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Volume 35, 2011 - Issue 4

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Original Article

Clinicopathological and Radiological Study of Egyptian β-Thalassemia Intermedia and β-Thalassemia Major Patients: Relation to Complications and Response to Therapy

Galila M. MokhtarDepartment of Pediatric, Faculty of Medicine, Ain Shams University, Cairo, Egypt

Azza A.G. TantawyDepartment of Pediatric, Faculty of Medicine, Ain Shams University, Cairo, Egypt

Amira A.M. AdlyDepartment of Pediatric, Faculty of Medicine, Ain Shams University, Cairo, Egypt

Eman A.R. IsmailDepartment of Clinical Pathology, Faculty of Medicine, Ain Shams University, Cairo, EgyptCorrespondence[email protected]

Pages 382-405 | Received 02 Mar 2011, Accepted 05 Mar 2011, Published online: 28 Jul 2011

Cite this article
https://doi.org/10.3109/03630269.2011.598985

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Amal El-Beshlawy, Hany Dewedar, Salwa Hindawi, Salam Alkindi, Azza A. Tantawy, Mohamed A. Yassin & Ali T. Taher. (2023) Management of transfusion-dependent β-thalassemia (TDT): Expert insights and practical overview from the Middle East. Blood Reviews, pages 101138.
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Amit Bhardwaj, Kye Mon Min Swe & Nirmal K Sinha. (2023) Treatment for osteoporosis in people with beta-thalassaemia. Cochrane Database of Systematic Reviews 2023:5.
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Nipith Charoenngam, Thanitsara Rittiphairoj & Ben Ponvilawan. (2021) Fracture prevalence in thalassemia: a systematic review and meta-analysis. Archives of Osteoporosis 16:1.
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Andrea Murtas, Caterina Zanza, Nadia Vacca, Laura Saderi, Giovanni Sotgiu, Claudio Fozza & Roberto Antonucci. (2021) Assessment of Bone Metabolism Alterations in Transfusion-dependent Beta-thalassemia Major: An Observational Study. Journal of Pediatric Hematology/Oncology 43:3, pages 118-119.
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Amira A. Adly & Eman A. Ismail. (2018) Management of Children With β-Thalassemia Intermedia: Overview, Recent Advances, and Treatment Challenges. Journal of Pediatric Hematology/Oncology 40:4, pages 253-268.
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Azza Abdel Gawad Tantawy, Amira Abdel Moneam Adly, Eman Abdel Rahman Ismail, Omneya Ibrahim Youssef & Mohamed ElSayed Ali. (2017) Soluble fms-Like Tyrosine Kinase 1 as a Link Between Angiogenesis and Endothelial Dysfunction in Pediatric Patients With β-Thalassemia Intermedia. Clinical and Applied Thrombosis/Hemostasis 23:8, pages 943-950.
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Riaz Gul, Jasim Dil Wazir & Shandana Rehman. (2017) Different Types of Complications in Patients Suffering from B-Thalassemia (Thalassemia Major). Journal of Gandhara Medical and Dental Science 4:1, pages 28-40.
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Ali H. Algiraigri, Nicola A.M. Wright, Elizabeth Oddone Paolucci & Aliya Kassam. (2017) Hydroxyurea for nontransfusion-dependent β-thalassemia: A systematic review and meta-analysis. Hematology/Oncology and Stem Cell Therapy 10:3, pages 116-125.
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. 2016. The Heart of Africa. The Heart of Africa 245 253 .

Amit Bhardwaj, Kye Mon Min Swe, Nirmal K Sinha & Ifeyinwa Osunkwo. (2016) Treatment for osteoporosis in people with ß-thalassaemia. Cochrane Database of Systematic Reviews.
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Andrea Giusti, Valeria Pinto, Gian Luca Forni & Alberto Pilotto. (2016) Management of beta-thalassemia-associated osteoporosis. Annals of the New York Academy of Sciences 1368:1, pages 73-81.
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Azza Abdel Gawad Tantawy, Amira Abdel Moneam Adly, Eman Abdel Rahman Ismail, Omneya Ibrahim Youssef & Mohamed ElSayed Ali. (2015) Growth differentiation factor-15 in children and adolescents with thalassemia intermedia: Relation to subclinical atherosclerosis and pulmonary vasculopathy. Blood Cells, Molecules, and Diseases 55:2, pages 144-150.
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Abbas Najjari, Mohsen Asouri, Ladan Hosseini Gouhari, Haleh Akhavan Niaki, Amir Sasan Mozaffari Nejad, Seyyedeh Masoumeh Eslami, Hassan Abolghasemi, Ramin Ataee, Abdol Ali Ebrahimi, Masoumeh Rezaei Moshaei & Ali Asghar Ahmadi. (2014) α:Non–α and Gγ:Aγ globin chain ratios in thalassemia intermedia patients treated with hydroxyurea. Asian Pacific Journal of Tropical Biomedicine 4, pages S177-S185.
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Mohsen S. Elalfy, Amira A. M. Adly, Eman A. Ismail, Yasmine I. Elhenawy & Islam R. Elghamry. (2013) Therapeutic superiority and safety of combined hydroxyurea with recombinant human erythropoietin over hydroxyurea in young β-thalassemia intermedia patients. European Journal of Haematology 91:6, pages 522-533.
Crossref

Amit Bhardwaj, Kye Mon Min Swe, Nirmal Kumar Sinha & Ifeyinwa Osunkwo. 1996. Cochrane Database of Systematic Reviews. Cochrane Database of Systematic Reviews.

Azza AG Tantawy, Nevine G. Andrawes, Amany Ismaeil, Solaf A. Kamel & Wessam Emam. (2012) Prevalence of Xmnl Gγ polymorphism in Egyptian patients with β-thalassemia major. Annals of Saudi Medicine 32:5, pages 487-491.
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Clinicopathological and Radiological Study of Egyptian β-Thalassemia Intermedia and β-Thalassemia Major Patients: Relation to Complications and Response to Therapy

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Clinicopathological and Radiological Study of Egyptian β-Thalassemia Intermedia and β-Thalassemia Major Patients: Relation to Complications and Response to Therapy

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