2018•Transplantation ProceedingsRequires access

Successful 7-Year Eculizumab Treatment of Plasmapheresis-Resistant Recurrent Atypical Hemolytic-Uremic Syndrome due to Complement Factor H Hybrid Gene: A Case Report

Karel Vondrák, Tomáš Seeman

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Key concepts: Eculizumab, Atypical hemolytic uremic syndrome, Factor H, Plasmapheresis, Medicine, Complement factor I, Transplantation, Kidney transplantation

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Successful 7-Year Eculizumab Treatment of Plasmapheresis-Resistant Recurrent Atypical Hemolytic-Uremic Syndrome due to Complement Factor H Hybrid Gene: A Case Report — Research Paper | ScholarLens