Therapeutic options and management approach on thalassemia an overview
HQ Mahmoud, RS Mhana, AA Mohammed - International Journal of …, 2024 - ijmsdh.org
People with thalassemia, the body produces an aberrant form of hemoglobin, a hereditary
blood condition that runs in families. Anemia is caused by this disorder, which causes a …
blood condition that runs in families. Anemia is caused by this disorder, which causes a …
Unveiling the molecular and comorbidity profile among transfusion-dependent and nontransfusion-dependent beta-thalassemic patients in Baghdad city
AA Alaqidi, HS Al-Mamoori - Iraqi Journal of Hematology, 2024 - journals.lww.com
BACKGROUND: Beta-thalassemia (BT) is the most common hereditary hemolytic disease in
Iraq. The high prevalence rate of this disorder, coupled with, frequently encountered severe …
Iraq. The high prevalence rate of this disorder, coupled with, frequently encountered severe …
[PDF][PDF] Association of the changes in hepatic enzymes, bilirubin, and plasma proteins with beta-thalassemia in iron over loaded-patients
GM Hussain, MA Abdullah, NY Hussein - academia.edu
Changes in liver enzymes and bilirubin in patients with thalassemia depend on genetic
changes and the association of other genetic determinants. Iron overload is associated with …
changes and the association of other genetic determinants. Iron overload is associated with …