Ogata T - Search Results

1

Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.

Sato N, Katsumata N, Kagami M, Hasegawa T, Hori N, Kawakita S, Minowada S, Shimotsuka A, Shishiba Y, Yokozawa M, Yasuda T, Nagasaki K, Hasegawa D, Hasegawa Y, Tachibana K, Naiki Y, Horikawa R, Tanaka T, Ogata T. Sato N, et al. Among authors: ogata t. J Clin Endocrinol Metab. 2004 Mar;89(3):1079-88. doi: 10.1210/jc.2003-030476. J Clin Endocrinol Metab. 2004. PMID: 15001591

2

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

3

Further clinical model for the possible impairment of a putative lymphogenic gene(s) for Turner stigmata.

Ogata T, Hasegawa T, Matsuo N. Ogata T, et al. Hum Genet. 1997 Feb;99(2):290. doi: 10.1007/s004390050358. Hum Genet. 1997. PMID: 9048940 No abstract available.

4

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

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

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.

7

Del(X)(p21.1) in a mother and two daughters: genotype-phenotype correlation of Turner features.

Adachi M, Tachibana K, Asakura Y, Muroya K, Ogata T. Adachi M, et al. Among authors: ogata t. Hum Genet. 2000 Mar;106(3):306-10. doi: 10.1007/s004390051042. Hum Genet. 2000. PMID: 10798359

8

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

9

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.

10

Clinical and molecular studies in 15 females with ring X chromosomes: implications for r(X) formation and mental development.

Matsuo M, Muroya K, Adachi M, Tachibana K, Asakura Y, Nakagomi Y, Hanaki K, Yokoya S, Yoshizawa A, Igarashi Y, Hanew K, Matsuo N, Ogata T. Matsuo M, et al. Among authors: ogata t. Hum Genet. 2000 Nov;107(5):433-9. doi: 10.1007/s004390000377. Hum Genet. 2000. PMID: 11140940

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