Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 3, 2005
Successful plasma therapy for atypical hemolytic uremic syndrome caused by factor H deficiency owing to a novel mutation in the complement cofactor protein domain 15Christoph Licht, Annic Weyersberg, Stefan Heinen, et al.
Frontiers in Pediatrics|November 29, 2023
Two sides of the same coin: a complex presentation of autosomal dominant tubulointerstitial kidney diseases: a literature review and case reportsMargareta Fistrek Prlic, Sanda Huljev Frkovic, Bodo Beck, et al.
Nephron|May 24, 2018
A de novo KCNA1 Mutation in a Patient with Tetany and HypomagnesemiaJenny van der Wijst, Martin Konrad, Sjoerd A J Verkaart, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 29, 2022
Alport syndrome and autosomal dominant tubulointerstitial kidney disease frequently underlie end-stage renal disease of unknown origin-a single-center analysisEsther Leenen, Florian Erger, Janine Altmüller, et al.
Frontiers in Nephrology|March 6, 2024
A multi-center interventional study to assess pharmacokinetics, effectiveness, and tolerability of prolonged-release tacrolimus after pediatric kidney transplantation: study protocol for a prospective, open-label, randomized, two-phase, two-sequence, single dose, crossover, phase III b trialSinem Karaterzi, Burkhard Tönshoff, Thurid Ahlenstiel-Grunow, et al.
Genome Medicine|August 23, 2023
Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletionsNikolai Tschernoster, Florian Erger, Stefan Kohl, et al.
Kidney International|December 15, 2011
Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancyOliver Gross, Christoph Licht, Hans J Anders, et al.
Molecular Genetics & Genomic Medicine|September 26, 2017
Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and <i>PEX26</i> mutated in Heimler syndromeChristine Neuhaus, Tobias Eisenberger, Christian Decker, et al.
Pageof 2