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Routine hemostasis profile in steady state sickle cell disease adult patients compared to laboratory values, between phenotypes and during pregnancy: A retrospective, descriptive study

Abstract Sickle cell disease is a rare genetic disease resulting from an abnormality in hemoglobin. Hemostasis in the steady state, defined as ≥2 months without vaso‐occlusive crises, is poorly described in the literature. We report the routine hemostasis profile in steady state patients with sickle...

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Bibliografski detalji
Glavni autori: Comlan Affo, Carine Schmidt, Antoine Bosquet, Bénédicte Dumont, Isabelle Mahé
Format: Artigo
Jezik:Inglês
Izdano: Wiley 2024-10-01
Serija:eJHaem
Teme:
Online pristup:https://doi.org/10.1002/jha2.876
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