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The Journal of Clinical Investigation|May 5, 2010
PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndromeInga Ebermann, Jennifer B Phillips, Max C Liebau, et al.
Pediatric Nephrology (Berlin, Germany)|February 4, 2025
Urinary Dickkopf-related protein 3 as a novel biomarker for kidney function decline in children with Alport syndromeJan Boeckhaus, Burkhard Tönshoff, Lutz T Weber, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|March 23, 2017
Intermediate Follow-up of Pediatric Patients With Hemolytic Uremic Syndrome During the 2011 Outbreak Caused by E. coli O104:H4Sebastian Loos, Wiebke Aulbert, Bernd Hoppe, et al.
Scientific Reports|May 30, 2019
Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)Kathrin Burgmaier, Samuel Kilian, Bert Bammens, et al.
Experimental & Molecular Medicine|July 1, 2018
Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalusClaudia Dafinger, Markus M Rinschen, Lori Borgal, et al.
Nature Reviews. Nephrology|May 24, 2019
International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young peopleCharlotte Gimpel, Carsten Bergmann, Detlef Bockenhauer, et al.
Kidney International|March 14, 2018
Single-nephron proteomes connect morphology and function in proteinuric kidney diseaseMartin Höhne, Christian K Frese, Florian Grahammer, et al.
Nature Metabolism|July 23, 2020
A molecular mechanism explaining albuminuria in kidney diseaseLinus Butt, David Unnersjö-Jess, Martin Höhne, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 30, 2022
Definition, diagnosis and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet Working Group on Kidney MalformationsStefan Kohl, Fred E Avni, Peter Boor, et al.
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