Park HW - Search Results

1

Molecular genetic study of congenital nephrogenic diabetes insipidus and rescue of mutant vasopressin V2 receptor by chemical chaperones.

Cheong HI, Cho HY, Park HW, Ha IS, Choi Y. Cheong HI, et al. Among authors: park hw. Nephrology (Carlton). 2007 Apr;12(2):113-7. doi: 10.1111/j.1440-1797.2006.00759.x. Nephrology (Carlton). 2007. PMID: 17371330

2

Six novel mutations in the vasopressin V2 receptor gene causing nephrogenic diabetes insipidus.

Cheong HI, Park HW, Ha IS, Moon HN, Choi Y, Ko KW, Jun JK. Cheong HI, et al. Among authors: park hw. Nephron. 1997;75(4):431-7. doi: 10.1159/000189581. Nephron. 1997. PMID: 9127330

3

Circulating VEGF and TGF-beta1 in children with idiopathic nephrotic syndrome.

Cheong HI, Lee JH, Hahn H, Park HW, Ha IS, Choi Y. Cheong HI, et al. Among authors: park hw. J Nephrol. 2001 Jul-Aug;14(4):263-9. J Nephrol. 2001. PMID: 11506248

4

Mutational analysis of COL4A5 gene in Korean Alport syndrome.

Cheong HI, Park HW, Ha IS, Choi Y. Cheong HI, et al. Among authors: park hw. Pediatr Nephrol. 2000 Feb;14(2):117-21. doi: 10.1007/s004670050025. Pediatr Nephrol. 2000. PMID: 10684360 Clinical Trial.

5

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: park hw. Am J Kidney Dis. 2002 May;39(5):1001-10. doi: 10.1053/ajkd.2002.32773. Am J Kidney Dis. 2002. PMID: 11979343

6

Congenital thrombotic thrombocytopenic purpura associated with unilateral moyamoya disease.

Park HW, Oh D, Kim N, Cho HY, Moon KC, Chae JH, Ahn HS, Choi Y, Cheong HI. Park HW, et al. Pediatr Nephrol. 2008 Sep;23(9):1555-8. doi: 10.1007/s00467-008-0847-5. Epub 2008 May 15. Pediatr Nephrol. 2008. PMID: 18481107

7

ADAMTS13 gene mutations in children with hemolytic uremic syndrome.

Choi HS, Cheong HI, Kim NK, Oh D, Park HW. Choi HS, et al. Among authors: park hw. Yonsei Med J. 2011 May;52(3):530-4. doi: 10.3349/ymj.2011.52.3.530. Yonsei Med J. 2011. PMID: 21488199 Free PMC article.

8

Hypokalemic periodic paralysis; two different genes responsible for similar clinical manifestations.

Kim H, Hwang H, Cheong HI, Park HW. Kim H, et al. Among authors: park hw. Korean J Pediatr. 2011 Nov;54(11):473-6. doi: 10.3345/kjp.2011.54.11.473. Epub 2011 Nov 30. Korean J Pediatr. 2011. PMID: 22253645 Free PMC article.

9

Hereditary glomerulopathy associated with a mitochondrial tRNA(Leu) gene mutation.

Cheong HI, Chae JH, Kim JS, Park HW, Ha IS, Hwang YS, Lee HS, Choi Y. Cheong HI, et al. Among authors: park hw. Pediatr Nephrol. 1999 Aug;13(6):477-80. doi: 10.1007/s004670050641. Pediatr Nephrol. 1999. PMID: 10452273

10

Association of angiotensin I converting enzyme gene polymorphism with reflux nephropathy in children.

Park HW, Koo JW, Kim JS, Ha IS, Cheong HI, Choi Y. Park HW, et al. Nephron. 2000 Sep;86(1):52-5. doi: 10.1159/000045712. Nephron. 2000. PMID: 10971153 Clinical Trial.

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