Kang HG - Search Results

1

Diagnostic yield and clinical utility of whole exome sequencing using an automated variant prioritization system, EVIDENCE.

Seo GH, Kim T, Choi IH, Park JY, Lee J, Kim S, Won DG, Oh A, Lee Y, Choi J, Lee H, Kang HG, Cho HY, Cho MH, Kim YJ, Yoon YH, Eun BL, Desnick RJ, Keum C, Lee BH. Seo GH, et al. Among authors: kang hg. Clin Genet. 2020 Dec;98(6):562-570. doi: 10.1111/cge.13848. Epub 2020 Sep 17. Clin Genet. 2020. PMID: 32901917 Free PMC article.

2

Idiopathic membranous nephropathy in children.

Lee BH, Cho HY, Kang HG, Ha IS, Cheong HI, Moon KC, Lim IS, Choi Y. Lee BH, et al. Among authors: kang hg. Pediatr Nephrol. 2006 Nov;21(11):1707-15. doi: 10.1007/s00467-006-0246-8. Epub 2006 Sep 2. Pediatr Nephrol. 2006. PMID: 16951933

3

Primary focal segmental glomerular sclerosis in children: clinical course and prognosis.

Paik KH, Lee BH, Cho HY, Kang HG, Ha IS, Cheong HI, Jin DK, Moon KC, Choi Y. Paik KH, et al. Among authors: kang hg. Pediatr Nephrol. 2007 Mar;22(3):389-95. doi: 10.1007/s00467-006-0301-5. Epub 2006 Oct 21. Pediatr Nephrol. 2007. PMID: 17058050

4

Clinical outcomes of childhood lupus nephritis: a single center's experience.

Lee BS, Cho HY, Kim EJ, Kang HG, Ha IS, Cheong HI, Kim JG, Lee HS, Choi Y. Lee BS, et al. Among authors: kang hg. Pediatr Nephrol. 2007 Feb;22(2):222-31. doi: 10.1007/s00467-006-0286-0. Epub 2006 Nov 28. Pediatr Nephrol. 2007. PMID: 17131162

5

Hyporeninemic hypoaldosteronism in a child with chronic kidney disease--is this condition renoprotective?

Lee BH, Kang HG, Choi Y. Lee BH, et al. Among authors: kang hg. Pediatr Nephrol. 2009 Sep;24(9):1771-2. doi: 10.1007/s00467-009-1121-1. Epub 2009 Feb 3. Pediatr Nephrol. 2009. PMID: 19189133 No abstract available.

6

UTI in infancy: are voiding cystourethrography and prophylactic antibiotics necessary?

Kang HG, Lee BH, Choi Y. Kang HG, et al. Pediatr Nephrol. 2009 Aug;24(8):1599-601. doi: 10.1007/s00467-009-1131-z. Epub 2009 Feb 10. Pediatr Nephrol. 2009. PMID: 19205750 No abstract available.

7

Atypical hemolytic uremic syndrome associated with complement factor H autoantibodies and CFHR1/CFHR3 deficiency.

Lee BH, Kwak SH, Shin JI, Lee SH, Choi HJ, Kang HG, Ha IS, Lee JS, Dragon-Durey MA, Choi Y, Cheong HI. Lee BH, et al. Among authors: kang hg. Pediatr Res. 2009 Sep;66(3):336-40. doi: 10.1203/PDR.0b013e3181b1bd4a. Pediatr Res. 2009. PMID: 19531976

8

Decreased renal uptake of (99m)Tc-DMSA in patients with tubular proteinuria.

Lee BH, Lee SH, Choi HJ, Kang HG, Oh SW, Lee DS, Ha IS, Choi Y, Cheong HI. Lee BH, et al. Among authors: kang hg. Pediatr Nephrol. 2009 Nov;24(11):2211-6. doi: 10.1007/s00467-009-1238-2. Epub 2009 Jul 5. Pediatr Nephrol. 2009. PMID: 19579036

9

Polymorphisms of the MDR1 and MIF genes in children with nephrotic syndrome.

Choi HJ, Cho HY, Ro H, Lee SH, Han KH, Lee H, Kang HG, Ha IS, Choi Y, Cheong HI. Choi HJ, et al. Among authors: kang hg. Pediatr Nephrol. 2011 Nov;26(11):1981-8. doi: 10.1007/s00467-011-1903-0. Epub 2011 May 8. Pediatr Nephrol. 2011. PMID: 21553324

10

Genetic basis of Bartter syndrome in Korea.

Lee BH, Cho HY, Lee H, Han KH, Kang HG, Ha IS, Lee JH, Park YS, Shin JI, Lee DY, Kim SY, Choi Y, Cheong HI. Lee BH, et al. Among authors: kang hg. Nephrol Dial Transplant. 2012 Apr;27(4):1516-21. doi: 10.1093/ndt/gfr475. Epub 2011 Aug 23. Nephrol Dial Transplant. 2012. PMID: 21865213

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