999. PMID: 10440827 Review.

9

Skeletal features and growth patterns in 14 patients with haploinsufficiency of SHOX: implications for the development of Turner syndrome.

Kosho T, Muroya K, Nagai T, Fujimoto M, Yokoya S, Sakamoto H, Hirano T, Terasaki H, Ohashi H, Nishimura G, Sato S, Matsuo N, Ogata T. Kosho T, et al. Among authors: ogata t. J Clin Endocrinol Metab. 1999 Dec;84(12):4613-21. doi: 10.1210/jcem.84.12.6289. J Clin Endocrinol Metab. 1999. PMID: 10599728

10

Mother and daughter with 45,X/46,X,r(X)(p22.3q28) and mental retardation: analysis of the X-inactivation patterns.

Matsuo M, Muroya K, Nanao K, Hasegawa Y, Terasaki H, Kosaki K, Ogata T. Matsuo M, et al. Among authors: ogata t. Am J Med Genet. 2000 Apr 10;91(4):267-72. Am J Med Genet. 2000. PMID: 10766981 Review.

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