Ogata T - Search Results

1

IMAGe syndrome: clinical and genetic implications based on investigations in three Japanese patients.

Kato F, Hamajima T, Hasegawa T, Amano N, Horikawa R, Nishimura G, Nakashima S, Fuke T, Sano S, Fukami M, Ogata T. Kato F, et al. Among authors: ogata t. Clin Endocrinol (Oxf). 2014 May;80(5):706-13. doi: 10.1111/cen.12379. Epub 2013 Dec 28. Clin Endocrinol (Oxf). 2014. PMID: 24313804

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

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

5

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

6

Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature.

Ogata T, Kosho T, Wakui K, Fukushima Y, Yoshimoto M, Miharu N. Ogata T, et al. J Clin Endocrinol Metab. 2000 Aug;85(8):2927-30. doi: 10.1210/jcem.85.8.6745. J Clin Endocrinol Metab. 2000. PMID: 10946905

7

Sex-determining gene(s) on distal 9p: clinical and molecular studies in six cases.

Muroya K, Okuyama T, Goishi K, Ogiso Y, Fukuda S, Kameyama J, Sato H, Suzuki Y, Terasaki H, Gomyo H, Wakui K, Fukushima Y, Ogata T. Muroya K, et al. Among authors: ogata t. J Clin Endocrinol Metab. 2000 Sep;85(9):3094-100. doi: 10.1210/jcem.85.9.6771. J Clin Endocrinol Metab. 2000. PMID: 10999792 Clinical Trial.

8

Novel and recurrent EBP mutations in X-linked dominant chondrodysplasia punctata.

Ikegawa S, Ohashi H, Ogata T, Honda A, Tsukahara M, Kubo T, Kimizuka M, Shimode M, Hasegawa T, Nishimura G, Nakamura Y. Ikegawa S, et al. Among authors: ogata t. Am J Med Genet. 2000 Oct 2;94(4):300-5. doi: 10.1002/1096-8628(20001002)94:4<300::aid-ajmg7>3.0.co;2-3. Am J Med Genet. 2000. PMID: 11038443 Review.

9

SHOX haploinsufficiency and overdosage: impact of gonadal function status.

Ogata T, Matsuo N, Nishimura G. Ogata T, et al. J Med Genet. 2001 Jan;38(1):1-6. doi: 10.1136/jmg.38.1.1. J Med Genet. 2001. PMID: 11134233 Free PMC article. Review.

10

Micropenis and the AR Gene: mutation and CAG repeat-length analysis.

Ishii T, Sato S, Kosaki K, Sasaki G, Muroya K, Ogata T, Matsuo N. Ishii T, et al. Among authors: ogata t. J Clin Endocrinol Metab. 2001 Nov;86(11):5372-8. doi: 10.1210/jcem.86.11.7999. J Clin Endocrinol Metab. 2001. PMID: 11701709 Clinical Trial.

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