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Hemoglobin
international journal for hemoglobin research
Volume 33, 2009 - Issue sup1
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PROCEEDINGS OF THE 1ST PAN-MIDDLE EASTERN CONFERENCE ON HAEMOGLOBINOPATHIES DAMASCUS (SYRIA), 1–2 MAY, 2009 GUEST EDITORS: MICHAEL ANGASTINIOTIS AND ANDROULLA ELEFTHERIOUThe Sixth Section: Thalassemia Intermedia

Hydroxyurea in the Management of Thalassemia Intermedia

Pages S177-S182 | Published online: 13 Dec 2009

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Karim Bayanzay & Ramsha Khan. (2015) Meta-analysis on effectiveness of hydroxyurea to treat transfusion-dependent beta-thalassemia. Hematology 20:8, pages 469-476.
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Mehrnoush Kosaryan, Mandana Zafari, Abbass Alipur & Akbar Hedayatizadeh-Omran. (2014) The Effect and Side Effect of Hydroxyurea Therapy on Patients With β-Thalassemia: A Systematic Review to December 2012. Hemoglobin 38:4, pages 262-271.
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Articles from other publishers (13)

Sirikwan Siriworadetkun, Chayada Thiengtavor, Rattanawan Thubthed, Kittiphong Paiboonsukwong, Suthat Fucharoen, Kovit Pattanapanyasat, Jim Vadolas, Saovaros Svasti & Pornthip Chaichompoo. (2022) A comprehensive study of immune function and immunophenotyping of white blood cells from β‐thalassaemia/ HbE patients on hydroxyurea supports the safety of the drug . British Journal of Haematology 200:3, pages 367-376.
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VR NaghulJerrine JosephMary Shamya ArokiarajanV. Ramesh Kumar. (2022) An invitro evaluation of the cytotoxicity and p53-mediated apoptotic effect of ocimum sanctum leaves hexane extract on human oral cancer cell lines. Asia-Pacific Journal of Oncology, pages 1-9.
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Alexandros Makis, Ersi Voskaridou, Ioannis Papassotiriou & Eleftheria Hatzimichael. (2021) Novel Therapeutic Advances in β-Thalassemia. Biology 10:6, pages 546.
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Sujana Biswas, Arijit Nag, Kanjaksha Ghosh, Rudra Ray, Kaushik Roy, Anish Bandyopadhyay & Maitreyee Bhattacharyya. (2018) Genetic determinants related to pharmacological induction of foetal haemoglobin in transfusion-dependent HbE-β thalassaemia. Annals of Hematology 98:2, pages 289-299.
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Sujana Biswas, Rudra Ray, Kaushik Roy, Anish Bandyopadhyay, Kanjaksha Ghosh & Maitreyee Bhattacharyya. (2019) Alpha Globin Gene Mutation: A Major Determinant of Hydroxyurea Response in Transfusion-Dependent HbE-β-Thalassaemia. Acta Haematologica 142:3, pages 132-141.
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Mehran Karimi, Tahereh Zarei, Sezaneh Haghpanah, Mohamad Moghadam, Ahmad Ebrahimi, Narges Rezaei, Ghazaleh Heidari, Afsaneh Vazin, Maryam Khavari & Hamid R. Miri. (2017) Relationship Between Some Single-nucleotide Polymorphism and Response to Hydroxyurea Therapy in Iranian Patients With β-Thalassemia Intermedia. Journal of Pediatric Hematology/Oncology 39:4, pages e171-e176.
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Amin Abolhasani Foroughi, Hosein Ghaffari, Sezaneh Haghpanah, Masoume Nazeri, Roghieh Ghaffari, Marzieh Bardestani & Mehran Karimi. (2015) Comparative Study of Radiographic and Laboratory Findings Between Beta Thalassemia Major and Beta Thalassemia Intermedia Patients With and Without Treatment by Hydroxyurea. Iranian Red Crescent Medical Journal 17:2.
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Sushmita Nair, Lamis K Eldjerou, Neil S. Harris & Levette N. Dunbar. (2014) Rare form of autosomal dominant thalassemia-Hemoglobin Hakkari. Pediatric Blood & Cancer 61:11, pages 2118-2120.
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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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Mohammad Reza Bordbar, Samir Silavizadeh, Sezaneh Haghpanah, Roza Kamfiroozi, Marzieh Bardestani & Mehran Karimi. (2014) Hydroxyurea Treatment in Transfusion-Dependent ?-Thalassemia Patients. Iranian Red Crescent Medical Journal 16:6.
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John Old. 2014. Reference Module in Biomedical Sciences. Reference Module in Biomedical Sciences.
Mehran Karimi, Sezaneh Haghpanah, Ali Farhadi & Majid Yavarian. (2011) Genotype–phenotype relationship of patients with β-thalassemia taking hydroxyurea: a 13-year experience in Iran. International Journal of Hematology 95:1, pages 51-56.
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Yelena Ginzburg & Stefano Rivella. (2011) β-thalassemia: a model for elucidating the dynamic regulation of ineffective erythropoiesis and iron metabolism. Blood 118:16, pages 4321-4330.
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