Citations (97)
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Shaima Al-Zebari, Nasir AS Al-Allawi & Farida Nerweyi. (2023) Beta Globin Gene Cluster Haplotypes in Beta Thalassemia in the Kurdistan Region of Iraq. Hemoglobin 47:3, pages 111-117.
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Sulav D. Atroshi, Nasir A.S. Al-Allawi & Adil A. Eissa. (2021) Updated Molecular Spectrum of β-Thalassemia Mutations in Duhok Province, Northern Iraq: Ethnic Variation and the Impact of Immigration. Hemoglobin 45:4, pages 239-244.
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Milad Rafat, Zeinab Allamehzadeh, Mohammad Shekari, Masoumeh Afsa & Kianoosh Malekzadeh. (2021) The Effect of HBB: c.-121C>T Variant [–71 (C>T)] on the β-Globin Promoter: Case Series Study. Hemoglobin 45:4, pages 234-238.
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Azita Azarkeivan, Nader Cohan, Hamid Reza Niazkar, Arsalan Azizi & Fariba Rad. (2020) Hb S (HBB: c.20A>T) and α- and β-Thalassemia Coinheritance in Iranian Patients . Hemoglobin 44:2, pages 109-112.
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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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Sedat Yılmaz. (2019) The Spectrum of β-Thalassemia Mutations in Siirt Province, Southeastern Turkey. Hemoglobin 43:3, pages 174-181.
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Hossam Murad, Faten Moasses, Amir Dabboul, Yasser Mukhalalaty, Ahmad Omar Bakoor, Walid Al-Achkar & Rami A. Jarjour. (2018) Geographical distribution of β-globin gene mutations in Syria. Hematology 23:9, pages 697-704.
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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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Laudy Cherry, Carla Calo, Rodica Talmaci, Pascale Perrin & Lucian Gavrila. (2016) β-Thalassemia Haplotypes in Romania in the Context of Genetic Mixing in the Mediterranean Area. Hemoglobin 40:2, pages 85-96.
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Suha M. Hassan, Cornelis L. Harteveld, Egbert Bakker & Piero C. Giordano. (2015) Broader Spectrum of β-Thalassemia Mutations in Oman: Regional Distribution and Comparison with Neighboring Countries. Hemoglobin 39:2, pages 107-110.
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Rami A. Jarjour, Hossam Murad, Faten Moasses & Walid Al-Achkar. (2014) Molecular Update of β-Thalassemia Mutations in the Syrian Population: Identification of Rare β-Thalassemia Mutations. Hemoglobin 38:4, pages 272-276.
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Nima Hafezi-Nejad, Mohsen Khosravi, Nooshin Bayat, Ariana Kariminejad, Valeh Hadavi, Christian Oberkanins, Azita Azarkeivan & Hossein Najmabadi. (2014) Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience. Hemoglobin 38:3, pages 153-157.
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Hassan Joulaei, Mohammad Shahbazi, Bahman Nazemzadegan, Mohsen Rastgar, Maryam Hadibarhaghtalab, Mohammadreza Heydari, Fariborz Ghaffarpasand & Nazila Rahimi. (2014) The Diminishing Trend of β-Thalassemia in Southern Iran From 1997 to 2011: The Impact of Preventive Strategies. Hemoglobin 38:1, pages 19-23.
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Masomeh Mehrabi, Reza Alibakhshi, Soheila Fathollahi & Mohammad Reza Farshchi. (2013) The Spectrum of β-Thalassemia Mutations in Kermanshah Province in West Iran and its Association with Hematological Parameters. Hemoglobin 37:6, pages 544-552.
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Nasir A.S. Al-Allawi, Bassam M.S. Al-Mousawi, Ameer I.A. Badi & Sana D. Jalal. (2013) The Spectrum of β-Thalassemia Mutations in Baghdad, Central Iraq. Hemoglobin 37:5, pages 444-453.
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Ebrahim Miri-Moghaddam, Azita Zadeh-Vakili, Abbas Nikravesh, Shohreh Sanei Sistani & Mehrnaz Naroie-Nejad. (2013) Sistani Population: a Different Spectrum oF β-Thalassemia Mutations From other Ethnic Groups of Iran. Hemoglobin 37:2, pages 138-147.
