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A novel prognostic model for adult patients with Hemophagocytic Lymphohistiocytosis

BACKGROUND: Hemophagocytic Lymphohistiocytosis (HLH) is a type of rare disease with low survival rate. We aimed to develop a model to evaluate the six-month prognosis in adult HLH patients. The data at discharge (will be called as post-treatment) for newly diagnosed adult HLH patients was collected...

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Detaylı Bibliyografya
Yayımlandı:Orphanet J Rare Dis
Asıl Yazarlar: Zhou, Jun, Zhou, Jing, Wu, Zhi-Qi, Goyal, Hemant, Xu, Hua-Guo
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2020
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7439554/
https://ncbi.nlm.nih.gov/pubmed/32819431
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-020-01496-4
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