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Romiplostim in children with newly diagnosed or persistent primary immune thrombocytopenia

Immune thrombocytopenia (ITP) is a disease of heterogenous origin characterized by low platelet counts and an increased bleeding tendency. Three disease phases have been described: newly diagnosed (≤ 3 months after diagnosis), persistent (> 3–12 months after diagnosis), and chronic (> 12 month...

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Detalhes bibliográficos
Publicado no:Ann Hematol
Main Authors: Grainger, John D., Kühne, Thomas, Hippenmeyer, Jane, Cooper, Nichola
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8310729/
https://ncbi.nlm.nih.gov/pubmed/34308495
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00277-021-04590-0
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