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Nooshin Bayat, Samaneh Farashi, Nima Hafezi-Nejad, Negin Faramarzi, Mehri Ashki, Shadi Vakili, Hashem Imanian, Mohsen Khosravi, Azita Azar-Keivan & Hossein Najmabadi. (2013) Novel Mutations Responsible for α-Thalassemia in Iranian Families. Hemoglobin 37:2, pages 148-159.
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Ebrahim Miri-Moghaddam & Azita Zadeh-Vakili. (2012) Profile of β-Thalassemia and its Prenatal Diagnosis in Khorasan-E-Jonobi Province, Iran. Hemoglobin 36:5, pages 456-463.
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Hamid Galehdari, Bahaoddin Salehi, Somaiyeh Azmoun, Bijan Keikhaei, Khoda Morad Zandian & Mohammad Pedram. (2010) Comprehensive Spectrum of the β-Thalassemia Mutations in Khuzestan, Southwest Iran. Hemoglobin 34:5, pages 461-468.
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Sana D. Jalal, Nasir A.S. Al-Allawi, Nooshin Bayat, Hasham Imanian, Hossein Najmabadi & Azad Faraj. (2010) β-Thalassemia Mutations in the Kurdish Population of Northeastern Iraq. Hemoglobin 34:5, pages 469-476.
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Roshan Colah, Ajit Gorakshakar & Anita Nadkarni. (2010) Global burden, distribution and prevention of β-thalassemias and hemoglobin E disorders. Expert Review of Hematology 3:1, pages 103-117.
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Rasoul Salehi, Christopher A. Fisher, Patricia A. Bignell, Gilda Eslami & John M. Old. (2010) Identification of Three Novel Mutations [−41 (A>C), codon 24 (–G), and IVS-I-109 (−T)], in a Study of β-Thalassemia Alleles in the Isfahan Region of Iran. Hemoglobin 34:1, pages 115-120.
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Azita Zadeh-Vakili & Payman Eshghi. (2009) Detection of a Rare Mutation in An Iranian Family: Codons 37/38/39 (7 bp Deletion). Hemoglobin 33:6, pages 523-527.
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Nasrollah Saleh-Gohari & Arezu Khosravi Mashizi. (2009) A Family with the 619 bp Deletion on the β-globin Gene Found in Kerman Province, Iran. Hemoglobin 33:6, pages 515-518.
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Mohammad Ali Ehsani, Amir Abbas Hedayati-Asl, Alireza Bagheri, Syrus Zeinali & Armin Rashidi. (2009) HYDROXYUREA-INDUCED HEMATOLOGICAL RESPONSE IN TRANSFUSION-INDEPENDENT BETA-THALASSEMIA INTERMEDIA: Case Series and Review of Literature. Pediatric Hematology and Oncology 26:8, pages 560-565.
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Valeh Hadavi, Maryam Jafroodi, Nima Hafezi-Nejad, Sousan Dehnadi Moghadam, Fatemeh Eskandari, Shahin Tarashohi, Hamideh Pourfahim, Christian Oberkanins, Hai-Yang Law & Hossein Najmabadi. (2009) α-Thalassemia Mutations in Gilan Province, North Iran. Hemoglobin 33:3-4, pages 235-241.
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Mehdi Haghi, Abbas Ali Hosseinpour Feizi, Mohammad Ali Hosseinpour Feizi, Nasser Pouladi & A. Nazli Başak. (2009) Is the Frameshift Codons 8/9 (+G) [FSC 8/9 (+G)] β-Thalassemia Mutation, Detected by the Polymerase Chain Reaction-Amplification Refractory Mutation System, Really FSC 8/9 (+G)?. Hemoglobin 33:3-4, pages 279-282.
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Mehdi Haghi, Shohre Khorshidi, Mohammad Ali Hosseinpour Feizi, Nasser Pouladi & Abbas A. Hosseinpour Feizi. (2009) β-Thalassemia Mutations in the Iranian Kurdish Population of Kurdistan and West Azerbaijan Provinces. Hemoglobin 33:2, pages 109-114.
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Khodamorad Zandian, Jamal Nateghi, Bijan Keikhaie, Mohammad Pedram, Nima Hafezi-Nejad, Valeh Hadavi, Christian Oberkanins, Azita Azarkeivan, Hai-Yang Law & Hossein Najmabadi. (2008) α-Thalassemia Mutations in Khuzestan Province, Southwest Iran. Hemoglobin 32:6, pages 546-552.
