Kawashima Y - Search Results

1

Variation analysis of beta3-adrenergic receptor and melanocortin-4 receptor genes in childhood obesity.

Kinoshita T, Hanaki K, Nagaishi J, Kawashima Y, Adachi K, Nanba E, Kanzaki S. Kinoshita T, et al. Among authors: kawashima y. Pediatr Int. 2007 Apr;49(2):133-7. doi: 10.1111/j.1442-200X.2007.02334.x. Pediatr Int. 2007. PMID: 17445027

2

Mutation at cleavage site of insulin-like growth factor receptor in a short-stature child born with intrauterine growth retardation.

Kawashima Y, Kanzaki S, Yang F, Kinoshita T, Hanaki K, Nagaishi J, Ohtsuka Y, Hisatome I, Ninomoya H, Nanba E, Fukushima T, Takahashi S. Kawashima Y, et al. J Clin Endocrinol Metab. 2005 Aug;90(8):4679-87. doi: 10.1210/jc.2004-1947. Epub 2005 May 31. J Clin Endocrinol Metab. 2005. PMID: 15928254

3

Late-onset adrenal hypoplasia congenita caused by a novel mutation of the DAX-1 gene.

Yang F, Hanaki K, Kinoshita T, Kawashima Y, Nagaishi J, Kanzaki S. Yang F, et al. Among authors: kawashima y. Eur J Pediatr. 2009 Mar;168(3):329-31. doi: 10.1007/s00431-008-0779-x. Epub 2008 Jul 8. Eur J Pediatr. 2009. PMID: 18607630

4

Familial short stature with IGF-I receptor gene anomaly.

Kawashima Y, Takahashi S, Kanzaki S. Kawashima Y, et al. Endocr J. 2012;59(3):179-85. doi: 10.1507/endocrj.ej11-0258. Epub 2011 Oct 19. Endocr J. 2012. PMID: 22008389 Free article. Review.

5

Novel missense mutation in the IGF-I receptor L2 domain results in intrauterine and postnatal growth retardation.

Kawashima Y, Higaki K, Fukushima T, Hakuno F, Nagaishi J, Hanaki K, Nanba E, Takahashi S, Kanzaki S. Kawashima Y, et al. Clin Endocrinol (Oxf). 2012 Aug;77(2):246-54. doi: 10.1111/j.1365-2265.2012.04357.x. Clin Endocrinol (Oxf). 2012. PMID: 22309212

6

Pericentric inversion inv(2) (p11.2q21) associated with Treacher Collins-Franceschetti syndrome.

Sawada H, Kawashima Y, Yamamoto Y, Egi T, Nagata I, Kanzaki S. Sawada H, et al. Among authors: kawashima y. Pediatr Int. 2002 Jun;44(3):328-9. doi: 10.1046/j.1442-200x.2002.01546.x. Pediatr Int. 2002. PMID: 11982909 No abstract available.

7

Aplastic anemia during growth hormone (GH) treatment in a girl with idiopathic GH-deficiency.

Sugimoto S, Hanaki K, Kawashima Y, Kinoshita T, Nagaishi J, Hayashi A, Kanzaki S. Sugimoto S, et al. Among authors: kawashima y. Endocr J. 2003 Aug;50(4):469-71. doi: 10.1507/endocrj.50.469. Endocr J. 2003. PMID: 14599122 Free article.

8

Leprechaunism (Donohue syndrome): a case bearing novel compound heterozygous mutations in the insulin receptor gene.

Kawashima Y, Nishimura R, Utsunomiya A, Kagawa R, Funata H, Fujimoto M, Hanaki K, Kanzaki S. Kawashima Y, et al. Endocr J. 2013;60(1):107-12. doi: 10.1507/endocrj.ej12-0289. Epub 2012 Oct 9. Endocr J. 2013. PMID: 22972224 Free article.

9

Familial short stature is associated with a novel dominant-negative heterozygous insulin-like growth factor 1 receptor (IGF1R) mutation.

Kawashima Y, Hakuno F, Okada S, Hotsubo T, Kinoshita T, Fujimoto M, Nishimura R, Fukushima T, Hanaki K, Takahashi S, Kanzaki S. Kawashima Y, et al. Clin Endocrinol (Oxf). 2014 Aug;81(2):312-4. doi: 10.1111/cen.12317. Epub 2013 Sep 30. Clin Endocrinol (Oxf). 2014. PMID: 24033502 No abstract available.

10

Clinical overview of nephrogenic diabetes insipidus based on a nationwide survey in Japan.

Fujimoto M, Okada S, Kawashima Y, Nishimura R, Miyahara N, Kawaba Y, Hanaki K, Nanba E, Kondo Y, Igarashi T, Kanzaki S. Fujimoto M, et al. Among authors: kawashima y. Yonago Acta Med. 2014 Jun;57(2):85-91. Epub 2014 Jul 30. Yonago Acta Med. 2014. PMID: 25324589 Free PMC article.

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