Potential Effects of Silymarin and Its Flavonolignan Components in Patients with β-Thalassemia Major: A Comprehensive Review in 2015

Major β-thalassemia (β-TM) is one of the most common inherited hemolytic types of anemia which is caused as a result of absent or reduced synthesis of β-globin chains of hemoglobin. This defect results in red blood cells lysis and chronic anemia that can be treated by multiple blood transfusions and...

Descripción completa

Detalles Bibliográficos
Autores principales: Darvishi Khezri, Hadi, Salehifar, Ebrahim, Kosaryan, Mehrnoush, Aliasgharian, Aily, Jalali, Hossein, Hadian Amree, Arash
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779508/
https://www.ncbi.nlm.nih.gov/pubmed/26997953
http://dx.doi.org/10.1155/2016/3046373

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779508/
https://www.ncbi.nlm.nih.gov/pubmed/26997953
http://dx.doi.org/10.1155/2016/3046373

Ejemplares similares