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Stroke and presence of patent foramen ovale in sickle cell disease

Sickle cell disease (SCD) is an inherited monogenic hemoglobinopathy characterized by formation of sickle erythrocytes under conditions of deoxygenation. Sickle erythrocytes can lead to thrombus formation and vaso-occlusive episodes that may result in hemolytic anemia, pain crisis and multiple organ...

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Bibliografski detalji
Izdano u:J Thromb Thrombolysis
Glavni autori: Aggeli, Constantina, Polytarchou, Kali, Dimitroglou, Yannis, Patsourakos, Dimitrios, Delicou, Sophia, Vassilopoulou, Sophia, Tsiamis, Eleftherios, Tsioufis, Kostas
Format: Artigo
Jezik:Inglês
Izdano: Springer US 2021
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7909731/
https://ncbi.nlm.nih.gov/pubmed/33638018
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11239-021-02398-3
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