Citations (15)
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Hassan Abolghasemi, Sharareh Kamfar, Azita Azarkeivan, Mehran Karimi, Bijan Keikhaei, Fahimeh Abolghasemi, Mohammad H. Radfar, Peyman Eshghi & Samin Alavi. (2022) Clinical and genetic characteristics of hemoglobin H disease in Iran. Pediatric Hematology and Oncology 39:6, pages 489-499.
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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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Xi Yao, Lu-Hong Xu, Hong-Gui Xu, Xin-Yu Li, Yong Liu & Jian-Pei Fang. (2019) Iron Metabolism and Oxidative Status in Patients with Hb H Disease. Hemoglobin 43:1, pages 38-41.
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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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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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Samaneh Farashi, Negin Faramarzi Garous, Mehri Ashki, Shadi Vakili, Fatemah Zeinali, Hashem Imanian, Azita Azarkeivan & Hossein Najmabadi. (2015) Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient. Hemoglobin 39:3, pages 152-155.
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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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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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Articles from other publishers (7)
Duantida Songdej, Manunya Tandhansakul, Pakawan Wongwerawattanakoon, Nongnuch Sirachainan, Pimlak Charoenkwan & Ampaiwan Chuansumrit. (2023) Severity scoring system to guide transfusion management in pediatric non‐deletional HbH. Pediatrics International 65:1.
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Mohammad Hamid, Bijan keikhaei, Hamid Galehdari, Alihossein Saberi, Alireza Sedaghat, Gholamreza Shariati & Marziye Mohammadi-Anaei. (2022) Genotype–phenotype correlation in patients with deletional and nondeletional mutations of Hb H disease in Southwest of Iran. Scientific Reports 12:1.
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Rawand P. Shamoon, Ahmed K. Yassin, Ranan K. Polus & Mohamad D. Ali. (2020) Genotype-phenotype correlation of HbH disease in northern Iraq. BMC Medical Genetics 21:1.
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Mostafa Paridar, Ebrahim Azizi, Bijan Keikhaei, Vahideh Takhviji, Iman Baluchi & Abbas Khosravi. (2019) Iranian patients with hemoglobin H disease: genotype–phenotype correlation. Molecular Biology Reports 46:5, pages 5041-5048.
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Samaneh Farashi & Hossein Najmabadi. (2015) Diagnostic pitfalls of less well recognized HbH disease. Blood Cells, Molecules, and Diseases 55:4, pages 387-395.
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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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. (2011) Heterogeneity of Hemoglobin H Disease in Childhood. New England Journal of Medicine 364:21, pages 2069-2072.
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