Citations (26)
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Hossam Murad, Faten Moassas, Bouthina Ali, Eiad Katranji & Yasser Mukhalalaty. (2023) The Spectrum of α-Thalassemia Mutations in Syrian Patients. Hemoglobin 47:6, pages 245-248.
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Keivan Moradi, Mozaffar Aznab, Azam Azimi, Mostafa Biglari, Samaneh Shafieenia & Reza Alibakhshi. (2022) α-Thalassemia Mutations in Ilam Province, West Iran. Hemoglobin 46:3, pages 147-152.
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Mina Ebrahimi, Javad Mohammadi-Asl & Fakher Rahim. (2021) The worldwide molecular spectrum and distribution of thalassaemia: a systematic review. Annals of Human Biology 48:4, pages 307-312.
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Sara Alimohammadi-Bidhendi, Sarah Azadmehr, Masoumeh Razipour, Sirous Zeinali, Maryam Eslami & Elham Davoudi-Dehaghani. (2021) Regulatory Mutation Study in Cases with Unsolved Hypochromic Microcytic Anemia and α-Major Regulatory Element Haplotype Analysis in Iran. Hemoglobin 45:1, pages 37-40.
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Keivan Moradi, Mozaffar Aznab, Mostafa Biglari, Samaneh Shafieenia, Azam Azimi, Nushin Bijari & Reza Alibakhshi. (2020) Molecular Genetic Analysis of α-Thalassemia in Hamadan Province, West Iran. Hemoglobin 44:5, pages 319-324.
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Arwa Z. Al-Riyami, Shahina Daar, Salam Al Kindi, Ali Al Madhani, Yasser Wali, Mohammed Al Rawahi & Shoaib Al Zadjali. (2020) α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region. Hemoglobin 44:1, pages 20-26.
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Qiang Zhang, Xin Fan, Mingli Xu, Yijia Zhang, Huiling Xu, Xiaojun Wen & Wanjun Zhou. (2017) Hb H Disease Caused by Multiple Mutations in the Polyadenylation Signal Site and − −SEA/αα. Hemoglobin 41:3, pages 189-192.
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Hajar Eftekhari, Ahmad Tamaddoni, Hassan Mahmoudi Nesheli, Mohsen Vakili, Sadegh Sedaghat, Ali Banihashemi, Mandana Azizi, Reza Youssefi Kamangar & Haleh Akhavan-Niaki. (2017) A Comprehensive Molecular Investigation of α-Thalassemia in an Iranian Cohort from Different Provinces of North Iran. Hemoglobin 41:1, pages 32-37.
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Sima M. Derakhshan, Mahmoud S. Khaniani, Fateme Afkhami & Abbasali H. PourFeizi. (2016) Molecular Study of Deletional and Nondeletional Mutations on the α-Globin Locus in the Azeri Population of Northwestern Iran. Hemoglobin 40:5, pages 319-322.
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Abbas Khosravi, Mohammadali Jalali-Far, Najmaldin Saki, Hossein Hosseini, Hamid Galehdari, Omid Kiani-Ghalesardi, Mostafa Paridar, Azita Azarkeivan & Kabir Magaji-Hamid. (2016) Evaluation of α-Globin Gene Mutations Among Different Ethnic Groups in Khuzestan Province, Southwest Iran. Hemoglobin 40:2, pages 113-117.
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Samaneh Farashi, Nooshin Bayat, Shadi Vakili, Negin Faramarzi Garous, Mehri Ashki, Hashem Imanian, Hossein Najmabadi & Azita Azarkeivan. (2016) Point mutations which should not be overlooked in Hb H disease. Expert Review of Hematology 9:1, pages 107-113.
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Javad Dehbozorgian, Mohamad Moghadam, Saeed Daryanoush, Sezaneh Haghpanah, Jaber Imani fard, Azam Aramesh, Amin Shahsavani & Mehran Karimi. (2015) Distribution of alpha-thalassemia mutations in Iranian population. Hematology 20:6, pages 359-362.
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Samaneh Farashi, Negin Faramarzi Garous, Fatemeh Zeinali, Shadi Vakili, Mehri Ashki, Hashem Imanian, Hossein Najmabadi, Azita Azarkeivan & Ahmad Tamaddoni. (2015) A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease. Hemoglobin 39:3, pages 196-200.
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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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Arezo Karamzade, Hadi Mirzapour, Majid Hoseinzade, Sara Asadi, Tahere Gholamrezapour, Parvaneh Tavakoli & Mansoor Selebi. (2014) α-Globin Gene Mutations in Isfahan Province, Iran. Hemoglobin 38:3, pages 161-164.
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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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Nasir A.S. Al-Allawi, Sana D. Jalal, Najeeb S. Rasheed, Nooshin Bayat, Hashem Imanian, Hossein Najmabadi & Azad Faraj. (2013) The Spectrum of α-Thalassemia Mutations in the Kurdish Population of Northeastern Iraq. Hemoglobin 37:1, pages 56-64.
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Faramarzi Hossein, Rastegar Mohsen, Moghadami Mohsen & Mohammad Taheri. (2012) α-Thalassemia Mutations in Two Provinces of Southern Iran: FARS & Kohkeloye and Bouyer Ahmad. Hemoglobin 36:2, pages 139-143.
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Haleh Akhavan-Niaki, Ali Banihashemi, Amrollah Mostafazadeh, Vahid Kholghi Oskooei, Mandana Azizi, Reza Youssefi Kamangar & Maryam Mitra Elmi. (2012) Simultaneous Detection of Hb Constant Spring (α142, TAA>CAA, α2) and The α2 IVS-I Donor Site (−TGAGG) Deletion by a Simple Polymerase Chain Reaction-Based Method in Iran. Hemoglobin 36:2, pages 124-130.
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Saedieh Ebrahimkhani, Azita Azarkeivan, Nooshin Bayat, Mahdieh Houry-Parvin, Sayeh Jalil-Nejad, Shima Zand, Zahra Golkar, Valeh Hadavi, Hashem Imanian, Christian Oberkanins & Hossein Najmabadi. (2011) Genotype-Phenotype Correlation In Iranian Patients With Hb H Disease. Hemoglobin 35:1, pages 40-46.
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Nasrollah Saleh-Gohari & Arezo Khosravi-Mashizi. (2010) Spectrum of α-Globin Gene Mutations in the Kerman Province of Iran. Hemoglobin 34:5, pages 451-460.
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Articles from other publishers (5)
Mona Asghari Ahmadabad, Noushin Pourreza, Setareh Ramezanpour, Adel Baghersalimi, Mersedeh Enshaei, Marjan Askari, Amirhossein Alizadeh, Elahe Izadi & Bahram Darbandi. (2023) An analysis of the distribution and spectrum of alpha thalassemia mutations in Rasht City, North of Iran. Frontiers in Pediatrics 11.
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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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Paloma Ropero, Ana Villegas, Jorge M. Nieto, Fernando A. González & Rafael Martínez. (2019) Novel nonsense mutation in the α1-globin gene [HBA1:C.49A>T] is responsible for non-deletion α-thalassemia. Clinical Biochemistry 63, pages 139-142.
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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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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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