Ruxolitinib for refractory/relapsed hemophagocytic lymphohistiocytosis

2019 
Hemophagocytic lymphohistiocytosis (HLH) is a clinical syndrome associated with hereditary or acquired immune-dysregulation. HLH is classified into either primary or secondary disease based on whether or not clear genetic defects are present. Patients of primary HLH have clear hereditary or genetic
    • Correction
    • Source
    • Cite
    • Save
    • Machine Reading By IdeaReader
    15
    References
    37
    Citations
    NaN
    KQI
    []