Moon KC - Search Results

1

Consensus regarding diagnosis and management of atypical hemolytic uremic syndrome.

Lee H, Kang E, Kang HG, Kim YH, Kim JS, Kim HJ, Moon KC, Ban TH, Oh SW, Jo SK, Cho H, Choi BS, Hong J, Cheong HI, Oh D. Lee H, et al. Among authors: moon kc. Korean J Intern Med. 2020 Jan;35(1):25-40. doi: 10.3904/kjim.2019.388. Epub 2020 Jan 2. Korean J Intern Med. 2020. PMID: 31935318 Free PMC article. Review.

2

mRNA expression of intercellular adhesion molecule-1 and vascular cell adhesion molecule-1 in acute renal allograft rejection.

Park SY, Kim HW, Moon KC, Hong HK, Lee HS. Park SY, et al. Among authors: moon kc. Transplantation. 2000 Jun 27;69(12):2554-60. doi: 10.1097/00007890-200006270-00014. Transplantation. 2000. PMID: 10910276

3

Expression of intercellular adhesion molecule-1 and vascular cell adhesion molecule-1 in human crescentic glomerulonephritis.

Moon KC, Park SY, Kim HW, Hong HK, Lee HS. Moon KC, et al. Histopathology. 2002 Aug;41(2):158-65. doi: 10.1046/j.1365-2559.2002.01446.x. Histopathology. 2002. PMID: 12147094

4

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: moon kc. 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

5

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. Among authors: moon kc. Pediatr Nephrol. 2008 Sep;23(9):1555-8. doi: 10.1007/s00467-008-0847-5. Epub 2008 May 15. Pediatr Nephrol. 2008. PMID: 18481107

6

Two Korean infants with genetically confirmed congenital nephrotic syndrome of Finnish type.

Lee BH, Ahn YH, Choi HJ, Kang HK, Kim SD, Cho BS, Moon KC, Ha IS, Cheong HI, Choi Y. Lee BH, et al. Among authors: moon kc. J Korean Med Sci. 2009 Jan;24 Suppl(Suppl 1):S210-4. doi: 10.3346/jkms.2009.24.S1.S210. Epub 2009 Jan 28. J Korean Med Sci. 2009. PMID: 19194555 Free PMC article.

7

Variable renal phenotype in a family with an INF2 mutation.

Lee HK, Han KH, Jung YH, Kang HG, Moon KC, Ha IS, Choi Y, Cheong HI. Lee HK, et al. Among authors: moon kc. Pediatr Nephrol. 2011 Jan;26(1):73-6. doi: 10.1007/s00467-010-1644-5. Epub 2010 Aug 28. Pediatr Nephrol. 2011. PMID: 20803156

8

A case of systemic amyloidosis associated with cyclic neutropenia.

Lee H, Han KH, Jung YH, Kang HG, Moon KC, Ha IS, Choi Y, Cheong HI. Lee H, et al. Among authors: moon kc. Pediatr Nephrol. 2011 Apr;26(4):625-9. doi: 10.1007/s00467-010-1715-7. Epub 2010 Dec 15. Pediatr Nephrol. 2011. PMID: 21161286

9

Renal manifestations of patients with MYH9-related disorders.

Han KH, Lee H, Kang HG, Moon KC, Lee JH, Park YS, Ha IS, Ahn HS, Choi Y, Cheong HI. Han KH, et al. Among authors: moon kc. Pediatr Nephrol. 2011 Apr;26(4):549-55. doi: 10.1007/s00467-010-1735-3. Epub 2011 Jan 6. Pediatr Nephrol. 2011. PMID: 21210153

10

Successfully treated multicentric Castleman's disease with renal thrombotic microangiopathy using rituximab and corticosteroid.

Lee JP, Kim DK, Oh DY, Paik JH, Moon KC, Kim S, Kim YS. Lee JP, et al. Among authors: moon kc. Clin Nephrol. 2011 Feb;75(2):165-70. doi: 10.5414/cn106491. Clin Nephrol. 2011. PMID: 21255547

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

622 results

Search Page