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Annals of Clinical and Laboratory Science|February 20, 2015
A novel NOTCH2 mutation identified in a Korean family with Hajdu-Cheney syndrome showing phenotypic diversityMi Seon Han, Jung Min Ko, Tae-Joon Cho, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 19, 2016
NUP107 mutations in children with steroid-resistant nephrotic syndromeEujin Park, Yo Han Ahn, Hee Gyung Kang, et al.The Journal of Pediatrics|June 30, 2009
Dent-2 disease: a mild variant of Lowe syndromeArend Bökenkamp, Detlef Böckenhauer, Hae Il Cheong, et al.Korean Journal of Pediatrics|December 27, 2016
A nonsense <i>PAX6</i> mutation in a family with congenital aniridiaKyoung Hee Han, Hye Jin Lee, Il-Soo Ha, et al.Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|December 5, 2012
Prevalence of 25(OH) vitamin D insufficiency and deficiency in pediatric patients on chronic dialysisHee Yeon Cho, Hye Sun Hyun, Hee Gyung Kang, et al.Kidney Research and Clinical Practice|January 9, 2019
Disseminated adenovirus infection in a 10-year-old renal allograft recipientBora Lee, Eujin Park, Jongwon Ha, et al.Frontiers in Pediatrics|August 26, 2021
Genotype and Phenotype Analysis in X-Linked HypophosphatemiaPeong Gang Park, Seon Hee Lim, HyunKyung Lee, et al.Pediatric Nephrology (Berlin, Germany)|November 15, 2011
Urinary exosomal WT1 in childhood nephrotic syndromeHyunkyung Lee, Kyoung Hee Han, Se Eun Lee, et al.Journal of Korean Medical Science|December 20, 2005
Two novel mutations in the aquaporin 2 gene in a girl with congenital nephrogenic diabetes insipidusHae Il Cheong, Su Jin Cho, Shou Huan Zheng, et al.Pediatric Nephrology (Berlin, Germany)|February 14, 2007
Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonateHee Yeon Cho, Byong Sop Lee, Kyung Chul Moon, et al.Pageof 20