Coping Strategies in Patients with Beta-thalassemia and their Parents: A Systematic Review
Coping Strategies in Patients with Beta-thalassemia and their Parents: A Systematic Review

Bahareh Ahmadian; Monir Ramezani; Zahra Badiee; Saeed Vaghee

Volume 10, Issue 3 , March 2022, , Pages 15682-15694

https://doi.org/10.22038/ijp.2022.62544.4782

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
Transfusion Related Adverse Effects on Beta-Thalassemia Major and New Therapeutic Approaches: A Review Study

Saeed Dorgaleleh; Ahmad Barahouie; Karim Naghipoor; Farzad Dastaviz; Zahrasadat Ghodsalavi; Morteza Oladnabi

Volume 8, Issue 7 , July 2020, , Pages 11651-11661

https://doi.org/10.22038/ijp.2020.46749.3794

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
Quality of Life in Patients with Thalassemia Major: A Concept Analysis Using Rodgers' Evolutionary Method

Mahdieh Arian; Mohsen Soleimani; Ali Fakhr-Movahedi; Mohammad Bagher Oghazian; Zahra Badiee

Volume 8, Issue 5 , May 2020, , Pages 11197-11217

https://doi.org/10.22038/ijp.2019.42126.3547

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
Evaluation of the Efficacy of Lentiviral Vectors in Gene Therapy of Beta-thalassemia Patients: A Systematic Review

Saeed Dorgaleleh; Ahmad Barahouie; Farzad Dastaviz; Zahrasadat Ghodsalavi; Morteza Oladnabi

Volume 8, Issue 5 , May 2020, , Pages 11243-11250

https://doi.org/10.22038/ijp.2020.47309.3839

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
The Association between Dental Health Status and Oral Health-Related Quality of Life of Children Diagnosed with -Thalassemia Major in Zahedan City, Iran

Foroogh Amirabadi; Shirin Saravani; Ghasem Miri-Aliabad; Mahnaz Khorashadi-Zadeh

Volume 7, Issue 2 , February 2019, , Pages 8985-8991

https://doi.org/10.22038/ijp.2018.34517.3034

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
Regular Reminding of the Potential Serious Complications of Poor Adherence to Treatment: A Strategy for Improving Treatment Adherence in Beta-Thalassemia Major Patients

Amir Emami Zeydi; Abbas Heydari; Hossein Karimi Moonaghi

Volume 5, Issue 12 , December 2017, , Pages 6201-6202

https://doi.org/10.22038/ijp.2017.25718.2190

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
Diagnostic Value of NT-pro BNP Biomarker and Echocardiography in Cardiac Involvements in Beta-thalassemia Patients

Noor Mohammad Noori; Alireza Teimouri; Maryam Nakhaey Moghaddam

Volume 5, Issue 11 , November 2017, , Pages 6077-6094

https://doi.org/10.22038/ijp.2017.24951.2110

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
Evaluation of Dento-maxillofacial Changes in Pediatric ß-Thalassemia Major Patients in Northern Iran

Katayoun Salem; Maedeh Aminian; Samad Khamesi

Volume 5, Issue 7 , July 2017, , Pages 5219-5227

https://doi.org/10.22038/ijp.2017.22270.1862

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
Diagnostic Value of N Terminal Pro B Type Natriuretic Peptide (NT-pro BNP) in Cardiac Involvement in Patients with Beta- Thalassemia

Noor Mohammad Noori; Alireza Teimouri; Nahid Anvari

Volume 5, Issue 4 , April 2017, , Pages 4641-4662

https://doi.org/10.22038/ijp.2017.22370.1874

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
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

Mohammad Shooriabi; Azin Zareyee; Abdolreza Gilavand; Behzad Mansoori; Bijan Keykhaei Dehdezi

Volume 4, Issue 3 , March 2016, , Pages 1519-1527

https://doi.org/10.22038/ijp.2016.6595

Abstract
  Background: Thalassemia is the most common single-gene disorder that carries along many difficulties and effects such as oral and dental problems in patients. This study aimed to determine ...  Read More