Takamura N - Search Results

1

A mutational hot spot in the Prop-1 gene in Russian children with combined pituitary hormone deficiency.

Fofanova OV, Takamura N, Kinoshita E, Parks JS, Brown MR, Peterkova VA, Evgrafov OV, Goncharov NP, Bulatov AA, Dedov II, Yamashita S. Fofanova OV, et al. Among authors: takamura n. Pituitary. 1998 Apr;1(1):45-9. doi: 10.1023/a:1009918924945. Pituitary. 1998. PMID: 11081182

2

[Congenital erythropoietic porphyria].

Tanigawa K, Takamura N, Yamashita S. Tanigawa K, et al. Among authors: takamura n. Nihon Rinsho. 1995 Jun;53(6):1422-6. Nihon Rinsho. 1995. PMID: 7616657 Review. Japanese.

3

A novel point mutation in congenital erythropoietic porphyria in two members of Japanese family.

Tanigawa K, Bensidhoum M, Takamura N, Namba H, Yamashita S, de Verneuil H, Ged C. Tanigawa K, et al. Among authors: takamura n. Hum Genet. 1996 May;97(5):557-60. doi: 10.1007/BF02281859. Hum Genet. 1996. PMID: 8655129

4

Novel point mutation in the uroporphyrinogen III synthase gene causes congenital erythropoietic porphyria of a Japanese family.

Takamura N, Hombrados I, Tanigawa K, Namba H, Nagayama Y, de Verneuil H, Yamashita S. Takamura N, et al. Am J Med Genet. 1997 Jun 13;70(3):299-302. doi: 10.1002/(sici)1096-8628(19970613)70:3<299::aid-ajmg16>3.0.co;2-g. Am J Med Genet. 1997. PMID: 9188670

5

Rarity of PIT1 involvement in children from Russia with combined pituitary hormone deficiency.

Fofanova OV, Takamura N, Kinoshita E, Yoshimoto M, Tsuji Y, Peterkova VA, Evgrafov OV, Dedov II, Goncharov NP, Yamashita S. Fofanova OV, et al. Among authors: takamura n. Am J Med Genet. 1998 Jun 5;77(5):360-5. doi: 10.1002/(sici)1096-8628(19980605)77:5<360::aid-ajmg4>3.0.co;2-r. Am J Med Genet. 1998. PMID: 9632165 Review.

6

Compound heterozygous deletion of the PROP-1 gene in children with combined pituitary hormone deficiency.

Fofanova O, Takamura N, Kinoshita E, Parks JS, Brown MR, Peterkova VA, Evgrafov OV, Goncharov NP, Bulatov AA, Dedov II, Yamashita S. Fofanova O, et al. Among authors: takamura n. J Clin Endocrinol Metab. 1998 Jul;83(7):2601-4. doi: 10.1210/jcem.83.7.5094. J Clin Endocrinol Metab. 1998. PMID: 9661653 Clinical Trial.

7

A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia.

Fofanova OV, Takamura N, Kinoshita E, Meerson EM, Iljina VK, Nechvolodova OL, Evgrafov OV, Peterkova VA, Yamashita S. Fofanova OV, et al. Among authors: takamura n. Endocr J. 1998 Dec;45(6):791-5. doi: 10.1507/endocrj.45.791. Endocr J. 1998. PMID: 10395236 Free article.

8

Prop-1 gene expression in human pituitary tumors.

Nakamura S, Ohtsuru A, Takamura N, Kitange G, Tokunaga Y, Yasunaga A, Shibata S, Yamashita S. Nakamura S, et al. Among authors: takamura n. J Clin Endocrinol Metab. 1999 Jul;84(7):2581-4. doi: 10.1210/jcem.84.7.5974. J Clin Endocrinol Metab. 1999. PMID: 10404841

9

[Genes for autoantigens].

Takamura N, Yamashita S. Takamura N, et al. Nihon Rinsho. 1999 Aug;57(8):1729-36. Nihon Rinsho. 1999. PMID: 10483241 Review. Japanese.

10

Gene analysis of PROP1 in dwarfism with combined pituitary hormone deficiency.

Takamura N, Fofanova OV, Kinoshita E, Yamashita S. Takamura N, et al. Growth Horm IGF Res. 1999 Jun;9 Suppl B:12-7. doi: 10.1016/s1096-6374(99)80075-6. Growth Horm IGF Res. 1999. PMID: 10549300

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