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Journal of Clinical Medicine|March 14, 2020
Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary TractYo Han Ahn, Chung Lee, Nayoung K D Kim, et al.
Pediatric Transplantation|September 11, 2023
Clinical course of post-kidney transplant Schimke immuno-osseous dysplasiaHyun Ah Woo, Seong Heon Kim, Yo Han Ahn, et al.
Pediatric Nephrology (Berlin, Germany)|August 31, 2010
Variable renal phenotype in a family with an INF2 mutationHyun Kyung Lee, Kyoung Hee Han, Yun Hye Jung, et al.
Pediatric Nephrology (Berlin, Germany)|September 5, 2006
Idiopathic membranous nephropathy in childrenBeom Hee Lee, Hee Yeon Cho, Hee Gyung Kang, et al.
Kidney Research and Clinical Practice|October 21, 2015
MYH9 nephropathyTaehoon Oh, Hyun Jung Seo, Kyu Taek Lee, et al.
Kidney Research and Clinical Practice|January 9, 2019
Acute kidney injury in childhood-onset nephrotic syndrome: Incidence and risk factors in hospitalized patientsMi Young Kim, Myung Hyun Cho, Ji Hyun Kim, et al.
Pediatric Nephrology (Berlin, Germany)|May 16, 2008
Congenital thrombotic thrombocytopenic purpura associated with unilateral moyamoya diseaseHye Won Park, Doyeon Oh, Namkeun Kim, et al.
Experimental Cell Research|January 14, 2014
Calpain-mediated proteolysis of polycystin-1 C-terminus induces JAK2 and ERK signal alterationsHyunho Kim, Ah-Young Kang, Ah-ra Ko, et al.
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