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Hemoglobin
international journal for hemoglobin research
Volume 37, 2013 - Issue 5
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Original Article

Utility Of The Multivariate Approach In Predicting β-Thalassemia Intermedia Or β-Thalassemia Major Types In Iranian Patients

Mehdi BananGenetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, IranCorrespondence[email protected]
,
Hadi BayatGenetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
,
Pegah Namdar-AligoodarziGenetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
,
Azita AzarkeivanPediatric Hematology Oncology, Blood Transfusion Research Centre; High Institute for Research and Education in Transfusion Medicine; and Thalassemia Clinic, Tehran, Iran
,
Koorosh Kamali Department of Public Health, School of Public Health, Zanjan University of Medical Sciences, Zanjan, Iran
,
Parvaneh DaneshmandGenetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
,
Behzad Zaker-KandjaniGenetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
&
Hossein NajmabadiGenetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
 show all
Pages 413-422 | Received 12 Nov 2012, Accepted 23 Jan 2013, Published online: 27 Jun 2013

Citations (10)

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Read on this site (2)

Aumpika Kesornsit, Nutjaree Jeenduang, Dararat Horpet, Thunyaluk Plyduang & Manit Nuinoon. (2018) Quantitative Trait Loci Influencing Hb F Levels in Southern Thai Hb E (HBB: c.79G>A) Heterozygotes. Hemoglobin 42:1, pages 23-29.
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Behzad Zaker-Kandjani, Pegah Namdar-Aligoodarzi, Azita Azarkeivan, Hossein Najmabadi & Mehdi Banan. (2015) Mutation Screening of the Krüppel-Like Factor 1 Gene Using Single-Strand Conformational Polymorphism in a Cohort of Iranian β-Thalassemia Patients. Hemoglobin 39:1, pages 24-29.
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Articles from other publishers (8)

Mohammad Ali Sheikh Beig Goharrizi, Saeed Ghodsi & Mohammad Reza Memarjafari. (2023) Implications of CRISPR-Cas9 Genome Editing Methods in Atherosclerotic Cardiovascular Diseases. Current Problems in Cardiology 48:5, pages 101603.
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Saqib H. Ansari, Zeeshan Hussain, Muhammad Zohaib, Sadia Parveen, Bushra Kaleem, Hina Qamar, Omair Adil, Muhammad T. Khan & Tahir S. Shamsi. (2022) A Pragmatic Scoring Tool to Predict Hydroxyurea Response Among β-Thalassemia Major Patients in Pakistan. Journal of Pediatric Hematology/Oncology 44:1, pages e77-e83.
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Ali Dehshahri, Alessio Biagioni, Hadi Bayat, E. Hui Clarissa Lee, Mohammad Hashemabadi, Hojjat Samareh Fekri, Ali Zarrabi, Reza Mohammadinejad & Alan Prem Kumar. (2021) Editing SOX Genes by CRISPR-Cas: Current Insights and Future Perspectives. International Journal of Molecular Sciences 22:21, pages 11321.
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Mehdi Banan. (2020) Recent advances in CRISPR/Cas9-mediated knock-ins in mammalian cells. Journal of Biotechnology 308, pages 1-9.
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Hossein Jafari, Sara Hesami, Mojtaba Safi, Fatemeh Ghasemi & Mehdi Banan. (2019) Expression and hydroxyurea-triggered induction of EGFP upon CRISPR/Cas9-mediated integration into the γ-globin gene of K562 cells. Biotechnology Letters 41:6-7, pages 691-700.
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Nahal Maroofi, Azita Azarkeivan, Soosan Banihashemi, Saeid Mohammadparast, Ali Aghajanirefah & Mehdi Banan. (2017) An enhancer haplotype may influence BCL11A expression levels and the response to hydroxyurea in β-thalassemia patients . Pharmacogenomics 18:10, pages 995-967.
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Nasir A.S. Al-AllawiHelene PuehringerRuzaiqah A. RaheemChristian Oberkanins. (2015) Genetic Modifiers in β-Thalassemia Intermedia: A Study on 102 Iraqi Arab Patients. Genetic Testing and Molecular Biomarkers 19:5, pages 242-247.
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Mehdi Banan. (2013) Hydroxyurea treatment in β-thalassemia patients: to respond or not to respond?. Annals of Hematology 92:3, pages 289-299.
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