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Pooneh Nikuei, Valeh Hadavi, Minoo Rajaei, Mozhgan Saberi, Fozieh Hajizade & Hossein Najmabadi. (2008) Prenatal Diagnosis for β-Thalassemia Major in the Iranian Province of Hormozgan. Hemoglobin 32:6, pages 539-545.
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Peyman Eshghi, Armin Rashidi, Azita Zadeh-Vakili & Ebrahim Miri-Moghadam. (2008) Hematological Phenotype of the IVS-I-5 (G > C) β-Thalassemia Mutation and Assessment of Iran's National Screening Criteria. Hemoglobin 32:5, pages 440-445.
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Mohammad A. Hosseinpour Feizi, Abbas A. Hosseinpour Feizi, Nasser Pouladi, Mehdi Haghi & Parvin Azarfam. (2008) Molecular Spectrum of β-Thalassemia Mutations in Northwestern Iran. Hemoglobin 32:3, pages 255-261.
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Peyman Eshghi, Azita Zadeh-Vakili, Armin Rashidi & Ebrahim Miri-Moghadam. (2008) An Unusually Frequent β-Thalassemia Mutation in an Iranian Province. Hemoglobin 32:4, pages 387-392.
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Fatemehsadat Esteghamat, Hashem Imanian, Azita Azarkeivan, Farzin Pourfarzad, Navid Almadani & Hossein Najmabadi. (2007) Screening of Iranian Thalassemic Families for the Most Common Deletions of the β-Globin Gene Cluster. Hemoglobin 31:4, pages 463-469.
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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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Pupak Derakhshandeh-Peykar, Haleh Akhavan-Niaki, Ahmad Tamaddoni, Shohreh Ghawidel-Parsa, Kourosh Holakouie Naieni, Manijeh Rahmani, Farbod Babrzadeh, Mohammad Dilmaghani-Zadeh & Dariush Daneshvar Farhud. (2007) Distribution of β-Thalassemia Mutations in the Northern Provinces of Iran. Hemoglobin 31:3, pages 351-356.
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Ali Asghar Kiani, Yousef Mortazavi, Sirous Zeinali & Yaghob Shirkhani. (2007) The Molecular Analysis of β-Thalassemia Mutations in Lorestan Province, Iran. Hemoglobin 31:3, pages 343-349.
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Aisha Al-Obaidli, Mowafak Hamodat, Zainab Fawzi, Mohamed Abu-Laban, Nathalie Gerard & Rajagopal Krishnamoorthy. (2007) Molecular Basis of Thalassemia in Qatar. Hemoglobin 31:2, pages 121-127.
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Nasir A.S. Al-Allawi, Jalaldet M.S. Jubrael & Michael Hughson. (2006) Molecular Characterization of β-Thalassemia in the Dohuk Region of Iraq. Hemoglobin 30:4, pages 479-486.
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Mardawig Alebouyeh. (2005) PEDIATRIC HEMATOLOGY AND ONCOLOGY IN IRAN. Pediatric Hematology and Oncology 22:1, pages 1-9.
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Babak Moghimi, Majid Yavarian, Christian Oberkanins, Seyyed Saeid Hosseini Amini, Shohreh Khatami, Soghra Rouhi, Kimia Kahrizi & Hossein Najmabadi. (2004) Hb Dhonburi (Neapolis) [β126(H4)Val→Gly] Identified in a Family from Northern Iran. Hemoglobin 28:4, pages 353-356.
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Maryam Neishabury, Christian Oberkanins, Lia Abbasi Moheb, Ali Akbar Pourfathollah, Kimia Kahrizi, Elahe Keyhany, Walter Krugluger & Hossein Najmabadi. (2003) High Prevalence of the −α3.7 Deletion Among Thalassemia Patients in Iran. Hemoglobin 27:1, pages 53-55.
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Mehran Karimi, Hooman Yarmohammadi, Shirin Farjadian, Sirus Zeinali, Zahra Moghaddam, Maria D. Cappellini & Piero C. Giordano. (2002) β-THALASSEMIA INTERMEDIA FROM SOUTHERN IRAN: IVS-II-1 (G→A) IS THE PREVALENT THALASSEMIA INTERMEDIA ALLELE. Hemoglobin 26:2, pages 147-154.
