Tajima T - Search Results

1

Identification and functional analysis of novel calcium-sensing receptor gene mutation in familial hypocalciuric hypercalcemia.

Nanjo K, Nagai S, Shimizu C, Tajima T, Kondo T, Miyoshi H, Yoshioka N, Koike T. Nanjo K, et al. Among authors: tajima t. Endocr J. 2010;57(9):787-92. doi: 10.1507/endocrj.k10e-178. Epub 2010 Aug 6. Endocr J. 2010. PMID: 20697181 Free article.

2

Two novel mutations of thiazide-sensitive Na-Cl cotrans porter (TSC) gene in two sporadic Japanese patients with Gitelman syndrome.

Tajima T, Kobayashi Y, Abe S, Takahashi M, Konno M, Nakae J, Okuhara K, Satoh K, Ishikawa T, Imai T, Fujieda K. Tajima T, et al. Endocr J. 2002 Feb;49(1):91-6. doi: 10.1507/endocrj.49.91. Endocr J. 2002. PMID: 12008755 Free article.

3

Hydrochlorothiazide effectively reduces urinary calcium excretion in two Japanese patients with gain-of-function mutations of the calcium-sensing receptor gene.

Sato K, Hasegawa Y, Nakae J, Nanao K, Takahashi I, Tajima T, Shinohara N, Fujieda K. Sato K, et al. Among authors: tajima t. J Clin Endocrinol Metab. 2002 Jul;87(7):3068-73. doi: 10.1210/jcem.87.7.8639. J Clin Endocrinol Metab. 2002. PMID: 12107202

4

Two novel aquaporin-2 mutations in a sporadic Japanese patient with autosomal recessive nephrogenic diabetes insipidus.

Tajima T, Okuhara K, Satoh K, Nakae J, Fujieda K. Tajima T, et al. Endocr J. 2003 Aug;50(4):473-6. doi: 10.1507/endocrj.50.473. Endocr J. 2003. PMID: 14599123 Free article.

5

Two novel mutations in the thyroid peroxidase gene with goitrous hypothyroidism.

Tajima T, Tsubaki J, Fujieda K. Tajima T, et al. Endocr J. 2005 Oct;52(5):643-5. doi: 10.1507/endocrj.52.643. Endocr J. 2005. PMID: 16284446 Free article.

6

Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndrome.

Tajima T, Nawate M, Takahashi Y, Mizoguchi Y, Sugihara S, Yoshimoto M, Murakami M, Adachi M, Tachibana K, Mochizuki H, Fujieda K. Tajima T, et al. Endocr J. 2006 Oct;53(5):647-52. doi: 10.1507/endocrj.k06-034. Epub 2006 Aug 11. Endocr J. 2006. PMID: 16902263 Free article.

7

A novel missense mutation (P366T) of the LHX4 gene causes severe combined pituitary hormone deficiency with pituitary hypoplasia, ectopic posterior lobe and a poorly developed sella turcica.

Tajima T, Hattori T, Nakajima T, Okuhara K, Tsubaki J, Fujieda K. Tajima T, et al. Endocr J. 2007 Aug;54(4):637-41. doi: 10.1507/endocrj.k06-200. Epub 2007 May 25. Endocr J. 2007. PMID: 17527005 Free article.

8

A Japanese patient of congenital hypothyroidism with cerebellar atrophy.

Tajima T, Fujiwara F, Sudo A, Saito S, Fujieda K. Tajima T, et al. Endocr J. 2007 Dec;54(6):941-4. doi: 10.1507/endocrj.k07-105. Epub 2007 Nov 14. Endocr J. 2007. PMID: 18000345 Free article.

9

Four Japanese patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by DAX-1 gene mutations: mutant DAX-1 failed to repress steroidogenic acute regulatory protein (StAR) and luteinizing hormone beta-subunit gene promoter activity.

Okuhara K, Abe S, Kondo T, Fujita K, Koda N, Mochizuki H, Fujieda K, Tajima T. Okuhara K, et al. Among authors: tajima t. Endocr J. 2008 Mar;55(1):97-103. doi: 10.1507/endocrj.k07e-008. Epub 2008 Jan 17. Endocr J. 2008. PMID: 18202527 Free article.

10

Case study of a 15-year-old boy with McCune-Albright syndrome combined with pituitary gigantism: effect of octreotide-long acting release (LAR) and cabergoline therapy.

Tajima T, Tsubaki J, Ishizu K, Jo W, Ishi N, Fujieda K. Tajima T, et al. Endocr J. 2008 Jul;55(3):595-9. doi: 10.1507/endocrj.k07e-042. Epub 2008 Apr 30. Endocr J. 2008. PMID: 18445999 Free article.

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