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Blood|August 19, 2020
Management of thrombotic microangiopathy in pregnancy and postpartum: report from an international working groupFadi Fakhouri, Marie Scully, François Provôt, et al.
Journal of the American Society of Nephrology : JASN|December 16, 2016
Thrombotic Microangiopathy in Inverted Formin 2-Mediated Renal DiseaseRachel C Challis, Troels Ring, Yaobo Xu, et al.
Investigative Ophthalmology & Visual Science|July 2, 2010
Complement factor h autoantibodies and age-related macular degenerationBaljean Dhillon, Alan F Wright, Adnan Tufail, et al.
Health Technology Assessment (Winchester, England)|March 3, 2026
Clinical and cost-effectiveness of eculizumab withdrawal in atypical haemolytic uraemic syndrome: the SETS aHUS multi-centre, open-label, prospective and single-arm studyAndrew Bryant, Jan Lecouturier, Giovany Orozco-Leal, et al.
Kidney Medicine|August 6, 2024
Ravulizumab in Atypical Hemolytic Uremic Syndrome: An Analysis of 2-Year Efficacy and Safety Outcomes in 2 Phase 3 TrialsBradley P Dixon, David Kavanagh, Alvaro Domingo Madrid Aris, et al.
Human Mutation|June 21, 2021
Prevalence and phenotype associations of complement factor I mutations in geographic atrophyAdnan H Khan, Janice Sutton, Angela J Cree, et al.
Molecular Immunology|June 23, 2012
Factor H autoantibodies in membranoproliferative glomerulonephritisTimothy H J Goodship, Isabel Y Pappworth, Tibor Toth, et al.
Nature Communications|October 12, 2018
Complement receptor CD46 co-stimulates optimal human CD8+ T cell effector function via fatty acid metabolismGiuseppina Arbore, Erin E West, Jubayer Rahman, et al.
Nature Reviews. Nephrology|January 30, 2019
C3 glomerulopathy - understanding a rare complement-driven renal diseaseRichard J H Smith, Gerald B Appel, Anna M Blom, et al.
Journal of the American Society of Nephrology : JASN|April 12, 2014
Characterization of a factor H mutation that perturbs the alternative pathway of complement in a family with membranoproliferative GNEdwin K S Wong, Holly E Anderson, Andrew P Herbert, et al.
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