Ogata T - Search Results

1

Growth hormone secretion and its effect on height in pediatric patients with different genotypes of Prader-Willi syndrome.

Oto Y, Obata K, Matsubara K, Kozu Y, Tsuchiya T, Sakazume S, Yoshino A, Murakami N, Ogata T, Nagai T. Oto Y, et al. Among authors: ogata t. Am J Med Genet A. 2012 Jun;158A(6):1477-80. doi: 10.1002/ajmg.a.35378. Epub 2012 May 14. Am J Med Genet A. 2012. PMID: 22585665

2

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

3

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

4

Genetic evidence for a novel gene(s) involved in urogenital development on 10q26.

Ogata T, Muroya K, Sasagawa I, Kosho T, Wakui K, Sakazume S, Ito K, Matsuo N, Ohashi H, Nagai T. Ogata T, et al. Kidney Int. 2000 Dec;58(6):2281-90. doi: 10.1046/j.1523-1755.2000.00412.x. Kidney Int. 2000. PMID: 11115062 Free article.

5

GATA3 abnormalities and the phenotypic spectrum of HDR syndrome.

Muroya K, Hasegawa T, Ito Y, Nagai T, Isotani H, Iwata Y, Yamamoto K, Fujimoto S, Seishu S, Fukushima Y, Hasegawa Y, Ogata T. Muroya K, et al. Among authors: ogata t. J Med Genet. 2001 Jun;38(6):374-80. doi: 10.1136/jmg.38.6.374. J Med Genet. 2001. PMID: 11389161 Free PMC article.

6

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: ogata t. J Clin Endocrinol Metab. 2002 Aug;87(8):3529-33. doi: 10.1210/jcem.87.8.8694. J Clin Endocrinol Metab. 2002. PMID: 12161469

7

Sotos syndrome and haploinsufficiency of NSD1: clinical features of intragenic mutations and submicroscopic deletions.

Nagai T, Matsumoto N, Kurotaki N, Harada N, Niikawa N, Ogata T, Imaizumi K, Kurosawa K, Kondoh T, Ohashi H, Tsukahara M, Makita Y, Sugimoto T, Sonoda T, Yokoyama T, Uetake K, Sakazume S, Fukushima Y, Naritomi K. Nagai T, et al. Among authors: ogata t. J Med Genet. 2003 Apr;40(4):285-9. doi: 10.1136/jmg.40.4.285. J Med Genet. 2003. PMID: 12676901 Free PMC article. No abstract available.

8

Fifty microdeletions among 112 cases of Sotos syndrome: low copy repeats possibly mediate the common deletion.

Kurotaki N, Harada N, Shimokawa O, Miyake N, Kawame H, Uetake K, Makita Y, Kondoh T, Ogata T, Hasegawa T, Nagai T, Ozaki T, Touyama M, Shenhav R, Ohashi H, Medne L, Shiihara T, Ohtsu S, Kato Z, Okamoto N, Nishimoto J, Lev D, Miyoshi Y, Ishikiriyama S, Sonoda T, Sakazume S, Fukushima Y, Kurosawa K, Cheng JF, Yoshiura K, Ohta T, Kishino T, Niikawa N, Matsumoto N. Kurotaki N, et al. Among authors: ogata t. Hum Mutat. 2003 Nov;22(5):378-87. doi: 10.1002/humu.10270. Hum Mutat. 2003. PMID: 14517949

9

Statural growth in 31 Japanese patients with SHOX haploinsufficiency: support for a disadvantageous effect of gonadal estrogens.

Fukami M, Nishi Y, Hasegawa Y, Miyoshi Y, Okabe T, Haga N, Nagai T, Tanaka T, Ogata T. Fukami M, et al. Among authors: ogata t. Endocr J. 2004 Apr;51(2):197-200. doi: 10.1507/endocrj.51.197. Endocr J. 2004. PMID: 15118270 Free article.

10

A 3-bp deletion mutation of PTPN11 in an infant with severe Noonan syndrome including hydrops fetalis and juvenile myelomonocytic leukemia.

Yoshida R, Miyata M, Nagai T, Yamazaki T, Ogata T. Yoshida R, et al. Among authors: ogata t. Am J Med Genet A. 2004 Jul 1;128A(1):63-6. doi: 10.1002/ajmg.a.30029. Am J Med Genet A. 2004. PMID: 15211660

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