Koda N - Search Results

1

Structure of the human glucokinase gene and identification of a missense mutation in a Japanese patient with early-onset non-insulin-dependent diabetes mellitus.

Sakura H, Eto K, Kadowaki H, Simokawa K, Ueno H, Koda N, Fukushima Y, Akanuma Y, Yazaki Y, Kadowaki T. Sakura H, et al. Among authors: koda n. J Clin Endocrinol Metab. 1992 Dec;75(6):1571-3. doi: 10.1210/jcem.75.6.1464666. J Clin Endocrinol Metab. 1992. PMID: 1464666

2

Four mutant alleles of the insulin receptor gene associated with genetic syndromes of extreme insulin resistance.

Kadowaki H, Takahashi Y, Ando A, Momomura K, Kaburagi Y, Quin JD, MacCuish AC, Koda N, Fukushima Y, Taylor SI, Akanuma Y, Yazaki Y, Kadowaki T. Kadowaki H, et al. Among authors: koda n. Biochem Biophys Res Commun. 1997 Aug 28;237(3):516-20. doi: 10.1006/bbrc.1997.7181. Biochem Biophys Res Commun. 1997. PMID: 9299395

3

A Japanese case of congenital hyperinsulinism with hyperammonemia due to a mutation in glutamate dehydrogenase (GLUD1) gene.

Yasuda K, Koda N, Kadowaki H, Ogawa Y, Kimura S, Kadowaki T, Akanuma Y. Yasuda K, et al. Among authors: koda n. Intern Med. 2001 Jan;40(1):32-7. doi: 10.2169/internalmedicine.40.32. Intern Med. 2001. PMID: 11201367 Free article.

4

Analysis of the steroidogenic acute regulatory protein (StAR) gene in Japanese patients with congenital lipoid adrenal hyperplasia.

Nakae J, Tajima T, Sugawara T, Arakane F, Hanaki K, Hotsubo T, Igarashi N, Igarashi Y, Ishii T, Koda N, Kondo T, Kohno H, Nakagawa Y, Tachibana K, Takeshima Y, Tsubouchi K, Strauss JF 3rd, Fujieda K. Nakae J, et al. Among authors: koda n. Hum Mol Genet. 1997 Apr;6(4):571-6. doi: 10.1093/hmg/6.4.571. Hum Mol Genet. 1997. PMID: 9097960

5

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: koda n. 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.

6

Severe hypercalcaemia and respiratory insufficiency associated with infantile hypophosphatasia caused by two novel mutations of the tissue-nonspecific alkaline phosphatase gene.

Mochizuki H, Saito M, Michigami T, Ohashi H, Koda N, Yamaguchi S, Ozono K. Mochizuki H, et al. Among authors: koda n. Eur J Pediatr. 2000 May;159(5):375-9. doi: 10.1007/s004310051290. Eur J Pediatr. 2000. PMID: 10834525

7

Accurate localization of an insulinoma by preoperative selective intra-arterial calcium injection and intraoperative glucose monitoring.

Iwanaka T, Matsumoto M, Yoshikawa Y, Koda N, Mochizuki H, Aihara T, Imaizumi S. Iwanaka T, et al. Among authors: koda n. Pediatr Surg Int. 2000;16(1-2):118-20. doi: 10.1007/s003830050036. Pediatr Surg Int. 2000. PMID: 10663858

8

The association of hypopituitarism with small pituitary, invisible pituitary stalk, type 1 Arnold-Chiari malformation, and syringomyelia in seven patients born in breech position: a further proof of birth injury theory on the pathogenesis of "idiopathic hypopituitarism".

Fujita K, Matsuo N, Mori O, Koda N, Mukai E, Okabe Y, Shirakawa N, Tamai S, Itagane Y, Hibi I. Fujita K, et al. Among authors: koda n. Eur J Pediatr. 1992 Apr;151(4):266-70. doi: 10.1007/BF02072226. Eur J Pediatr. 1992. PMID: 1499578

9

Quick screening and diagnosis of organic acidemia by NMR urinalysis.

Yamaguchi S, Koda N, Eto Y, Aoki K. Yamaguchi S, et al. Among authors: koda n. J Pediatr. 1985 Apr;106(4):620-2. doi: 10.1016/s0022-3476(85)80088-3. J Pediatr. 1985. PMID: 3981318 No abstract available.

10

Rapid chemical diagnosis of kerosene ingestion by NMR.

Yamaguchi S, Yamamoto H, Mizukoshi R, Koda N, Hamano S, Nozaki H, Fujiwara M. Yamaguchi S, et al. Among authors: koda n. Clin Chem. 1992 Apr;38(4):593. Clin Chem. 1992. PMID: 1568331 No abstract available.

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