Yoo HW - Search Results

1

Cardiovascular anomalies in patients with chromosome 22q11.2 deletion: a Korean multicenter study.

Park IS, Ko JK, Kim YH, Yoo HW, Seo EJ, Choi JY, Gil HY, Kim SJ. Park IS, et al. Among authors: yoo hw. Int J Cardiol. 2007 Jan 8;114(2):230-5. doi: 10.1016/j.ijcard.2005.12.029. Epub 2006 Jul 7. Int J Cardiol. 2007. PMID: 16824627

2

Identification of a novel mutation in the GLUT2 gene in a patient with Fanconi-Bickel syndrome presenting with neonatal diabetes mellitus and galactosaemia.

Yoo HW, Shin YL, Seo EJ, Kim GH. Yoo HW, et al. Eur J Pediatr. 2002 Jun;161(6):351-3. doi: 10.1007/s00431-002-0931-y. Epub 2002 Apr 16. Eur J Pediatr. 2002. PMID: 12029458

3

Endocrine manifestations of chromosome 22q11.2 microdeletion syndrome.

Choi JH, Shin YL, Kim GH, Seo EJ, Kim Y, Park IS, Yoo HW. Choi JH, et al. Among authors: yoo hw. Horm Res. 2005;63(6):294-9. doi: 10.1159/000086745. Epub 2005 Jul 1. Horm Res. 2005. PMID: 15995343

4

Novel mutations in the human elastin gene (ELN) causing isolated supravalvular aortic stenosis.

Park S, Seo EJ, Yoo HW, Kim Y. Park S, et al. Among authors: yoo hw. Int J Mol Med. 2006 Aug;18(2):329-32. Int J Mol Med. 2006. PMID: 16820942

5

The IL-10 (-627 A/C) promoter polymorphism may be associated with coronary aneurysms and low serum albumin in Korean children with Kawasaki disease.

Jin HS, Kim HB, Kim BS, Lee JK, Seo EJ, Yoo HW, Park IS, Hong YM, Hong SJ. Jin HS, et al. Among authors: yoo hw. Pediatr Res. 2007 May;61(5 Pt 1):584-7. doi: 10.1203/pdr.0b013e3180459fb5. Pediatr Res. 2007. PMID: 17413867

6

The CCR5 (-2135C/T) polymorphism may be associated with the development of Kawasaki disease in Korean children.

Jhang WK, Kang MJ, Jin HS, Yu J, Kim BJ, Kim BS, Lee JK, Seo EJ, Yoo HW, Park IS, Hong YM, Hong SJ. Jhang WK, et al. Among authors: yoo hw. J Clin Immunol. 2009 Jan;29(1):22-8. doi: 10.1007/s10875-008-9218-z. Epub 2008 Jul 15. J Clin Immunol. 2009. PMID: 18629619

7

Molecular analysis of the AR and SRD5A2 genes in patients with 46,XY disorders of sex development.

Choi JH, Kim GH, Seo EJ, Kim KS, Kim SH, Yoo HW. Choi JH, et al. Among authors: yoo hw. J Pediatr Endocrinol Metab. 2008 Jun;21(6):545-53. J Pediatr Endocrinol Metab. 2008. PMID: 18717241

8

Genetic variants in the HLA-G region are associated with Kawasaki disease.

Kim JJ, Hong SJ, Hong YM, Kim S, Kang MJ, Kim KJ, Seo EJ, Yoo HW, Cheong HS, Shin HD, Park IS, Lee JK. Kim JJ, et al. Among authors: yoo hw. Hum Immunol. 2008 Dec;69(12):867-71. doi: 10.1016/j.humimm.2008.10.002. Epub 2008 Oct 29. Hum Immunol. 2008. PMID: 18976687

9

[Identification of a novel deletion region in 3q29 microdeletion syndrome by oligonucleotide array comparative genomic hybridization].

Seo EJ, Jun KR, Yoo HW, Yoo HK, Lee JO. Seo EJ, et al. Among authors: yoo hk, yoo hw. Korean J Lab Med. 2010 Feb;30(1):70-5. doi: 10.3343/kjlm.2010.30.1.70. Korean J Lab Med. 2010. PMID: 20197726 Korean.

10

Clinical and functional characteristics of a novel heterozygous mutation of the IGF1R gene and IGF1R haploinsufficiency due to terminal 15q26.2->qter deletion in patients with intrauterine growth retardation and postnatal catch-up growth failure.

Choi JH, Kang M, Kim GH, Hong M, Jin HY, Lee BH, Park JY, Lee SM, Seo EJ, Yoo HW. Choi JH, et al. Among authors: yoo hw. J Clin Endocrinol Metab. 2011 Jan;96(1):E130-4. doi: 10.1210/jc.2010-1789. Epub 2010 Oct 20. J Clin Endocrinol Metab. 2011. PMID: 20962017

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