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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.Radiology|January 2, 2019
Imaging of Kidney Cysts and Cystic Kidney Diseases in Children: An International Working Group Consensus StatementCharlotte Gimpel, E Fred Avni, Luc Breysem, 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.Pageof 9