Toyoura T - Search Results

1

Urinary pregnanetriol-3-glucuronide in children: age-related change and application to the management of 21-hydroxylase deficiency.

Yang Y, Saisho S, Toyoura T, Shimozawa K, Yata J. Yang Y, et al. Among authors: toyoura t. Acta Paediatr Jpn. 1996 Apr;38(2):107-13. doi: 10.1111/j.1442-200x.1996.tb03449.x. Acta Paediatr Jpn. 1996. PMID: 8677783

2

Genetic analysis of Japanese patients with 21-hydroxylase deficiency: identification of a patient with a new mutation of a homozygous deletion of adenine at codon 246 and patients without demonstrable mutations within the structural gene for CYP21.

Koyama S, Toyoura T, Saisho S, Shimozawa K, Yata J. Koyama S, et al. Among authors: toyoura t. J Clin Endocrinol Metab. 2002 Jun;87(6):2668-73. doi: 10.1210/jcem.87.6.8522. J Clin Endocrinol Metab. 2002. PMID: 12050231

3

Clinical course of patients with nonclassical 21-hydroxylase deficiency (21-OHD) diagnosed in infancy and childhood.

Kashimada K, Ono M, Onishi T, Koyama S, Toyoura T, Imai K, Saisho S, Mizutani S. Kashimada K, et al. Among authors: toyoura t. Endocr J. 2008 May;55(2):397-404. doi: 10.1507/endocrj.k07e-057. Epub 2008 Apr 2. Endocr J. 2008. PMID: 18385531 Free article.

4

[Results of genitoplasty for virilized genitalia of 41 females with congenital adrenal hyperplasia].

Kitahara S, Higashi Y, Tsujii T, Kageyama Y, Kawakami S, Toyoura T, Saisho S, Morita T, Takagi K, Oshima H. Kitahara S, et al. Among authors: toyoura t. Nihon Hinyokika Gakkai Zasshi. 1996 Dec;87(12):1289-96. doi: 10.5980/jpnjurol1989.87.1289. Nihon Hinyokika Gakkai Zasshi. 1996. PMID: 8997076 Free article. Japanese.

5

Molecular basis of nonclassical steroid 21-hydroxylase deficiency detected by neonatal mass screening in Japan.

Tajima T, Fujieda K, Nakae J, Toyoura T, Shimozawa K, Kusuda S, Goji K, Nagashima T, Cutler GB Jr. Tajima T, et al. Among authors: toyoura t. J Clin Endocrinol Metab. 1997 Jul;82(7):2350-6. doi: 10.1210/jcem.82.7.4094. J Clin Endocrinol Metab. 1997. PMID: 9215318

6

Elevated urine pregnanetriolone definitively establishes the diagnosis of classical 21-hydroxylase deficiency in term and preterm neonates.

Homma K, Hasegawa T, Takeshita E, Watanabe K, Anzo M, Toyoura T, Jinno K, Ohashi T, Hamajima T, Takahashi Y, Takahashi T, Matsuo N. Homma K, et al. Among authors: toyoura t. J Clin Endocrinol Metab. 2004 Dec;89(12):6087-91. doi: 10.1210/jc.2004-0473. J Clin Endocrinol Metab. 2004. PMID: 15579762

7

[Disturbance of active sleep components in neonates with congenital hypothyroidism].

Araki S, Toyoura T, Kohyama J, Shimohira M, Iwakawa Y. Araki S, et al. Among authors: toyoura t. No To Hattatsu. 1996 Nov;28(6):484-9. No To Hattatsu. 1996. PMID: 8940874 Japanese.

8

An XX male with microphthalmos and sclerocornea.

Kobayashi M, Kiyosawa M, Toyoura T, Tokoro T. Kobayashi M, et al. Among authors: toyoura t. J Pediatr Ophthalmol Strabismus. 1998 Mar-Apr;35(2):122-4. doi: 10.3928/0191-3913-19980301-15. J Pediatr Ophthalmol Strabismus. 1998. PMID: 9559515 No abstract available.

9

[A case of neonatal meningitis due to Flavobacterium meningosepticum successfully treated with cefmetazole and cefotaxime].

Takeda A, Toyoura T, Kiyohara K, Shimohira M, Arai S, Fukuda C. Takeda A, et al. Among authors: toyoura t. Jpn J Antibiot. 1988 May;41(5):557-62. Jpn J Antibiot. 1988. PMID: 3063849 Review. Japanese.

10

[Fundamental and clinical studies of cefaclor in oral surgery].

Morihana K, Sakamoto H, Gotoh J, Konnai T, Uematsu M, Toyoura T, Sasaki J, Ohno K, Yoshida H, Hasegawa M, et al. Morihana K, et al. Among authors: toyoura t. Jpn J Antibiot. 1984 Jun;37(6):1006-22. Jpn J Antibiot. 1984. PMID: 6387212 Japanese.

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