Volume 12 (2024)
Volume 11 (2023)
Volume 10 (2022)
Volume 9 (2021)
Volume 8 (2020)
Volume 7 (2019)
Volume 6 (2018)
Volume 5 (2017)
Volume 4 (2016)
Volume 3 (2015)
Volume 2 (2014)
Volume 1 (2013)
Keywords = Beta-thalassemia
Number of Articles: 10
Coping Strategies in Patients with Beta-thalassemia and their Parents: A Systematic Review
Volume 10, Issue 3 , March 2022, , Pages 15682-15694
Abstract
Background: Thalassemia is one of the most common genetic disorders. Patients with thalassemia and their families face various challenges in their daily lives, which affect their coping ... Read More
Transfusion Related Adverse Effects on Beta-Thalassemia Major and New Therapeutic Approaches: A Review Study
Volume 8, Issue 7 , July 2020, , Pages 11651-11661
Abstract
Thalassemia is one of the most common genetic disorders, worldwide.Beta-Thalassemia Major (BTM) is the most severe type, which reduces lifeexpectancy and quality of life. In this study, ... Read More
Quality of Life in Patients with Thalassemia Major: A Concept Analysis Using Rodgers' Evolutionary Method
Volume 8, Issue 5 , May 2020, , Pages 11197-11217
Abstract
Background: Quality of life (QoL) is a complicated phenomenon in patients with thalassemia major. This study was conducted to clarify the concept of QoL in patients with thalassemia ... Read More
Evaluation of the Efficacy of Lentiviral Vectors in Gene Therapy of Beta-thalassemia Patients: A Systematic Review
Volume 8, Issue 5 , May 2020, , Pages 11243-11250
Abstract
Background Beta thalassemiais a genetic blood abnormality identified through mutations, which reduce the synthesis of the ß-globin chain. Gene therapy through Lentiviral vectors ... Read More
The Association between Dental Health Status and Oral Health-Related Quality of Life of Children Diagnosed with -Thalassemia Major in Zahedan City, Iran
Volume 7, Issue 2 , February 2019, , Pages 8985-8991
Abstract
Background: b-thalassemia major is a common hereditary blood disease that can affect patients’ oral health and quality of life. The present study aims to determine the relationship ... Read More
Regular Reminding of the Potential Serious Complications of Poor Adherence to Treatment: A Strategy for Improving Treatment Adherence in Beta-Thalassemia Major Patients
Volume 5, Issue 12 , December 2017, , Pages 6201-6202
Abstract
Globally, β-Thalassemia Major (β-TM) is the most commonly inherited hemolytic anemia, with a high incidence rate in Southeast Asia, the Middle East and Mediterranean countries. ... Read More
Diagnostic Value of NT-pro BNP Biomarker and Echocardiography in Cardiac Involvements in Beta-thalassemia Patients
Volume 5, Issue 11 , November 2017, , Pages 6077-6094
Abstract
Background N-terminal pro–B-type natriuretic peptide (NT-proBNP) is a marker to evaluate the cardiac involvement in thalassemia. We aimed to evaluate conventional and ... Read More
Evaluation of Dento-maxillofacial Changes in Pediatric ß-Thalassemia Major Patients in Northern Iran
Volume 5, Issue 7 , July 2017, , Pages 5219-5227
Abstract
Background Thalassemia is a group of congenital disorders which is characterized by a deficient synthesis of alfa or beta globulin chains in hemoglobin molecules. Due to the problems ... Read More
Diagnostic Value of N Terminal Pro B Type Natriuretic Peptide (NT-pro BNP) in Cardiac Involvement in Patients with Beta- Thalassemia
Volume 5, Issue 4 , April 2017, , Pages 4641-4662
Abstract
Background Heart failure is a major cause of death in thalassemia. The study aimed to determine the diagnostic value of N Terminal Pro B Type Natriuretic Peptide (NT-pro BNP), to early ... Read More
Investigating DMFT Indicator and its Correlation with the amount of Serum Ferritin and Hemoglobin in Students with Beta-thalassemia Major in Ahvaz, South West of Iran
Volume 4, Issue 3 , March 2016, , Pages 1519-1527