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Measuring Pain in Sickle Cell Disease using Clinical Text

Sickle Cell Disease (SCD) is a hereditary disorder of red blood cells in humans. Complications such as pain, stroke, and organ failure occur in SCD as malformed, sickled red blood cells passing through small blood vessels get trapped. Particularly, acute pain is known to be the primary symptom of SC...

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Dades bibliogràfiques
Publicat a:Annu Int Conf IEEE Eng Med Biol Soc
Autors principals: Alambo, Amanuel, Andrew, Ryan, Gollarahalli, Sid, Vaughn, Jacqueline, Banerjee, Tanvi, Thirunarayan, Krishnaprasad, Abrams, Daniel, Shah, Nirmish
Format: Artigo
Idioma:Inglês
Publicat: 2020
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7545272/
https://ncbi.nlm.nih.gov/pubmed/33019301
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1109/EMBC44109.2020.9175599
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