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Clinical Kidney Journal|January 4, 2021
How genomics reclassifies diseases: the case of Alport syndromeRoser Torra, Monica Furlano, Elisabet Ars
Nefrologia|September 26, 2025
Phenotypic variability in cystinosis: Lessons from an atypical caseDiego Toso, Monica Furlano, Adria Tinoco, et al.
Clinical Kidney Journal|December 4, 2023
Artificial intelligence: a new field of knowledge for nephrologists?Leonor Fayos De Arizón, Elizabeth R Viera, Melissa Pilco, et al.
Stem Cell Research|November 19, 2017
Generation of integration-free induced pluripotent stem cell lines derived from two patients with X-linked Alport syndrome (XLAS)Bernd Kuebler, Begoña Aran, Laia Miquel-Serra, et al.
Stem Cell Research|December 17, 2017
Integration-free induced pluripotent stem cells derived from a patient with autosomal recessive Alport syndrome (ARAS)Bernd Kuebler, Begoña Aran, Laia Miquel-Serra, et al.
Clinical Kidney Journal|February 24, 2023
Flank pain has a significant adverse impact on quality of life in ADPKD: the CYSTic-QoL studyJean Winterbottom, Roslyn J Simms, Anna Caroli, et al.
Kidney International Reports|February 12, 2024
An Artificial Intelligence Generated Automated Algorithm to Measure Total Kidney Volume in ADPKDJonathan Taylor, Richard Thomas, Peter Metherall, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 23, 2025
Nephrectomy in autosomal dominant polycystic kidney disease: a consensus statement of the ERA Genes & Kidney Working GroupPaul Geertsema, Ron T Gansevoort, Mustafa Arici, 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.
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