Arterial Stiffness and Endothelial Function in Patients with β-Thalassemia Major
Ahmed Emad El Din Mohammed Hassan;
Abstract
The thalassemias are heterogeneous group of genetic disorders of hemoglobin synthesis, all of which result from a reduced rate of production of one or more ofthe globin chains of hemoglobin. This basic defect results in imbalanced globin chain synthesis,
Other data
| Title | Arterial Stiffness and Endothelial Function in Patients with β-Thalassemia Major | Other Titles | تصلب الشرايين ومدى تأثر الخلايا المبطنة لجدار الوعاء الدموي فى مرضى أنيميا البحرالأبيض المتوسط | Authors | Ahmed Emad El Din Mohammed Hassan | Keywords | Arterial Stiffness and Endothelial Function in Patients with β-Thalassemia Major | Issue Date | 2011 | Description | The thalassemias are heterogeneous group of genetic disorders of hemoglobin synthesis, all of which result from a reduced rate of production of one or more ofthe globin chains of hemoglobin. This basic defect results in imbalanced globin chain synthesis, |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 106644p4041.pdf | 319.31 kB | Adobe PDF | View/Open |
Similar Items from Core Recommender Database
Items in Ain Shams Scholar are protected by copyright, with all rights reserved, unless otherwise indicated.