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)
Genetic Counseling for Families with Sporadic Intellectual Disability in North of Iran: A Retrospective Study
Genetic Counseling for Families with Sporadic Intellectual Disability in North of Iran: A Retrospective Study

Farzad Dastaviz; Mohammad Bagher Hashemi- Soteh; Peyman Aghabararian; Saeed Zareei; Saeed Dorgaleleh; Moosa Rajabi Vandchali; Mahsa Ghasempisheh; Morteza Oladnabi; Abouzar Bagheri

Volume 8, Issue 8 , August 2020, , Pages 11709-11718

https://doi.org/10.22038/ijp.2020.47310.3840

Abstract
  Background Intellectual Disability (ID) is a heterogeneous disorder, in which at least 600 genes participate. The present study aimed to identify the effect of genetic counseling and ...  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
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