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Managing transient immune complex reactions in patients with paroxysmal nocturnal hemoglobinuria: clinical observations from the COMMODORE 1 and 2 studies. [PDF]
Kulasekararaj AG +9 more
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Immunotherapies in neuromyelitis optica: Bayesian network meta-analysis. [PDF]
John N +8 more
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Iptacopan in C5 blockade refractory atypical hemolytic uremic syndrome with associated Castleman's disease: case report. [PDF]
Nguyen MD +10 more
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Monitoring Ravulizumab effect on complement assays
Journal of Immunological Methods, 2021Ravulizumab is a new C5 inhibitor therapeutic monoclonal antibody with a longer half-life than eculizumab. Monitoring complete complement blockade by eculizumab has allowed personalized therapy in specific settings. Similar action is expected with ravulizumab. Ravulizumab has 4 different amino acids from eculizumab, which allow greater affinity for the
Paula M Ladwig
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Terminal Complement Inhibitor Ravulizumab in Generalized Myasthenia Gravis
NEJM Evidence, 2022BACKGROUND: Generalized myasthenia gravis (gMG) is a rare, chronic, and debilitating autoimmune disease. Activation of the complement system by autoantibodies against the postsynaptic acetylcholine receptor (AChR) leads to destruction of the postsynaptic membrane and disruption of neuromuscular transmission.
Tuan Vu +2 more
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Ravulizumab for the treatment of paroxysmal nocturnal hemoglobinuria
Expert Opinion on Biological Therapy, 2020Introduction: Eculizumab, which is indicated to treat patients with paroxysmal nocturnal hemoglobinuria (PNH), is a life-changing, life-saving therapy that decreases intravascular hemolysis and thrombosis and improves survival. Some eculizumab-treated patients, however, experience breakthrough hemolysis; and overall, the burden of the treatment ...
Jong Wook Lee, Austin G Kulasekararaj
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