Physiological study for some blood parameters in patients with major β-Thalassemia in Sulaymaniyah, Kurdistan, Iraq.
FF Rija - Tikrit Medical Journal, 2016 - search.ebscohost.com
Abstract β-thalassemia is an inherited hemolytic disorder caused by partial or complete
deficiency of a or β-globin chain synthesis. The disease leads to serious health problems …
deficiency of a or β-globin chain synthesis. The disease leads to serious health problems …
[PDF][PDF] HEMATOLOGICAL STUDY OF SOME BLOOD PARAMETERS IN PATIENT WITH MAJOR β-THALASSEMIA
FSA Alwan - Plant Archives, 2021 - plantarchives.org
Thalassemia is the most important diseases of hemolytic anemia, and it is a Greek word
originally that means Mediterranean anemia, this disease was known and resounded in this …
originally that means Mediterranean anemia, this disease was known and resounded in this …
[PDF][PDF] Department of Biology, Education college for pure Sceince, University of Karbala
AK Abeid - Journal of Kerbala University, 2014 - iasj.net
β-Thalassemia is more an inherted anemia publicity that common in the world and
especially in Mediterranean region, and the most important cause of mortality in patients …
especially in Mediterranean region, and the most important cause of mortality in patients …
[引用][C] Physiological study for some blood parameters in children with major B-Thalassemia in Al-Najaf governorate/Iraq.
A Kadhem Abeid - journal of kerbala university, 2014 - Kerbala University