Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Majid Shahabi
Hepcidin Gene Polymorphisms and Iron Overload in Β-Thalassemia Major Patients Refractory to Iron Chelating Therapy
BMC Medical Genetics
Genetics
Related publications
Glutathione S Transferase Polymorphisms Influence on Iron Overload in Β-Thalassemia Patients
Thalassemia Reports
Iron Chelating Agents for Iron Overload Diseases
Thalassemia Reports
Oxidative Stress and Iron Overload in Β-Thalassemia: An Overview
Quantitative Ultrasonic Analysis of Myocardium in Patients With Thalassemia Major and Iron Overload
Circulation
Cardiovascular Medicine
Physiology
Cardiology
Hepcidin Response to Acute Iron Intake and Chronic Iron Loading in Dysmetabolic Iron Overload Syndrome
Liver International
Hepatology
How Early Can Myocardial Iron Overload Occur in Beta Thalassemia Major?
PLoS ONE
Multidisciplinary
The Potential of Tin-Protoporphyrin as an Adjuvent Therapy for Iron Overload in Thalassemia Major
Pediatric Research
Child Health
Pediatrics
Perinatology
Right Ventricular Volumes and Function in Thalassemia Major Patients in the Absence of Myocardial Iron Overload
Journal of Cardiovascular Magnetic Resonance
Nuclear Medicine
Radiology
Ultrasound Technology
Cardiology
Family Practice
Radiological
Cardiovascular Medicine
Imaging
Myocardial Iron Overload in Sickle/Thalassemia Patients of Italian Origin
Journal of Cardiovascular Magnetic Resonance
Nuclear Medicine
Radiology
Ultrasound Technology
Cardiology
Family Practice
Radiological
Cardiovascular Medicine
Imaging