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Pediatric Transplantation|December 6, 2012
Leflunomide therapy for BK virus allograft nephropathy after pediatric kidney transplantationYoung H Jung, Kyung C Moon, Jong W Ha, et al.
Korean Journal of Pediatrics|April 30, 2014
Outcomes of chronic dialysis in Korean children with respect to survival rates and causes of deathHye Jin Chang, Kyoung Hee Han, Min Hyun Cho, et al.
Pediatric Nephrology (Berlin, Germany)|December 17, 2010
A case of systemic amyloidosis associated with cyclic neutropeniaHyunKyung Lee, Kyoung Hee Han, Yun Hye Jung, et al.
Pediatric Nephrology (Berlin, Germany)|May 25, 2005
Mutational analysis of idiopathic renal hypouricemia in KoreaHae Il Cheong, Ju Hyung Kang, Joo Hoon Lee, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 26, 2008
Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicismHyun Jin Choi, Beom Hee Lee, Hee Yeon Cho, et al.
Korean Journal of Pediatrics|December 27, 2016
A familial case of Blau syndrome caused by a novel NOD2 genetic mutationWoojoong Kim, Eujin Park, Yo Han Ahn, et al.
Experimental and Clinical Transplantation : Official Journal of the Middle East Society for Organ Transplantation|June 19, 2015
Different Recurrence Rates Between Pediatric and Adult Renal Transplant for Immunoglobulin A Nephropathy: Predictors of Posttransplant RecurrenceSanghyun Ahn, Sang-Il Min, Seung-Kee Min, et al.
Kidney International|October 14, 2005
Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aalpha chain geneHee Gyung Kang, Alison Bybee, Il Soo Ha, et al.
Korean Journal of Pediatrics|December 31, 2010
A case of Bartter syndrome type I with atypical presentationsEun Hye Lee, Ju Sun Heo, Hyun Kyung Lee, et al.
Korean Journal of Pediatrics|April 20, 2011
A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor geneSe Eun Lee, Yun Hye Jung, Kyoung Hee Han, et al.
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