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Zhenle Yang

Showing results (21-30 of 28) with videos related to

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Frontiers in Medicine|February 16, 2026
An unusual trilogy: a case of comorbid aHUS, Fabry disease, and hypertrophic cardiomyopathyQian Li, Lichun Yu, Jing Wang, et al.
BMC Pediatrics|November 23, 2023
A novel mutation of the RPGRIP1L gene in a Chinese boy with Joubert syndrome with oculorenal involvementQian Li, Qianying Liu, Suwen Liu, et al.
Renal Failure|May 10, 2024
Clinical features and genetic analysis of 15 Chinese children with dent diseaseQian Li, Zhenle Yang, Ruixian Zang, et al.
Frontiers in Pediatrics|February 23, 2023
Clinical features and enzyme replacement therapy in 10 children with Fabry diseaseQian Li, Jing Wang, Minle Tian, et al.
Renal Failure|June 22, 2022
Clinical features of children with anti-CFH autoantibody-associated hemolytic uremic syndrome: a report of 8 casesQian Li, Xinxin Kong, Minle Tian, et al.
Scientific Reports|February 3, 2026
Polygenic risk score from steroid-sensitive nephrotic syndrome GWAS indicates overlapping genetic basis with steroid-resistant casesCong Wang, Guotao Yin, Yidi Zhou, et al.
Frontiers in Immunology|June 15, 2026
Identification of <i>IL7R</i> as a key genetic risk locus in childhood steroid-sensitive nephrotic syndrome and IgA nephropathyCong Wang, Yue Jiang, Yingchao Song, et al.
Journal of the American Society of Nephrology : JASN|September 12, 2025
Mycophenolate Mofetil versus Cyclophosphamide for Initial Therapy in Childhood-Onset Proliferative Lupus Nephritis: A Prospective, Multicenter, Randomized TrialYing Wang, Xiaoyan Li, Shan Jian, et al.
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Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Frontiers in Medicine|February 16, 2026
An unusual trilogy: a case of comorbid aHUS, Fabry disease, and hypertrophic cardiomyopathyQian Li, Lichun Yu, Jing Wang, et al.
BMC Pediatrics|November 23, 2023
A novel mutation of the RPGRIP1L gene in a Chinese boy with Joubert syndrome with oculorenal involvementQian Li, Qianying Liu, Suwen Liu, et al.
Renal Failure|May 10, 2024
Clinical features and genetic analysis of 15 Chinese children with dent diseaseQian Li, Zhenle Yang, Ruixian Zang, et al.
Frontiers in Pediatrics|February 23, 2023
Clinical features and enzyme replacement therapy in 10 children with Fabry diseaseQian Li, Jing Wang, Minle Tian, et al.
Renal Failure|June 22, 2022
Clinical features of children with anti-CFH autoantibody-associated hemolytic uremic syndrome: a report of 8 casesQian Li, Xinxin Kong, Minle Tian, et al.
Scientific Reports|February 3, 2026
Polygenic risk score from steroid-sensitive nephrotic syndrome GWAS indicates overlapping genetic basis with steroid-resistant casesCong Wang, Guotao Yin, Yidi Zhou, et al.
Frontiers in Immunology|June 15, 2026
Identification of <i>IL7R</i> as a key genetic risk locus in childhood steroid-sensitive nephrotic syndrome and IgA nephropathyCong Wang, Yue Jiang, Yingchao Song, et al.
Journal of the American Society of Nephrology : JASN|September 12, 2025
Mycophenolate Mofetil versus Cyclophosphamide for Initial Therapy in Childhood-Onset Proliferative Lupus Nephritis: A Prospective, Multicenter, Randomized TrialYing Wang, Xiaoyan Li, Shan Jian, et al.
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