Showing results (151-160 of 198) with videos related to
Sort By:
Pageof 20
Stem Cell Research|June 25, 2023
Generation of a human induced pluripotent stem cell line from a patient with dent diseaseXianying Fang, Ji Hyun Kim, Sheng Cui, et al.European Journal of Human Genetics : EJHG|February 24, 2025
Genotype of PAX2-related disorders correlates with kidney and ocular manifestationsJi Hyun Kim, Yo Han Ahn, Yeonji Jang, et al.Pediatric Nephrology (Berlin, Germany)|February 9, 2012
Familial renal glucosuria: a clinicogenetic study of 23 additional casesHyunKyung Lee, Kyoung Hee Han, Hye Won Park, et al.Frontiers in Medicine|March 30, 2023
Long-term outcome of Bartter syndrome in 54 patients: A multicenter study in KoreaNaye Choi, Seong Heon Kim, Eun Hui Bae, et al.Pediatric Nephrology (Berlin, Germany)|June 11, 2014
Muscle involvement in Dent disease 2Eujin Park, Hyun Jin Choi, Jiwon M Lee, et al.Frontiers in Medicine|June 16, 2023
Corrigendum: Long-term outcome of Bartter syndrome in 54 patients: a multicenter study in KoreaNaye Choi, Seong Heon Kim, Eun Hui Bae, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 26, 2011
Genetic basis of Bartter syndrome in KoreaBeom Hee Lee, Hee Yeon Cho, HyunKyung Lee, et al.BMC Nephrology|December 10, 2020
Left-ventricular diastolic dysfunction in Korean children with chronic kidney disease: data from the KNOW-Ped CKD studyJeong Yeon Kim, Yeonhee Lee, Hee Gyung Kang, et al.Journal of Clinical Medicine|February 1, 2019
Anemia and Iron Deficiency in Children with Chronic Kidney Disease (CKD): Data from the Know-Ped CKD StudyKeum Hwa Lee, Eujin Park, Hyun Jin Choi, et al.BMC Nephrology|April 18, 2014
Hyperuricemia and deterioration of renal function in autosomal dominant polycystic kidney diseaseMiyeun Han, Hayne Cho Park, Hyunsuk Kim, et al.Pageof 20