Sato N - Search Results

1

Japanese familial patients with male-limited precocious puberty.

Shinagawa T, Katsumata N, Sato N, Horikawa R, Tanae A, Tanaka T. Shinagawa T, et al. Among authors: sato n. Endocr J. 2000 Dec;47(6):777-82. doi: 10.1507/endocrj.47.777. Endocr J. 2000. PMID: 11228053 Free article.

2

Homozygous loss of the cyclin-dependent kinase 4-inhibitor (p16) gene in human leukemias.

Ogawa S, Hirano N, Sato N, Takahashi T, Hangaishi A, Tanaka K, Kurokawa M, Tanaka T, Mitani K, Yazaki Y, et al. Ogawa S, et al. Among authors: sato n. Blood. 1994 Oct 15;84(8):2431-5. Blood. 1994. PMID: 7919362 Free article.

3

Genetic linkage analyses of Romano-Ward syndrome (RWS) in 13 Japanese families.

Tanaka T, Nakahara K, Kato N, Imai T, Yamazaki T, Tomita H, Shimokawa H, Matsuhashi H, Sato N, Matsui M, et al. Tanaka T, et al. Among authors: sato n. Hum Genet. 1994 Oct;94(4):380-4. doi: 10.1007/BF00201597. Hum Genet. 1994. PMID: 7927333

4

[A case of acute hepatitis (severe type) due to varicella-zoster virus with DIC].

Yuki T, Nakajima Y, Tanaka T, Adachi H, Yosizawa T, Ogiwara T, Kitami N, Sato N. Yuki T, et al. Among authors: sato n. Nihon Shokakibyo Gakkai Zasshi. 1998 Apr;95(4):333-6. Nihon Shokakibyo Gakkai Zasshi. 1998. PMID: 9591410 Japanese. No abstract available.

5

Are cerebrovascular factors involved in Alzheimer's disease?

Kudo T, Imaizumi K, Tanimukai H, Katayama T, Sato N, Nakamura Y, Tanaka T, Kashiwagi Y, Jinno Y, Tohyama M, Takeda M. Kudo T, et al. Among authors: sato n. Neurobiol Aging. 2000 Mar-Apr;21(2):215-24. doi: 10.1016/s0197-4580(00)00129-9. Neurobiol Aging. 2000. PMID: 10867206 Review.

6

Bone mineral density in Turner syndrome: relation to GH treatment and estrogen treatment.

Sato N, Nimura A, Horikawa R, Katumata N, Tanae A, Tanaka T. Sato N, et al. Endocr J. 2000 Mar;47 Suppl:S115-9. doi: 10.1507/endocrj.47.supplmarch_s115. Endocr J. 2000. PMID: 10890198 Free article.

7

Analysis of the FGFR3 gene in Japanese patients with achondroplasia and hypochondroplasia.

Katsumata N, Mikami S, Nagashima-Miyokawa A, Nimura A, Sato N, Horikawa R, Tanae A, Tanaka T. Katsumata N, et al. Among authors: sato n. Endocr J. 2000 Mar;47 Suppl:S121-4. doi: 10.1507/endocrj.47.supplmarch_s121. Endocr J. 2000. PMID: 10890199 Free article.

8

Genetic and endocrinological evaluations of three 46,XX patients with congenital lipoid adrenal hyperplasia previously reported as having presented spontaneous puberty.

Tanae A, Katsumata N, Sato N, Horikawa R, Tanaka T. Tanae A, et al. Among authors: sato n. Endocr J. 2000 Oct;47(5):629-34. doi: 10.1507/endocrj.47.629. Endocr J. 2000. PMID: 11200945 Free article.

9

New compound heterozygous mutation in the CYP17 gene in a 46,XY girl with 17 alpha-hydroxylase/17,20-lyase deficiency.

Katsumata N, Satoh M, Mikami A, Mikami S, Nagashima-Miyokawa A, Sato N, Yokoya S, Tanaka T. Katsumata N, et al. Among authors: sato n. Horm Res. 2001;55(3):141-6. doi: 10.1159/000049986. Horm Res. 2001. PMID: 11549876

10

A novel and de novo splice-donor site mutation in intron 3 of the GH-1 gene in a patient with isolated growth hormone deficiency.

Katsumata N, Matsuo S, Sato N, Tanaka T. Katsumata N, et al. Among authors: sato n. Growth Horm IGF Res. 2001 Dec;11(6):378-83. doi: 10.1054/ghir.2001.0251. Growth Horm IGF Res. 2001. PMID: 11914025

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