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Stéphane Decramer

Showing results (91-100 of 107) with videos related to

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Kidney International Reports|September 12, 2022
Refining Kidney Survival in 383 Genetically Characterized Patients With NephronophthisisJens Christian König, Rebeka Karsay, Joachim Gerß, et al.
Clinical Journal of the American Society of Nephrology : CJASN|February 27, 2015
CKD and Its Risk Factors among Patients with CystinuriaCaroline Prot-Bertoye, Saïd Lebbah, Michel Daudon, et al.
BJU International|February 26, 2019
Adverse events associated with currently used medical treatments for cystinuria and treatment goals: results from a series of 442 patients in FranceCaroline Prot-Bertoye, Saïd Lebbah, Michel Daudon, et al.
Journal of the American Society of Nephrology : JASN|October 5, 2021
Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNADaan Viering, Karl P Schlingmann, Marguerite Hureaux, et al.
Nature Communications|September 5, 2019
Defects in t<sup>6</sup>A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndromeChristelle Arrondel, Sophia Missoury, Rozemarijn Snoek, et al.
Journal of the American Society of Nephrology : JASN|April 7, 2017
Clinical and Genetic Spectrum of Bartter Syndrome Type 3Elsa Seys, Olga Andrini, Mathilde Keck, et al.
The Lancet. Rheumatology|January 24, 2024
Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohortsAlexandre Belot, Gillian I Rice, Sulliman Ommar Omarjee, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 6, 2026
The European distal renal tubular acidosis registry: a five-year analysisMarta Giaccari, Faidra Veligratli, Wesley Hayes, et al.
Molecular & Cellular Proteomics : MCP|July 10, 2010
Naturally occurring human urinary peptides for use in diagnosis of chronic kidney diseaseDavid M Good, Petra Zürbig, Angel Argilés, et al.
Kidney International Reports|August 19, 2024
Renal and Extrarenal Phenotypes in Patients With <i>HNF1B</i> Variants and Chromosome 17q12 MicrodeletionsBénédicte Buffin-Meyer, Juliette Richard, Vincent Guigonis, et al.
Pageof 11

Showing results (91-100 of 107) with videos related to

Sort By:
Pageof 11
Kidney International Reports|September 12, 2022
Refining Kidney Survival in 383 Genetically Characterized Patients With NephronophthisisJens Christian König, Rebeka Karsay, Joachim Gerß, et al.
Clinical Journal of the American Society of Nephrology : CJASN|February 27, 2015
CKD and Its Risk Factors among Patients with CystinuriaCaroline Prot-Bertoye, Saïd Lebbah, Michel Daudon, et al.
BJU International|February 26, 2019
Adverse events associated with currently used medical treatments for cystinuria and treatment goals: results from a series of 442 patients in FranceCaroline Prot-Bertoye, Saïd Lebbah, Michel Daudon, et al.
Journal of the American Society of Nephrology : JASN|October 5, 2021
Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNADaan Viering, Karl P Schlingmann, Marguerite Hureaux, et al.
Nature Communications|September 5, 2019
Defects in t<sup>6</sup>A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndromeChristelle Arrondel, Sophia Missoury, Rozemarijn Snoek, et al.
Journal of the American Society of Nephrology : JASN|April 7, 2017
Clinical and Genetic Spectrum of Bartter Syndrome Type 3Elsa Seys, Olga Andrini, Mathilde Keck, et al.
The Lancet. Rheumatology|January 24, 2024
Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohortsAlexandre Belot, Gillian I Rice, Sulliman Ommar Omarjee, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 6, 2026
The European distal renal tubular acidosis registry: a five-year analysisMarta Giaccari, Faidra Veligratli, Wesley Hayes, et al.
Molecular & Cellular Proteomics : MCP|July 10, 2010
Naturally occurring human urinary peptides for use in diagnosis of chronic kidney diseaseDavid M Good, Petra Zürbig, Angel Argilés, et al.
Kidney International Reports|August 19, 2024
Renal and Extrarenal Phenotypes in Patients With <i>HNF1B</i> Variants and Chromosome 17q12 MicrodeletionsBénédicte Buffin-Meyer, Juliette Richard, Vincent Guigonis, et al.
Pageof 11