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Gerald B Appel

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Clinical Journal of the American Society of Nephrology : CJASN|December 15, 2015

Complete Remission in the Nephrotic Syndrome Study NetworkDebbie S Gipson, Jonathan P Troost, Richard A Lafayette, et al.

Kidney International|November 28, 2022

Precision nephrology identified tumor necrosis factor activation variability in minimal change disease and focal segmental glomerulosclerosisLaura H Mariani, Sean Eddy, Fadhl M AlAkwaa, et al.

Medrxiv : the Preprint Server for Health Sciences|August 14, 2023

Strong protective effect of the <i>APOL1</i> p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney diseaseYask Gupta, David J Friedman, Michelle McNulty, et al.

Journal of the American Society of Nephrology : JASN|March 30, 2023

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic DiagnosisDina F Ahram, Tze Y Lim, Juntao Ke, et al.

Nature Communications|November 30, 2023

Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney diseaseYask Gupta, David J Friedman, Michelle T McNulty, et al.

Medrxiv : the Preprint Server for Health Sciences|October 17, 2024

Genome-wide studies define new genetic mechanisms of IgA vasculitisLili Liu, Li Zhu, Sara Monteiro-Martins, et al.

Nature Communications|October 9, 2025

Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genesHila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, et al.

Nature Communications|August 7, 2025

Exome analysis links kidney malformations to developmental disorders and reveals causal genesHila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, et al.

Nature Communications|April 2, 2020

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosisJingyuan Xie, Lili Liu, Nikol Mladkova, et al.

Nature Genetics|June 19, 2023

Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathyKrzysztof Kiryluk, Elena Sanchez-Rodriguez, Xu-Jie Zhou, et al.

Pageof 14

Search research articles

Showing results (131-140 of 140) with videos related to

Sort By:

Pageof 14

You have reached the last page of results.This site can display upto 140 results.

Clinical Journal of the American Society of Nephrology : CJASN|December 15, 2015

Complete Remission in the Nephrotic Syndrome Study NetworkDebbie S Gipson, Jonathan P Troost, Richard A Lafayette, et al.

Kidney International|November 28, 2022

Precision nephrology identified tumor necrosis factor activation variability in minimal change disease and focal segmental glomerulosclerosisLaura H Mariani, Sean Eddy, Fadhl M AlAkwaa, et al.

Medrxiv : the Preprint Server for Health Sciences|August 14, 2023

Strong protective effect of the <i>APOL1</i> p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney diseaseYask Gupta, David J Friedman, Michelle McNulty, et al.

Journal of the American Society of Nephrology : JASN|March 30, 2023

Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic DiagnosisDina F Ahram, Tze Y Lim, Juntao Ke, et al.

Nature Communications|November 30, 2023

Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney diseaseYask Gupta, David J Friedman, Michelle T McNulty, et al.

Medrxiv : the Preprint Server for Health Sciences|October 17, 2024

Genome-wide studies define new genetic mechanisms of IgA vasculitisLili Liu, Li Zhu, Sara Monteiro-Martins, et al.

Nature Communications|October 9, 2025

Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genesHila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, et al.

Nature Communications|August 7, 2025

Exome analysis links kidney malformations to developmental disorders and reveals causal genesHila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, et al.

Nature Communications|April 2, 2020

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosisJingyuan Xie, Lili Liu, Nikol Mladkova, et al.

Nature Genetics|June 19, 2023

Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathyKrzysztof Kiryluk, Elena Sanchez-Rodriguez, Xu-Jie Zhou, et al.

Pageof 14