Microvascular oxygen consumption during sickle cell pain crisis

Sickle cell disease is an inherited blood disorder characterized by chronic hemolytic anemia and episodic vaso-occlusive pain crises. Vaso-occlusion occurs when deoxygenated hemoglobin S polymerizes and erythrocytes sickle and adhere in the microvasculature, a process dependent on the concentration...

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Autors principals: Rowley, Carol A., Ikeda, Allison K., Seidel, Miles, Anaebere, Tiffany C., Antalek, Matthew D., Seamon, Catherine, Conrey, Anna K., Mendelsohn, Laurel, Nichols, James, Gorbach, Alexander M., Kato, Gregory J., Ackerman, Hans
Format: Artigo
Idioma:Inglês
Publicat: American Society of Hematology 2014
Matèries:
Clinical Trials and Observations
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4023418/
https://ncbi.nlm.nih.gov/pubmed/24665133
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2013-11-533406
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