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Roser Torra

Showing results (151-160 of 161) with videos related to

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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 7, 2024
Inherited kidney disease and CAKUT are common causes of kidney failure requiring kidney replacement therapy: an ERA Registry studyAlberto Ortiz, Anneke Kramer, Gema Ariceta, et al.
Kidney International|May 26, 2020
Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1Eric Olinger, Patrick Hofmann, Kendrah Kidd, et al.
Kidney International|February 21, 2024
Reassuring pregnancy outcomes in women with mild COL4A3-5-related disease (Alport syndrome) and genetic type of disease can aid personalized counselingMargriet E Gosselink, Rozemarijn Snoek, Agne Cerkauskaite-Kerpauskiene, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 28, 2024
Clinical Spectrum and Prognosis of Atypical Autosomal Dominant Polycystic Kidney Disease Caused by Monoallelic Pathogenic Variants of IFT140Nikola Zagorec, Alizée Calamel, Margaux Delaporte, et al.
Nephron|September 7, 2016
International Multi-Specialty Delphi Survey: Identification of Diagnostic Criteria for Hepatic and Renal Cyst InfectionMarten A Lantinga, Alexander J M Darding, Ruud G L de Sévaux, et al.
The Lancet. Gastroenterology & Hepatology|June 15, 2024
Clinical management of liver cyst infections: an international, modified Delphi-based clinical decision frameworkRenée Duijzer, Lucas H P Bernts, Anja Geerts, et al.
Kidney International|January 23, 2025
KDIGO 2025 clinical practice guideline for the evaluation, management, and treatment of autosomal dominant polycystic kidney disease (ADPKD): executive summaryVicente E Torres, Curie Ahn, Thijs R M Barten, et al.
Nature Genetics|March 30, 2007
Analysis of published PKD1 gene sequence variantsAlexander M Gout, , David Ravine, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 19, 2016
Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: report from the 2015 International Workshop on Alport SyndromeOliver Gross, Clifford E Kashtan, Michelle N Rheault, et al.
The New England Journal of Medicine|August 11, 2016
Treatment of Fabry's Disease with the Pharmacologic Chaperone MigalastatDominique P Germain, Derralynn A Hughes, Kathleen Nicholls, et al.
Pageof 17

Showing results (151-160 of 161) with videos related to

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Pageof 17
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 7, 2024
Inherited kidney disease and CAKUT are common causes of kidney failure requiring kidney replacement therapy: an ERA Registry studyAlberto Ortiz, Anneke Kramer, Gema Ariceta, et al.
Kidney International|May 26, 2020
Clinical and genetic spectra of autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD and MUC1Eric Olinger, Patrick Hofmann, Kendrah Kidd, et al.
Kidney International|February 21, 2024
Reassuring pregnancy outcomes in women with mild COL4A3-5-related disease (Alport syndrome) and genetic type of disease can aid personalized counselingMargriet E Gosselink, Rozemarijn Snoek, Agne Cerkauskaite-Kerpauskiene, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 28, 2024
Clinical Spectrum and Prognosis of Atypical Autosomal Dominant Polycystic Kidney Disease Caused by Monoallelic Pathogenic Variants of IFT140Nikola Zagorec, Alizée Calamel, Margaux Delaporte, et al.
Nephron|September 7, 2016
International Multi-Specialty Delphi Survey: Identification of Diagnostic Criteria for Hepatic and Renal Cyst InfectionMarten A Lantinga, Alexander J M Darding, Ruud G L de Sévaux, et al.
The Lancet. Gastroenterology & Hepatology|June 15, 2024
Clinical management of liver cyst infections: an international, modified Delphi-based clinical decision frameworkRenée Duijzer, Lucas H P Bernts, Anja Geerts, et al.
Kidney International|January 23, 2025
KDIGO 2025 clinical practice guideline for the evaluation, management, and treatment of autosomal dominant polycystic kidney disease (ADPKD): executive summaryVicente E Torres, Curie Ahn, Thijs R M Barten, et al.
Nature Genetics|March 30, 2007
Analysis of published PKD1 gene sequence variantsAlexander M Gout, , David Ravine, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 19, 2016
Advances and unmet needs in genetic, basic and clinical science in Alport syndrome: report from the 2015 International Workshop on Alport SyndromeOliver Gross, Clifford E Kashtan, Michelle N Rheault, et al.
The New England Journal of Medicine|August 11, 2016
Treatment of Fabry's Disease with the Pharmacologic Chaperone MigalastatDominique P Germain, Derralynn A Hughes, Kathleen Nicholls, et al.
Pageof 17