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Articles from other publishers (54)
Ekta Rao, Sandip Kumar Chandraker, Mable Misha Singh & Ravindra Kumar. (2024) Global distribution of β-thalassemia mutations: An update. Gene 896, pages 148022.
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Shahram Sedghi & Somayeh Ghaffari Heshajin. (2023) Citation analysis and mapping of genetics research in Iran. Global Knowledge, Memory and Communication.
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F.H. Abbasali, K.Sh. Mahmoud, N. Hengameh, D.H. Mina, D. Setare, D.M Hale & D.M. Sima. (2023) Rare and New Mutations of B-Globin in Azari Population of Iran, a Considerable Diversity. Balkan Journal of Medical Genetics 25:2, pages 51-62.
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Yeganeh Keshvar, Solmaz Sabeghi, Zohreh Sharifi, Kiyana Sadat Fatemi, Panti Fouladi, Shahrzad Younesi Khah, Faezeh Rahiminejad, Atefeh Joudaki, Masoume Amini, Hamideh Bagherian, Marefat Ghaffari Novin, Mansoureh Movahedin, Marzieh Mojbafan & Sirous Zeinali. (2022) A decade of molecular preimplantation genetic diagnosis of 350 blastomeres for beta-thalassemia combined with HLA typing, aneuploidy screening and sex selection in Iran. BMC Pregnancy and Childbirth 22:1.
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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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Anoushka Adler, Tamar Wainstock & Eyal Sheiner. (2021) Prenatal exposure to maternal β-thalassemia minor and the risk for long-term hematologic morbidity in the offspring: A population-based cohort study. Early Human Development 158, pages 105397.
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Hamid Galehdari, Mehdi Bijanzadeh, Seyedeh Zohreh Azarshin, Mohammad Shafee & Sogand Heydaran. (2021) Design and Development of Reverse Slot Blot for the Simultaneous Detection of Rare and Regional Specific Mutations in the Beta Globin Gene in Khuzestan Province of Iran. Indian Journal of Hematology and Blood Transfusion 37:3, pages 436-441.
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Ahmet Kursad Gunes & Hilmi Erdem Gozden. (2021) The Spectrum of Beta-Thalassemia Mutations in Syrian Refugees and Turkish Citizens. Cureus.
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Abdullah Arpaci, Bahar Unlu Gul, Oguzhan Ozcan, Gul Ilhan, Cigdem El, Emre Dirican, Sibel Elmacioglu & Hasan Kaya. (2021) Presentation of two new mutations in the 3′untranslated region of the β-globin gene and evaluating the molecular spectrum of thalassemia mutations in the Mediterranean region of Turkey. Annals of Hematology 100:6, pages 1429-1438.
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Nasir Al-Allawi, Sarah Al Allawi & Sana D. Jalal. (2020) Genetic epidemiology of hemoglobinopathies among Iraqi Kurds. Journal of Community Genetics 12:1, pages 5-14.
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Parinaz Zarghamian, Azita Azarkeivan, Ali Arabkhazaeli, Ahmad Mardani & Majid Shahabi. (2020) Hepcidin gene polymorphisms and iron overload in β-thalassemia major patients refractory to iron chelating therapy. BMC Medical Genetics 21:1.
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Ketki Kelkar, Vijay Ramanan, Siddharth Anand, Purvi Majethia, Shatakshi Ranade, Kunal Patil, Priyanka Gangodkar, Ashwini Bapat, Asawari Pilankar, Vidula Sengaokar, Kavita Khatod, Meenal Agarwal & Nikhil Phadke. (2020) HBB gene mutation spectrum in an Indian cohort of 1530 cases using an in-house targeted next-generation sequencing assay. Journal of Hematopathology 13:4, pages 239-248.
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Gunay Aliyeva, Chingiz Asadov, Tahira Mammadova, Surmaya Gafarova, Yegana Guliyeva & Eldar Abdulalimov. (2019) Molecular and geographical heterogeneity of hemoglobinopathy mutations in Azerbaijanian populations. Annals of Human Genetics 84:3, pages 249-258.
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Seyed Mohammad Bagher Hashemi‐Soteh, Hossein Karami, Seyed Saeid Mousavi, Touraj Farazmandfar & Ahmad Tamadoni. (2019) Alpha‐globin gene mutation spectrum in patients with microcytic hypochromic anemia from Mazandaran Province, Iran. Journal of Clinical Laboratory Analysis 34:1.
