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Zahra Sajadpour, Zeinab Amini-Farsani, Majid Motovali-Bashi, Mitra Yadollahi & Nariman Khosravi-Farsani. (2020) Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran. Hemoglobin 44:1, pages 27-30.
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Ebrahim Miri-Moghaddam, Sara Bahrami, Majid Naderi, Ali Bazi & Morteza Karimipoor. (2016) Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran. Hemoglobin 40:3, pages 173-178.
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Mehdi Banan, Hadi Bayat, Pegah Namdar-Aligoodarzi, Azita Azarkeivan, Koorosh Kamali, Parvaneh Daneshmand, Behzad Zaker-Kandjani & Hossein Najmabadi. (2013) Utility Of The Multivariate Approach In Predicting β-Thalassemia Intermedia Or β-Thalassemia Major Types In Iranian Patients. Hemoglobin 37:5, pages 413-422.
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Mehdi Banan, Hadi Bayat, Azita Azarkeivan, Saeid Mohammadparast, Koorosh Kamali, Samaneh Farashi, Nooshin Bayat, Masumeh Hadavand Khani, Maryam Neishabury & Hossein Najmabadi. (2012) The XmnI and BCL11A Single Nucleotide Polymorphisms May Help Predict Hydroxyurea Response in Iranian β-Thalassemia Patients. Hemoglobin 36:4, pages 371-380.
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Amel Haj Khelil, Sabri Denden, Nadia Leban, Houria Daimi, Ramzi Lakhdhar, Gérard Lefranc, Jemni Ben Chibani & Pascale Perrin. (2010) Hemoglobinopathies in North Africa: A Review. Hemoglobin 34:1, pages 1-23.
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Mohammad Hamid, Frouzandeh Mahjoubi, Mohammad T. Akbari, Aida Arab, Sirous Zeinali & Morteza Karimipoor. (2009) Molecular Analysis of γ-Globin Promoters, HS-111 and 3′HS1, in β-thalassemia Intermedia Patients Associated with High Levels of Hb F. Hemoglobin 33:6, pages 428-438.
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Ishwar C. Verma, Marina Kleanthous, Renu Saxena, Suthat Fucharoen, Pranee Winichagoon, Sheikh Raizuddin, Shaheen N. Khan, Mohammad T. Akbari, Mina Izadyar, Navratnam Kotea, John M. Old, Panayiotis A. Ioannou & Baldip Khan. (2007) Multicenter Study of the Molecular Basis of Thalassemia Intermedia in Different Ethnic Populations. Hemoglobin 31:4, pages 439-452.
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S. Mohammad Eram, Babak Azimifar, Hassan Abolghasemi, Panty Foulady, Vida Lotfi, Maryam Masrouri, Maesomeh Hosseini, Afsaneh Abdolhosseini & Sirous Zeinali. (2005) The IVS-II-1 (G → A) β0-Thalassemia Mutation in CIS with Hb A2-Troodos [δ116(G18)Arg → Cys (CGC → TGC)] Causes a Complex Prenatal Diagnosis in an Iranian Family. Hemoglobin 29:4, pages 289-292.
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Articles from other publishers (24)
Anousheh Shasttiri, Misagh Moridi, Abbas Safari, Sayed Haidar Abbas Raza, Mostafa Ghaderi-Zefrehei, Massoud Houshmand, Ahmad Oryan, Mohammad Hossein Sanati, Jacqueline Smith & Motahareh Amjadi. (2021) Following the Trace of HVS II Mitochondrial Region Within the Nine Iranian Ethnic Groups Based on Genetic Population Analysis. Biochemical Genetics 60:3, pages 987-1006.
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Rashail Faraon, Mahmoud Daraghmah, Fekri Samarah & Mahmoud A. Srour. (2019) Molecular characterization of β-thalassemia intermedia in the West Bank, Palestine. BMC Hematology 19:1.
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Saqib Ansari, Nabil Rashid, Anny Hanifa, Saima Siddiqui, Bushra Kaleem, Arshi Naz, Kousar Perveen, Zeeshan Hussain, Iqra Ansari, Qammar Jabbar, Tahir Khan, Muhammad Nadeem & Tahir Shamsi. (2019) Laboratory diagnosis for thalassemia intermedia: Are we there yet?. Journal of Clinical Laboratory Analysis 33:1, pages e22647.
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Masoomeh Sayahi, Farideh Ghanbari Mardasi & Masoomeh Salehi Kambo. (2017) Thalassemia Spectrum and Prenatal Diagnosis among Voluntary Couples in Shushtar City, during a Five Year Period. Gene, Cell and Tissue 4:4.
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Nadir Ali, Muhammad Ayyub, Saleem Ahmed Khan, Suhaib Ahmed, Kazim Abbas, Hamid Saeed Malik & Sunila Tashfeen. (2015) Frequency of Gγ-globin promoter −158 (C>T) XmnI polymorphism in patients with homozygous/compound heterozygous beta thalassaemia. Hematology/Oncology and Stem Cell Therapy 8:1, pages 10-15.
