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pro vyhledávání: '"K. J. Robbins"'
Publikováno v:
Case Reports in Hematology, Vol 2016 (2016)
Introduction. Hemophagocytic lymphohistiocytosis (HLH) is a rare hyperinflammatory syndrome that can be associated with inherited genetic mutations, malignancy, autoimmune disorders, and viral infections. Though the pathogenesis is not fully known, H
Externí odkaz:
https://doaj.org/article/e929ed89af824a4b8c1390d12f74f6f1