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Hematology Volume 22, 2017 - Issue 10
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Thalassemia

Revisiting beta thalassemia intermedia: past, present, and future prospects

Naouel Ben SalahFaculty of Medicine Tunis, University Tunis El Manar, Tunis, TunisiaCorrespondence[email protected]
ORCID Iconhttp://orcid.org/0000-0003-0166-7715
ORCID Icon,
Rayan Bou-FakhredinDepartment of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon
,
Fethi MellouliFaculty of Medicine Tunis, National Center of Bone Marrow Graft, University Tunis El Manar, Tunis, Tunisia
&
Ali T. TaherDepartment of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon
Pages 607-616 | Published online: 07 Jun 2017

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Mohammadreza Saeidnia, Pooria Fazeli, Arghavan Farzi, Maryam Atefy Nezhad, Mojtaba Shabani-Borujeni, Mehran Erfani, Gholamhossein Tamaddon & Mehran Karimi. (2023) An Expert Overview on Therapies in Non-Transfusion-Dependent Thalassemia: Classical to Cutting Edge in Treatment. Hemoglobin 47:2, pages 56-70.
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Articles from other publishers (12)

Amrita Panja, Brahmarshi Das, Tuphan Kanti Dolai & Sujata Maiti Choudhury. 2023. Thalassemia Syndromes - New Insights and Transfusion Modalities. Thalassemia Syndromes - New Insights and Transfusion Modalities.
Antonella Meloni, Michela Parravano, Laura Pistoia, Alberto Cossu, Emanuele Grassedonio, Stefania Renne, Priscilla Fina, Anna Spasiano, Alessandra Salvo, Sergio Bagnato, Calogera Gerardi, Zelia Borsellino, Filippo Cademartiri & Vincenzo Positano. (2023) Phenotypic Clustering of Beta-Thalassemia Intermedia Patients Using Cardiovascular Magnetic Resonance. Journal of Clinical Medicine 12:21, pages 6706.
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Sheetal Mahajan, SACHIN DHULE & TAKSANDE RV. (2023) PREVALENCE AND PROFILE OF BETA-THALASSEMIA: A PROSPECTIVE ANALYSIS AT A TERTIARY CARE CANTER. Asian Journal of Pharmaceutical and Clinical Research, pages 174-176.
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Egarit Noulsri & Surada Lerdwana. (2023) Blood Donors with Thalassemic Trait, Glucose-6-Phosphate Dehydrogenase Deficiency Trait, and Sickle Cell Trait and Their Blood Products: Current Status and Future Perspective. Laboratory Medicine 54:1, pages 6-12.
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Farah Abdulhai, Miran A. Jaffa, Joseph Elias, Patrick Zakka, Mostafa Hotait, Rayan Bou-Fakhredin, Samir Arnaout, Ali T. Taher & Marwan M. Refaat. (2021) Digital thermography and vascular involvement in β-thalassemia intermedia. Annals of Hematology 100:10, pages 2471-2477.
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Hayder Al-Momen, Hussein Khudhair Hussein, Zaid Al-Attar & Mohammed Jalal Hussein. (2020) Green tea influence on iron overload in thalassemia intermedia patients: a randomized controlled trial. F1000Research 9, pages 1136.
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Lourdes del Carmen Rizo de la Torre, Francisco Javier Perea Díaz, Bertha Ibarra Cortés, Víctor Manuel Rentería López, Josefina Yoaly Sánchez López, Francisco Javier Sánchez Anzaldo, María Teresa Magaña Torres, Katia Gonnet, Catherine Badens & Nathalie Bonello-Palot. (2019) Three Mexican Families with β thalassemia intermedia with different molecular basis. Genetics and Molecular Biology 42:4.
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Ariel L. Reinish & Suzie A. Noronha. 2019. Anemia in the Young and Old. Anemia in the Young and Old 95 135 .
Karine Sii-Felice, Marie Giorgi, Philippe Leboulch & Emmanuel Payen. (2018) Hemoglobin disorders: lentiviral gene therapy in the starting blocks to enter clinical practice. Experimental Hematology 64, pages 12-32.
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Rayan Bou-Fakhredin, Joseph Elias & Ali T. Taher. (2018) Iron Overload and Chelation Therapy in Hemoglobinopathies. Thalassemia Reports 8:1, pages 7478.
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Joseph Sleiman, Ali Tarhini, Rayan Bou-Fakhredin, Antoine Saliba, Maria Cappellini & Ali Taher. (2018) Non-Transfusion-Dependent Thalassemia: An Update on Complications and Management. International Journal of Molecular Sciences 19:1, pages 182.
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Hayder Al-MomenShaymaa Kadhim JasimQays Ahmed HassanHayder Hussein Ali. (2018) Relationship between liver iron concentration determined by R2-MRI, serum ferritin, and liver enzymes in patients with thalassemia intermedia. Blood Research 53:4, pages 314.
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