Ogata T - Search Results

1

Efficacy and safety of GH treatment in Japanese children with short stature due to SHOX deficiency: a randomized phase 3 study.

Ogata T, Fukami M, Tanizawa K, Yamamoto T, Sato Y, Hirai H, Takasao N, Ibaraki R, Noda M. Ogata T, et al. Clin Pediatr Endocrinol. 2024;33(2):43-49. doi: 10.1297/cpe.2023-0070. Epub 2024 Jan 28. Clin Pediatr Endocrinol. 2024. PMID: 38572386 Free PMC article.

2

Skeletal Deformity Associated with SHOX Deficiency.

Seki A, Jinno T, Suzuki E, Takayama S, Ogata T, Fukami M. Seki A, et al. Among authors: ogata t. Clin Pediatr Endocrinol. 2014 Jul;23(3):65-72. doi: 10.1297/cpe.23.65. Epub 2014 Aug 6. Clin Pediatr Endocrinol. 2014. PMID: 25110390 Free PMC article. Review.

3

Longitudinal auxological study in a female with SHOX (short stature homeobox containing gene) haploinsufficiency and normal ovarian function.

Fukami M, Matsuo N, Hasegawa T, Sato S, Ogata T. Fukami M, et al. Among authors: ogata t. Eur J Endocrinol. 2003 Oct;149(4):337-41. doi: 10.1530/eje.0.1490337. Eur J Endocrinol. 2003. PMID: 14514349

4

OTX2 mutation in a patient with anophthalmia, short stature, and partial growth hormone deficiency: functional studies using the IRBP, HESX1, and POU1F1 promoters.

Dateki S, Fukami M, Sato N, Muroya K, Adachi M, Ogata T. Dateki S, et al. Among authors: ogata t. J Clin Endocrinol Metab. 2008 Oct;93(10):3697-702. doi: 10.1210/jc.2008-0720. Epub 2008 Jul 15. J Clin Endocrinol Metab. 2008. PMID: 18628516

5

MAMLD1 (CXorf6) is a New Gene for Hypospadias.

Ogata T, Fukami M, Wada Y. Ogata T, et al. Clin Pediatr Endocrinol. 2008;17(4):87-93. doi: 10.1297/cpe.17.87. Epub 2008 Nov 8. Clin Pediatr Endocrinol. 2008. PMID: 24790369 Free PMC article. Review.

6

Cytochrome P450 oxidoreductase deficiency: rare congenital disorder leading to skeletal malformations and steroidogenic defects.

Fukami M, Ogata T. Fukami M, et al. Among authors: ogata t. Pediatr Int. 2014 Dec;56(6):805-808. doi: 10.1111/ped.12518. Pediatr Int. 2014. PMID: 25294558 Review.

7

SHOX Haploinsufficiency as a Cause of Syndromic and Nonsyndromic Short Stature.

Fukami M, Seki A, Ogata T. Fukami M, et al. Among authors: ogata t. Mol Syndromol. 2016 Apr;7(1):3-11. doi: 10.1159/000444596. Epub 2016 Mar 15. Mol Syndromol. 2016. PMID: 27194967 Free PMC article. Review.

8

Classic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in Japanese infants by urinary steroid metabolites.

Koyama Y, Homma K, Fukami M, Miwa M, Ikeda K, Ogata T, Murata M, Hasegawa T. Koyama Y, et al. Among authors: ogata t. Clin Pediatr Endocrinol. 2016 Apr;25(2):37-44. doi: 10.1297/cpe.25.37. Epub 2016 Apr 28. Clin Pediatr Endocrinol. 2016. PMID: 27212795 Free PMC article.

9

SHOX far-downstream deletion in a patient with nonsyndromic short stature.

Fukami M, Shindo J, Ogata T, Kageyama I, Kamimaki T. Fukami M, et al. Among authors: ogata t. Am J Med Genet A. 2022 Jul;188(7):2173-2177. doi: 10.1002/ajmg.a.62734. Epub 2022 Mar 23. Am J Med Genet A. 2022. PMID: 35319168

10

[Leri-Weill syndrome].

Ogata T, Fukami M. Ogata T, et al. Nihon Rinsho. 2006 Sep 28;Suppl 3:427-32. Nihon Rinsho. 2006. PMID: 17022580 Review. Japanese. No abstract available.

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