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Pediatric Nephrology (Berlin, Germany)|March 15, 2018
Outcome of renal transplantation in small infants: a match-controlled analysisMarcus Weitz, Guido F Laube, Maria Schmidt, 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.Journal of the American Society of Nephrology : JASN|January 15, 2022
Claudin-10a Deficiency Shifts Proximal Tubular Cl- Permeability to Cation Selectivity via Claudin-2 RedistributionTilman Breiderhoff, Nina Himmerkus, Luca Meoli, et al.Journal of Visualized Experiments : Jove|January 6, 2025
Operating and Biocontainment Procedures of a Facility for Laboratory Mice with a Natural Microbiome: Immunophenotyping ProcedureNatascha Drude, Kai Diederich, Claudia U Duerr, et al.International Journal of Molecular Sciences|December 18, 2019
Structural Insights into the Intracellular Region of the Human Magnesium Transport Mediator CNNM4Paula Giménez-Mascarell, Iker Oyenarte, Irene González-Recio, et al.Journal of the American Society of Nephrology : JASN|August 23, 2002
Cell-biologic and functional analyses of five new Aquaporin-2 missense mutations that cause recessive nephrogenic diabetes insipidusNannette Marr, Daniel G Bichet, Susan Hoefs, et al.Journal of the American Society of Nephrology : JASN|November 17, 2019
TBC1D8B Mutations Implicate RAB11-Dependent Vesicular Trafficking in the Pathogenesis of Nephrotic SyndromeLina L Kampf, Ronen Schneider, Lea Gerstner, et al.Pediatric Rheumatology Online Journal|September 26, 2023
Treat-to-target strategies for the management of familial Mediterranean Fever in childrenLisa Ehlers, Elisabeth Rolfes, Mareike Lieber, et al.Bioorganic & Medicinal Chemistry Letters|May 22, 2009
Design and optimization of renin inhibitors: Orally bioavailable alkyl aminesColin M Tice, Zhenrong Xu, Jing Yuan, et al.Human Mutation|February 18, 2021
The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2)Gijs A C Franken, Dominik Müller, Cyril Mignot, et al.Pageof 32