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Furqan Muein Auda, Afrodet A. Saleh & Dawood Salman Ali. (2019) The frequency of 6 beta-thalassemia mutations in the Iraqi patients from Najaf province. Gene Reports 17, pages 100516.
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Zohreh Mehrjoo, Zohreh Fattahi, Maryam Beheshtian, Marzieh Mohseni, Hossein Poustchi, Fariba Ardalani, Khadijeh Jalalvand, Sanaz Arzhangi, Zahra Mohammadi, Shahrouz Khoshbakht, Farid Najafi, Pooneh Nikuei, Mohammad Haddadi, Elham Zohrehvand, Morteza Oladnabi, Akbar Mohammadzadeh, Mandana Hadi Jafari, Tara Akhtarkhavari, Ehsan Shamsi Gooshki, Aliakbar Haghdoost, Reza Najafipour, Lisa-Marie Niestroj, Barbara Helwing, Yasmina Gossmann, Mohammad Reza Toliat, Reza Malekzadeh, Peter Nürnberg, Kimia Kahrizi, Hossein Najmabadi & Michael Nothnagel. (2019) Distinct genetic variation and heterogeneity of the Iranian population. PLOS Genetics 15:9, pages e1008385.
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Gunay Aliyeva, Chingiz Asadov, Tahira Mammadova, Surmaya Gafarova & Eldar Abdulalimov. (2018) Thalassemia in the laboratory: pearls, pitfalls, and promises. Clinical Chemistry and Laboratory Medicine (CCLM) 57:2, pages 165-174.
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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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Ahmad N. Hasan & Mustafa S. Al-Attar. Molecular investigations of β-thalassemic children in Erbil governorate. Molecular investigations of β-thalassemic children in Erbil governorate.
MARYAM BEHESHTIAN, NASIM IZADI, GERNOT KRIEGSHAUSER, KIMIA KAHRIZI, ELHAM PARSI MEHR, MARYAM ROSTAMI, MASOUMEH HOSSEINI, MARYAM AZAD, MONA MONTAJABINIAT, ARIANA KARIMINEJAD, STEFAN NEMETH, CHRISTIAN OBERKANINS & HOSSEIN NAJMABADI. (2016) Prevalence of common MEFV mutations and carrier frequencies in a large cohort of Iranian populations. Journal of Genetics 95:3, pages 667-674.
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Ali Bazi, Ebrahim Miri-Moghaddam & Zahra Moudi. (2016) The High Birth Rate of Thalassemia Major and the Associated Problems in Sistan and Baluchistan Province, Iran. Gene, Cell and Tissue 3:4.
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J. F. Borgio, S. AbdulAzeez, Z. A. Naserullah, S. Al‐Jarrash, R. A. Al‐Ali, M. S. Al‐Madan, F. Al‐Muhanna, A. M. Al‐Suliman, A. Al‐Nafie, M. H. Steinberg & A. K. Al‐Ali. (2016) Mutations in the β‐globin gene from a Saudi population: an update. International Journal of Laboratory Hematology 38:2.
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Gaurav Thareja, Sumi Elsa John, Prashantha Hebbar, Kazem Behbehani, Thangavel Alphonse Thanaraj & Osama Alsmadi. (2015) Sequence and analysis of a whole genome from Kuwaiti population subgroup of Persian ancestry. BMC Genomics 16:1.
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Adil A. Eissa, Muna A. Kashmoola, Sulav D. Atroshi & Nasir A. S. Al-Allawi. (2014) Molecular Characterization of β-Thalassemia in Nineveh Province Illustrates the Relative Heterogeneity of Mutation Distributions in Northern Iraq. Indian Journal of Hematology and Blood Transfusion 31:2, pages 213-217.
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J. Francis Borgio, S. AbdulAzeez, Awatif N. Al-Nafie, Zaki A. Naserullah, Sana Al-Jarrash, Mohammed S. Al-Madan, Fahad Al-Muhanna, Martin H. Steinberg & Amein K. Al-Ali. (2014) A novel HBA2 gene conversion in cis or trans: “α12 allele” in a Saudi population. Blood Cells, Molecules, and Diseases 53:4, pages 199-203.
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Mohammad Amin Honardoost, Hosein Tabatabaeian, Mojtaba Akbari & Mansoor Salehi. (2014) Investigation of sensitivity, specificity and accuracy of Tetra primer ARMS PCR method in comparison with conventional ARMS PCR, based on sequencing technique outcomes in IVS-II-I genotyping of beta thalassemia patients. Gene 549:1, pages 1-6.
