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Publikováno v:
Pathology. 29:92-95
Clinical course and histopathologic features of a typical case of familial hemophagocytic lymphohistiocytosis (FHLH) are presented. FHLH, initially known as familial hemophagocytic reticulosis (FHR), is rare and without proper treatment is invariably
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7416ecfe13a846d91fc84898e6c6de37
https://doi.org/10.1080/00313029700169644
https://doi.org/10.1080/00313029700169644
