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Hemoglobin
international journal for hemoglobin research
Volume 25, 2001 - Issue 1
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CLINICAL AND HEMATOLOGICAL RESPONSES TO HYDROXYUREA IN SICILIAN PATIENTS WITH Hb S/β-THALASSEMIA

Paolo Rigano “V. Cervello” Hospital, Thalassaemia Centre, Research Unit “P. Cutino”, Palermo, 90147, ItalyCorrespondence[email protected]
,
Griffin P. Rodgers National Institute of Health, Molecular and Clinical Hematology Branch, Bethesda, MD, 20892-0001, U.S.A.
,
Disma Renda “V. Cervello” Hospital, Thalassaemia Centre, Research Unit “P. Cutino”, Palermo, 90147, Italy
,
Maria C. Renda “V. Cervello” Hospital, Thalassaemia Centre, Research Unit “P. Cutino”, Palermo, 90147, Italy
,
Alessandra Aquino “V. Cervello” Hospital, Thalassaemia Centre, Research Unit “P. Cutino”, Palermo, 90147, Italy
&
Aurelio Maggio “V. Cervello” Hospital, Thalassaemia Centre, Research Unit “P. Cutino”, Palermo, 90147, Italy
Pages 9-17 | Received 19 Jul 2000, Accepted 19 Oct 2000, Published online: 07 Jul 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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Alessia Finotti & Roberto Gambari. (2014) Recent trends for novel options in experimental biological therapy of β-thalassemia. Expert Opinion on Biological Therapy 14:10, pages 1443-1454.
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Articles from other publishers (12)

Paolo Rigano, Lucia De Franceschi, Laura Sainati, Antonio Piga, Frédéric B. Piel, Maria Domenica Cappellini, Carmelo Fidone, Nicoletta Masera, Giovanni Palazzi, Barbara Gianesin & Gian Luca Forni. (2018) Real-life experience with hydroxyurea in sickle cell disease: A multicenter study in a cohort of patients with heterogeneous descent. Blood Cells, Molecules, and Diseases 69, pages 82-89.
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Maria Stella Figueiredo. (2015) The compound state: Hb S/beta-thalassemia. Revista Brasileira de Hematologia e Hemoterapia 37:3, pages 150-152.
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Alice Pecoraro, Paolo Rigano, Antonio Troia, Roberta Calzolari, Concetta Scazzone, Aurelio Maggio, Martin H. Steinberg & Rosalba Di Marzo. (2014) Quantification of HBG mRNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta-thalassemia . European Journal of Haematology 92:1, pages 66-72.
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Paolo Rigano, Alice Pecoraro, Giuseppina Calvaruso, Martin H. Steinberg, Sonia Iannello & Aurelio Maggio. (2013) Cerebrovascular events in sickle cell‐beta thalassemia treated with hydroxyurea: A single center prospective survey in adult Italians. American Journal of Hematology 88:11.
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Sujit Sheth, Maureen Licursi & Monica Bhatia. (2013) Sickle cell disease: time for a closer look at treatment options?. British Journal of Haematology 162:4, pages 455-464.
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Khaled M. MusallamAli T. TaherMaria Domenica CappelliniVijay G. Sankaran. (2013) Clinical experience with fetal hemoglobin induction therapy in patients with β-thalassemia. Blood 121:12, pages 2199-2212.
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John Old. 2013. Emery and Rimoin's Principles and Practice of Medical Genetics. Emery and Rimoin's Principles and Practice of Medical Genetics 1 44 .
M. de Montalembert. (2008) Traitement des patients drépanocytaires par hydroxyurée : efficacité et tolérance. Transfusion Clinique et Biologique 15:1-2, pages 34-38.
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F. Mellouli & M. Bejaoui. (2008) L’utilisation de l’hydroxyurée dans les formes sévères de la drépanocytose : étude de 47 cas pédiatriques tunisiens. Archives de Pédiatrie 15:1, pages 24-28.
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Sally C Davies & Annette Gilmore. (2003) The role of hydroxyurea in the management of sickle cell disease. Blood Reviews 17:2, pages 99-109.
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Christina Halsey & Irene A. G. Roberts. (2003) The role of hydroxyurea in sickle cell disease. British Journal of Haematology 120:2, pages 177-186.
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M.C. McGuinness, H.-P. Zhang & K.D. Smith. (2001) Evaluation of Pharmacological Induction of Fatty Acid β-Oxidation in X-Linked Adrenoleukodystrophy. Molecular Genetics and Metabolism 74:1-2, pages 256-263.
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