## Background and procedure: The etiology of familial hemophagocytic lymphohistiocytosis (fhl), which is characterized by fever, hepatosplenomegaly, pancytopenia, and coagulopathy, remains unknown. we analyzed 43 fhl patients, all with affected siblings, in 18 families who were identified during th
✦ LIBER ✦
Familial hemophagocytic lymphohistiocytosis: clinical and neuroradiological findings and review of the literature
✍ Scribed by Norma Decaminada; Maria Cappellini; Marzia Mortilla; Erica Del Giudice; Elena Sieni; Desireè Caselli; Maurizio Aricò; Claudio Fonda
- Publisher
- Springer
- Year
- 2009
- Tongue
- English
- Weight
- 368 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0256-7040
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