Shinagawa T - Search Results

1

A novel frameshift mutation 840delA and a novel polymorphism D203A in the steroidogenic acute regulatory protein gene in a Japanese patient with congenital lipoid adrenal hyperplasia. Mutations in brief no. 117. Online.

Katsumata N, Tanae A, Shinagawa T, Nagashima-Miyokawa A, Shimizu M, Yasunaga T, Tanaka T, Hibi I. Katsumata N, et al. Among authors: shinagawa t. Hum Mutat. 1998;11(4):331. doi: 10.1002/(SICI)1098-1004(1998)11:4<331::AID-HUMU12>3.0.CO;2-3. Hum Mutat. 1998. PMID: 10215405

2

Homozygous Q258X mutation in the steroidogenic acute regulatory gene in a Japanese patient with congenital lipoid adrenal hyperplasia.

Katsumata N, Tanae A, Shinagawa T, Nagashima-Miyokawa A, Shimizu M, Yasunaga T, Tanaka T, Hibi I. Katsumata N, et al. Among authors: shinagawa t. Endocr J. 1997 Jun;44(3):441-6. doi: 10.1507/endocrj.44.441. Endocr J. 1997. PMID: 9279522 Free article.

3

Novel frameshift mutation 840delA and a novel polymorphism D203A in the steroidogenic acute regulatory protein gene in a Japanese patient with congenital lipoid adrenal hyperplasia.

Katsumata N, Tanae A, Shinagawa T, Nagashima-Miyokawa A, Shimizu M, Yasunaga T, Tanaka T, Hibi I. Katsumata N, et al. Among authors: shinagawa t. Hum Mutat. 1998;Suppl 1:S304-7. doi: 10.1002/humu.1380110195. Hum Mutat. 1998. PMID: 9452116 No abstract available.

4

Nonclassic steroid 21-hydroxylase deficiency due to a homozygous V281L mutation in CYP21A2 detected by the neonatal mass-screening program in Japan.

Shinagawa T, Horikawa R, Isojima T, Naiki Y, Tanaka T, Katsumata N. Shinagawa T, et al. Endocr J. 2007 Dec;54(6):1021-5. doi: 10.1507/endocrj.k07-028. Epub 2007 Nov 30. Endocr J. 2007. PMID: 18048990 Free article.

5

Novel intronic CYP21A2 mutation in a Japanese patient with classic salt-wasting steroid 21-hydroxylase deficiency.

Katsumata N, Shinagawa T, Horikawa R, Fujikura K. Katsumata N, et al. Among authors: shinagawa t. Metabolism. 2010 Nov;59(11):1628-32. doi: 10.1016/j.metabol.2010.03.012. Epub 2010 Apr 27. Metabolism. 2010. PMID: 20423741

6

Mechanism for the development of ovarian cysts in patients with congenital lipoid adrenal hyperplasia.

Shima M, Tanae A, Miki K, Katsumata N, Matsumoto S, Nakajima S, Harada T, Shinagawa T, Tanaka T, Okada S. Shima M, et al. Among authors: shinagawa t. Eur J Endocrinol. 2000 Mar;142(3):274-9. doi: 10.1530/eje.0.1420274. Eur J Endocrinol. 2000. PMID: 10700722

7

Japanese familial patients with male-limited precocious puberty.

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

8

False negatives at neonatal screening for congenital adrenal hyperplasia in two siblings with 21-hydroxylase deficiency.

Shinohara O, Ishiguro H, Shinagawa T, Kubota C. Shinohara O, et al. Among authors: shinagawa t. Endocr J. 1998 Jun;45(3):427-30. doi: 10.1507/endocrj.45.427. Endocr J. 1998. PMID: 9790280 Free article.

9

Spontaneous reduction of a recurrent craniopharyngioma in an 8-year-old female patient: case report.

Shinohara O, Shinagawa T, Kubota C, Oi S. Shinohara O, et al. Among authors: shinagawa t. Neurosurgery. 1997 Nov;41(5):1188-90. doi: 10.1097/00006123-199711000-00033. Neurosurgery. 1997. PMID: 9361075

10

Moyamoya disease complicated with renal artery stenosis and nephrotic syndrome: reversal of nephrotic syndrome after nephrectomy.

Kuwayama F, Hamasaki Y, Shinagawa T, Kubota C, Ichikawa I, Kato Y, Oi S, Shinohara O. Kuwayama F, et al. Among authors: shinagawa t. J Pediatr. 2001 Mar;138(3):418-20. doi: 10.1067/mpd.2001.111330. J Pediatr. 2001. PMID: 11241054

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