Showing results (251-260 of 282) with videos related to
Sort By:
Pageof 29
American Journal of Human Genetics|March 15, 2011
CNNM2, encoding a basolateral protein required for renal Mg2+ handling, is mutated in dominant hypomagnesemiaMarchel Stuiver, Sergio Lainez, Constanze Will, et al.Pediatric Nephrology (Berlin, Germany)|January 23, 2019
HNF1B nephropathy has a slow-progressive phenotype in childhood-with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood RegistryChristine Okorn, Anne Goertz, Udo Vester, et al.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.Pageof 29