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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 <i>NOD2</i> genetic mutationWoojoong Kim, Eujin Park, Yo Han Ahn, et al.Pediatric Nephrology (Berlin, Germany)|April 14, 2017
Focal segmental glomerulosclerosis and medullary nephrocalcinosis in children with ADCK4 mutationsEujin Park, Hee Gyung Kang, Young Hun Choi, 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|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.Pediatric Radiology|June 14, 2006
Nutcracker syndrome in children with gross haematuria: Doppler sonographic evaluation of the left renal veinJung-Eun Cheon, Woo Sun Kim, In-One Kim, 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.Annals of Clinical and Laboratory Science|October 31, 2018
Cutaneous Skeletal Hypophosphatemia Syndrome in Association with a Mosaic <i>HRAS</i> MutationPeong Gang Park, Eujin Park, Hye-Sun Hyun, et al.Journal of Korean Medical Science|November 17, 2020
Renal Syndromic Hearing Loss Is Common in Childhood-onset Chronic Kidney DiseaseJi Hyun Kim, Dong Han Lee, Bongjin Lee, et al.Pageof 20