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Hengameh Nasouhipur, Ali Banihashemi, Reza Youssefi Kamangar & Haleh Akhavan-Niaki. (2014) Hb Knossos: HBB:c.82G>T Associated with HBB:c.315+1G>A Beta Zero Mutation Causes Thalassemia Intermedia. Indian Journal of Hematology and Blood Transfusion 30:S1, pages 243-245.
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A. H. M. AL-Faisal, I. J. AL-Ramahi, I. A. Abudl-Hassan, A. T. Hamdan & S. Barusrux. (2012) Detection of heterozygous c.1708C>T and c.1978C>G thyroid peroxidase (TPO) mutations in Iraqi patients with toxic and nontoxic goiter. Comparative Clinical Pathology 23:1, pages 69-75.
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Maryam Neishabury, Fahimeh Zamani, Elahe Keyhani, Azita Azarkeivan, Seyedeh Sedigheh Abedini, Masumeh Sadat Eslami, Setareh Talebi Kakroodi, Mahjoobeh Jafari Vesiehsari & Hossein Najmabadi. (2013) The influence of the BCL11A polymorphism on the phenotype of patients with beta thalassemia could be affected by the beta globin locus control region and/or the Xmn1-HBG2 genotypic background. Blood Cells, Molecules, and Diseases 51:2, pages 80-84.
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Hanan A. Hamamy & Nasir A. S. Al-Allawi. (2012) Epidemiological profile of common haemoglobinopathies in Arab countries. Journal of Community Genetics 4:2, pages 147-167.
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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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M. Rashid & M. Karimi. (2011) Compliance of deferoxamine injection in beta‐thalassaemia major patients in Iran. Transfusion Medicine 22:2, pages 104-107.
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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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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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E. Miri‐Moghaddam, A. Zadeh‐Vakili, Z. Rouhani, M. Naderi, P. Eshghi & A. Khazaei Feizabad. (2011) Molecular basis and prenatal diagnosis of β‐thalassemia among Balouch population in Iran. Prenatal Diagnosis 31:8, pages 788-791.
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Haleh Akhavan-NiakiSiamak Shafiezadeh SerestiBeheshteh AsghariAli Banihashemi. (2011) IVSII-666 of Human Beta-Globin Gene: A Polymorphic Marker Linked to Codon 8(-AA) Mutation. Genetic Testing and Molecular Biomarkers 15:7-8, pages 573-576.
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Haleh Akhavan-Niaki, Poupak Derakhshandeh-Peykar, Ali Banihashemi, Amrollah Mostafazadeh, Beheshteh Asghari, Mohammad-Reza Ahmadifard, Mandana Azizi, Ali Youssefi & Maryam Mitra Elmi. (2011) A comprehensive molecular characterization of beta thalassemia in a highly heterogeneous population. Blood Cells, Molecules, and Diseases 47:1, pages 29-32.
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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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Muhammad UsmanMoinuddin MoinuddinSyed Azhar Ahmed. (2011) Role of iron deficiency anemia in the propagation of beta thalssemia gene. The Korean Journal of Hematology 46:1, pages 41.
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Nasir A. S. Al-Allawi, Kawa M. A. Hassan, Anwar K. Sheikha, Farida F. Nerweiy, Raji S. Dawood & Jaladet Jubrael. (2010) -Thalassemia Mutations among Transfusion-Dependent Thalassemia Major Patients in Northern Iraq. Molecular Biology International 2010, pages 1-4.
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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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M. Hasanzad, M. Azad, K. Kahrizi, B. S. Saffar, S. Nafisi, Z. Keyhanidoust, M. Azimian, A. A. Refah, E. Also, J. A. Urtizberea, E. F. Tizzano & H. Najmabadi. (2009) Carrier frequency of SMA by quantitative analysis of the SMN1 deletion in the Iranian population. European Journal of Neurology 17:1, pages 160-162.
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Mehran Karimi, Rahil Giti, Sezaneh Haghpanah, Azita Azarkeivan, Hamid Hoofar & Masoomeh Eslami. (2009) Malignancies in patients with β‐thalassemia major and β‐thalassemia intermedia: A multicenter study in Iran. Pediatric Blood & Cancer 53:6, pages 1064-1067.
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