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Ravindra Kumar, Anupriya Kaur & Sarita Agarwal. (2013) Influence of Xmn 1Gγ (HBG2 c.-211 C → T) Globin Gene Polymorphism on Phenotype of Thalassemia Patients of North India. Indian Journal of Hematology and Blood Transfusion 30:4, pages 286-290.
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Zohreh Rahimi. (2013) Genetic Epidemiology, Hematological and Clinical Features of Hemoglobinopathies in Iran. BioMed Research International 2013, pages 1-10.
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Rabah M. Shawky & Tarek M. Kamal. (2012) Thalassemia intermedia: An overview. Egyptian Journal of Medical Human Genetics 13:3, pages 245-255.
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Mohammadreza Bordbar, Sezaneh Haghpanah, Abdolreza Afrasiabi, Javad Dehbozorgian & Mehran Karimi. (2012) Genotype–phenotype correlation related to lipid profile in beta-thalassemia major and intermedia in southern Iran. Journal of Clinical Lipidology 6:2, pages 108-113.
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Gururaj D. KulkarniSuyamindra S. KulkarniGurushantappa S. KadakolBhushan B. KulkarniPrakashgouda H. KyamangoudarBhaskar V.K.S. LakkakulaKumarasamy ThangarajTipperudra A. ShepurMuralidhar L. KulkarniPramod B. Gai. (2012) Molecular Basis of β-Thalassemia in Karnataka, India. Genetic Testing and Molecular Biomarkers 16:2, pages 138-141.
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Ali Reza Rezaee, Mohammad Mehdi Banoei, Elham Khalili & Massoud Houshmand. (2012) Beta-Thalassemia in Iran: New Insight into the Role of Genetic Admixture and Migration. The Scientific World Journal 2012, pages 1-7.
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Aida Arab, Morteza Karimipoor, Ali Rajabi, Mohammad Hamid, Sedeigheh Arjmandi & Sirous Zeinali. (2010) Molecular characterization of β-thalassemia intermedia: a report from Iran. Molecular Biology Reports 38:7, pages 4321-4326.
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Maryam Neishabury, Azita Azarkeivan, Christian Oberkanins, Seyedeh Sedigheh Abedini, Shahbaz Zamani & Hossein Najmabadi. (2011) Analyzing 5′HS3 and 5′HS4 LCR core regions and NF-E2 in Iranian thalassemia intermedia patients with normal or carrier status for beta-globin mutations. Blood Cells, Molecules, and Diseases 46:3, pages 201-205.
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Maryam Neishabury, Azita Azarkeivan & Hossein Najmabadi. (2010) Frequency of Positive XmnI Gγ polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutation. Blood Cells, Molecules, and Diseases 44:2, pages 95-99.
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Hooshang Nemati, Zohreh Rahimi & Gholamreza Bahrami. (2009) The Xmn1 polymorphic site 5′ to the Gγ gene and its correlation to the Gγ:Aγ ratio, age at first blood transfusion and clinical features in β-Thalassemia patients from Western Iran. Molecular Biology Reports 37:1, pages 159-164.
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Zohreh Rahimi, Adriana Muniz & Abbas Parsian. (2009) Detection of responsible mutations for beta thalassemia in the Kermanshah Province of Iran using PCR-based techniques. Molecular Biology Reports 37:1, pages 149-154.
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Mehran Karimi, Majid Yavarian, Abdolreza Afrasiabi, Javad Dehbozorgian & Eliezer Rachmilewitz. (2008) Prevalence of β-Thalassemia Trait and Glucose-6-Phosphate Dehydrogenase Deficiency in Iranian Jews. Archives of Medical Research 39:2, pages 212-214.
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Mehran Karimi, Maryam Khanlari & Eliezer A. Rachmilewitz. (2007) Cerebrovascular accident in β‐thalassemia major (β‐TM) and β‐thalassemia intermedia (β‐TI). American Journal of Hematology 83:1, pages 77-79.
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H. Ansari, H. Kamani & A. Arbabi Sarjo. (2007) Prevalence of Hepatitis C and Related Factors among Beta-Thalassemia Major Patients in Southern Iran in 2005-2006. Journal of Medical Sciences 7:6, pages 997-1002.
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Shahram Akhlaghpoor. (2006) Chorionic villus sampling for beta-thalassemia: the first report of experience in Iran. Prenatal Diagnosis 26:12, pages 1131-1136.
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Roshan Colah, Anita Nadkarni, Ajit Gorakshakar, Supriya Phanasgaonkar, Reema Surve, P.G. Subramaniam, Nagnath Bondge, Kamala Pujari, Kanjaksha Ghosh & Dipika Mohanty. (2004) Impact of β globin gene mutations on the clinical phenotype of β thalassemia in India. Blood Cells, Molecules, and Diseases 33:2, pages 153-157.
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