Immunoadsorption and autologous transplantation for life-threatening primary antiphospholipid syndrome

Reduction of APL antibodies by immunoadsorption may be a lifesaving therapy for the management of DAH with high titer of APL antibodies. Autologous HSCT may be a valid treatment option in patients with primary APS and no response to standard immunosuppressive therapy.

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Bibliografiske detaljer
Udgivet i:Blood Adv
Main Authors: Angelillo-Scherrer, Anne, Mansouri Taleghani, Behrouz, Förger, Frauke, Baerlocher, Gabriela M., Pabst, Thomas, Pöllinger, Alexander, Banz, Yara, Geiser, Thomas, Kremer Hovinga, Johanna A., Rovó, Alicia
Format: Artigo
Sprog:Inglês
Udgivet: American Society of Hematology 2019
Fag:
Exceptional Case Report
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6737408/
https://ncbi.nlm.nih.gov/pubmed/31506284
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2019000465
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