Serum visfatin level in sickle/β thalassemia in correlation with frequency of vaso occlusion crises: A comparative study
Background: Hemoglobinopathies are the most common heritable disorders of erythrocytes, with sickle cell diseases (SCDs) and thalassemia being the most common. SCDs are characterized by the presence of sickle hemoglobin within red blood cell (RBC) as a result of point mutation (β6glu→val). SCDs incl...
Bewaard in:
| Hoofdauteurs: | , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Wolters Kluwer Medknow Publications
2022-01-01
|
| Reeks: | Medical Journal of Babylon |
| Onderwerpen: | |
| Online toegang: | http://www.medjbabylon.org/article.asp?issn=1812-156X;year=2022;volume=19;issue=1;spage=58;epage=65;aulast=Al-Jabory |
| Tags: |
Geen labels, Wees de eerste die dit record labelt!
|