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Coagulation disorders in patients with severe hemophagocytic lymphohistiocytosis

34

Citations

33

References

2021

Year

Abstract

Hyperfibrinolysis may be the primary mechanism responsible for hypofibrinogenemia and may also participate in ADAMTS13 degradation. Targeting the plasmin system appears as a promising approach in severe HLH-related coagulation disorders.

References

YearCitations

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