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Pediatric Nephrology (Berlin, Germany)|November 26, 2015
Liver transplantation for aHUS: still needed in the eculizumab era?Rosanna Coppo, Roberto Bonaudo, R Licia Peruzzi, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 15, 2021
Genetic testing in the diagnosis of chronic kidney disease: recommendations for clinical practiceNine Knoers, Corinne Antignac, Carsten Bergmann, et al.
Thrombosis and Haemostasis|March 1, 2005
Complement activation: the missing link between ADAMTS-13 deficiency and microvascular thrombosis of thrombotic microangiopathiesMaria Piedad Ruiz-Torres, Federica Casiraghi, Miriam Galbusera, et al.
Nephron|March 20, 2019
Hemolytic Uremic Syndrome in an Infant with Primary Hyperoxaluria Type II: An Unreported Clinical AssociationElisabetta Valoti, Marta Alberti, Camillo Carrara, et al.
Molecular Immunology|August 3, 2006
Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndromeAnna Richards, M Kathryn Liszewski, David Kavanagh, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 12, 2022
Therapeutic Small Interfering RNA Targeting Complement C3 in a Mouse Model of C3 GlomerulopathyCristina Zanchi, Monica Locatelli, Domenico Cerullo, et al.
Frontiers in Immunology|February 27, 2023
An ex vivo test to investigate genetic factors conferring susceptibility to atypical haemolytic uremic syndromeSara Gastoldi, Sistiana Aiello, Miriam Galbusera, et al.
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