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Pediatric Nephrology (Berlin, Germany)|May 13, 2004
Age-related differences in adriamycin-induced nephropathyHyewon Hahn, Young Seo Park, Il Soo Ha, et al.Journal of Korean Medical Science|March 25, 2018
Primary Autosomal Recessive Distal Renal Tubular Acidosis Caused by a Common Homozygous SLC4A1 Mutation in Two Lao FamiliesEujin Park, Vilaphone Phaymany, Eun Sang Yi, et al.Journal of Korean Medical Science|February 16, 2006
Two cases of isolated diffuse mesangial sclerosis with WT1 mutationsHyewon Hahn, Young Mi Cho, Young Seo Park, et al.Nephrology (Carlton, Vic.)|March 21, 2007
Molecular genetic study of congenital nephrogenic diabetes insipidus and rescue of mutant vasopressin V2 receptor by chemical chaperonesHae Il Cheong, Hee Yeon Cho, Hye Won Park, et al.Pediatric Nephrology (Berlin, Germany)|November 17, 2006
Pattern of double glomerulopathy in childrenHae Il Cheong, Hee Yeon Cho, Kyung Chul Moon, et al.Annals of Pediatric Endocrinology & Metabolism|June 7, 2014
Gitelman syndrome combined with complete growth hormone deficiencySe Ra Min, Hyun Seok Cho, Jeana Hong, et al.Yonsei Medical Journal|April 14, 2011
ADAMTS13 gene mutations in children with hemolytic uremic syndromeHyoung Soo Choi, Hae Il Cheong, Nam Keun Kim, et al.Endocrine Journal|November 4, 2021
Burden of disease of X-linked hypophosphatemia in Japanese and Korean patients: a cross-sectional surveyNobuaki Ito, Hee Gyung Kang, Yayoi Nishida, et al.Journal of Pediatric Ophthalmology and Strabismus|August 4, 2009
Presumed atypical HDR syndrome associated with Band Keratopathy and pigmentary retinopathyCinoo Kim, Hae Il Cheong, Jeong Hun Kim, et al.Journal of Korean Medical Science|January 16, 2016
Mutations in SLC12A3 and CLCNKB and Their Correlation with Clinical Phenotype in Patients with Gitelman and Gitelman-like SyndromeJae Wook Lee, Jeonghwan Lee, Nam Ju Heo, et al.Pageof 20