Cheong HI - Search Results

1

Reduced urinary excretion of thiazide-sensitive Na-Cl cotransporter in Gitelman syndrome: preliminary data.

Joo KW, Lee JW, Jang HR, Heo NJ, Jeon US, Oh YK, Lim CS, Na KY, Kim J, Cheong HI, Han JS. Joo KW, et al. Among authors: cheong hi. Am J Kidney Dis. 2007 Nov;50(5):765-73. doi: 10.1053/j.ajkd.2007.07.022. Am J Kidney Dis. 2007. PMID: 17954289

2

ATP6B1 gene mutations associated with distal renal tubular acidosis and deafness in a child.

Hahn H, Kang HG, Ha IS, Cheong HI, Choi Y. Hahn H, et al. Among authors: cheong hi. Am J Kidney Dis. 2003 Jan;41(1):238-43. doi: 10.1053/ajkd.2003.50014. Am J Kidney Dis. 2003. PMID: 12500243

3

Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicism.

Choi HJ, Lee BH, Cho HY, Moon KC, Ha IS, Nagata M, Choi Y, Cheong HI. Choi HJ, et al. Among authors: cheong hi. Am J Kidney Dis. 2008 May;51(5):834-8. doi: 10.1053/j.ajkd.2008.01.018. Am J Kidney Dis. 2008. PMID: 18436095

4

A case of hemolytic uremic syndrome preceded by intussusception.

Ko EY, Kim JY, Lee HJ, Lee HS, Han JW, Kim YH, Kim JT, Cheong HI, Jang PS. Ko EY, et al. Among authors: cheong hi. Korean J Pediatr. 2011 Apr;54(4):176-8. doi: 10.3345/kjp.2011.54.4.176. Epub 2011 Apr 30. Korean J Pediatr. 2011. PMID: 21738552 Free PMC article.

5

Urinary N-acetyl-β-D glucosaminidase as a surrogate marker for renal function in autosomal dominant polycystic kidney disease: 1 year prospective cohort study.

Park HC, Hwang JH, Kang AY, Ro H, Kim MG, An JN, In Park J, Kim SH, Yang J, Oh YK, Oh KH, Noh JW, Cheong HI, Hwang YH, Ahn C. Park HC, et al. Among authors: cheong hi. BMC Nephrol. 2012 Aug 30;13:93. doi: 10.1186/1471-2369-13-93. BMC Nephrol. 2012. PMID: 22935351 Free PMC article.

6

Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like Syndrome.

Lee JW, Lee J, Heo NJ, Cheong HI, Han JS. Lee JW, et al. Among authors: cheong hi. J Korean Med Sci. 2016 Jan;31(1):47-54. doi: 10.3346/jkms.2016.31.1.47. Epub 2015 Dec 24. J Korean Med Sci. 2016. PMID: 26770037 Free PMC article.

7

Glucocorticoid diminishes vascular endothelial growth factor and exacerbates proteinuria in rats with mesangial proliferative glomerulonephritis.

Ha IS, Um EY, Jung HR, Park HW, Cheong HI, Choi Y. Ha IS, et al. Among authors: cheong hi. Am J Kidney Dis. 2002 May;39(5):1001-10. doi: 10.1053/ajkd.2002.32773. Am J Kidney Dis. 2002. PMID: 11979343

8

Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aalpha chain gene.

Kang HG, Bybee A, Ha IS, Park MS, Gilbertson JA, Cheong HI, Choi Y, Hawkins PN. Kang HG, et al. Among authors: cheong hi. Kidney Int. 2005 Nov;68(5):1994-8. doi: 10.1111/j.1523-1755.2005.00653.x. Kidney Int. 2005. PMID: 16221199 Free article.

9

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: cheong hi. Nephrol Dial Transplant. 2012 Apr;27(4):1516-21. doi: 10.1093/ndt/gfr475. Epub 2011 Aug 23. Nephrol Dial Transplant. 2012. PMID: 21865213

10

Urinary exosomal WT1 in childhood nephrotic syndrome.

Lee H, Han KH, Lee SE, Kim SH, Kang HG, Cheong HI. Lee H, et al. Among authors: cheong hi. Pediatr Nephrol. 2012 Feb;27(2):317-20. doi: 10.1007/s00467-011-2035-2. Epub 2011 Nov 11. Pediatr Nephrol. 2012. PMID: 22076591

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