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Complications of thalassemia major and their treatment

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Pages 353-366 | Published online: 10 Jan 2014

Keep up to date with the latest research on this topic with citation updates for this article.

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Ibrahim M Gosadi, Gassem A Gohal, Alanoud E Dalak, Anas A Alnami, Norah A Aljabri & Atyaf J Zurayyir. (2021) Assessment of Factors Associated with the Effectiveness of Premarital Screening for Hemoglobinopathies in the South of Saudi Arabia. International Journal of General Medicine 14, pages 3079-3086.
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Koorosh Etemad, Parisa Mohseni, Mohammad Aghighi, Ayad Bahadorimonfared, Razieh Hantooshzadeh, Niloufar Taherpour, Negar Piri, Sahar Sotoodeh Ghorbani, Fatemeh Malek, Fatemeh Kheiry, Azimeh Khodami, Tannaz Valadbeigi & Mahmoud Hajipour. (2021) Quality of Life and Related Factors in β-Thalassemia Patients. Hemoglobin 45:4, pages 245-249.
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Mohamed A. Eid & Sobhy M. Aly. (2021) Effect of whole body vibration training on bone mineral density and functional capacity in children with thalassemia. Physiotherapy Theory and Practice 37:2, pages 279-286.
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Vigneshwaran Venkatesan, Saranya Srinivasan, Prathibha Babu & Saravanabhavan Thangavel. (2021) Manipulation of Developmental Gamma-Globin Gene Expression: an Approach for Healing Hemoglobinopathies. Molecular and Cellular Biology 41:1.
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Maria Marsella & Paolo Ricchi. (2019) Thalassemia and hepatocellular carcinoma: links and risks. Journal of Blood Medicine 10, pages 323-334.
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M. Yousuf Yassouf, Faizeh Alquobaili, Younes Kabalan & Yasser Mukhalalaty. (2019) Compliance with Deferoxamine Therapy and Thyroid Dysfunction of Patients with β-Thalassemia Major in Syria. Hemoglobin 43:3, pages 218-221.
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Alessia Finotti, Monica Borgatti, Nicoletta Bianchi, Cristina Zuccato, Ilaria Lampronti & Roberto Gambari. (2016) Orphan Drugs and Potential Novel Approaches for Therapies of β-Thalassemia: Current Status and Future Expectations. Expert Opinion on Orphan Drugs 4:3, pages 299-315.
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George Ghartey-Kwansah, Johnson N. Boampong, Benjamin Aboagye, Richmond Afoakwah, Elvis O. Ameyaw & Neils B. Quashie. (2016) The Prevalence of α-Thalassemia and Its Relation to Plasmodium falciparum Infection in Patients Presenting to Clinics in Two Distinct Ecological Zones in Ghana. Hemoglobin 40:1, pages 32-37.
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Nonglak Boonchooduang, Orawan Louthrenoo, Worawut Choeyprasert & Pimlak Charoenkwan. (2015) Health-Related Quality of Life in Adolescents with Thalassemia. Pediatric Hematology and Oncology 32:5, pages 341-348.
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Maria Domenica Cappellini, Vip Viprakasit & Ali T Taher. (2014) An overview of current treatment strategies for β-thalassemia. Expert Opinion on Orphan Drugs 2:7, pages 665-679.
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Laura Breda, Stefano Rivella, Cristina Zuccato & Roberto Gambari. (2013) Combining gene therapy and fetal hemoglobin induction for treatment of β-thalassemia. Expert Review of Hematology 6:3, pages 255-264.
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Roberto Gambari. (2012) Alternative options for DNA-based experimental therapy of β-thalassemia. Expert Opinion on Biological Therapy 12:4, pages 443-462.
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Alessandro Baldan, Andrea Giusti, Cristina Bosi, Cristina Malaventura, Marco Musso, Gian Luca Forni, Stefano Volpato, Giovanni Zuliani & Caterina Borgna-Pignatti. (2015) Klotho, a new marker for osteoporosis and muscle strength in β-thalassemia major. Blood Cells, Molecules, and Diseases 55:4, pages 396-401.
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Yu-Guang Chen, Te-Yu Lin, Cheng-Li Lin, Ming-Shen Dai, Ching-Liang Ho & Chia-Hung Kao. (2015) Risk of Erectile Dysfunction in Transfusion-naive Thalassemia Men. Medicine 94:13, pages e700.
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Dimitrios Kountouras, Nikolaos J. Tsagarakis, Evangelia Fatourou, Efthimios Dalagiorgos, Nikolaos Chrysanthos, Helen Berdoussi, Niki Vgontza, Markissia Karagiorga, Athanasios Lagiandreou, Konstantinos Kaligeros, Ersi Voskaridou, Paraskevi Roussou, Evanthia Diamanti‐Kandarakis & John Koskinas. (2013) Liver disease in adult transfusion‐dependent beta‐thalassaemic patients: investigating the role of iron overload and chronic HCV infection. Liver International 33:3, pages 420-427.
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