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World Journal of Pediatrics : WJP|June 1, 2021
Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease DatabaseJia-Lu Liu, Qian Shen, Ming-Yan Wu, et al.The Journal of Clinical Investigation|October 24, 2017
Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndromeJia Rao, Shazia Ashraf, Weizhen Tan, et al.Kidney International|June 1, 2022
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiencyStefania Drovandi, Beata S Lipska-Ziętkiewicz, Fatih Ozaltin, et al.Kidney International|April 28, 2022
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathyStefania Drovandi, Beata S Lipska-Ziętkiewicz, Fatih Ozaltin, et al.Journal of the American Society of Nephrology : JASN|February 17, 2021
Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat SyndromeNina Mann, Slim Mzoughi, Ronen Schneider, et al.Clinical Genetics|July 23, 2019
Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration systemJia Rao, Xiaorong Liu, Jianhua Mao, et al.The Journal of Clinical Investigation|September 5, 2018
Mutations in multiple components of the nuclear pore complex cause nephrotic syndromeDaniela A Braun, Svjetlana Lovric, David Schapiro, et al.Phenomics (Cham, Switzerland)|March 20, 2023
Genetic Architecture of Childhood Kidney and Urological Diseases in ChinaYe Fang, Hua Shi, Tianchao Xiang, et al.The Journal of Clinical Investigation|February 7, 2017
Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiencySvjetlana Lovric, Sara Goncalves, Heon Yung Gee, et al.Clinical Journal of the American Society of Nephrology : CJASN|November 12, 2017
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic SyndromeJillian K Warejko, Weizhen Tan, Ankana Daga, et al.Pageof 13