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PRESENTED AT THE INTERNATIONAL CONFERENCE ON HEMOGLOBIN DISORDERS, KUWAIT, February 5–7th, 2011

Limitations of Hb F as a Phenotypic Modifier in Sickle Cell Disease: Study of Kuwaiti Arab Patients

Pages 607-617 | Received 14 Jul 2011, Accepted 26 Jul 2011, Published online: 14 Oct 2011

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Gift D Pule, Shaheen Mowla, Nicolas Novitzky, Charles S Wiysonge & Ambroise Wonkam. (2015) A systematic review of known mechanisms of hydroxyurea-induced fetal hemoglobin for treatment of sickle cell disease. Expert Review of Hematology 8:5, pages 669-679.
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Articles from other publishers (10)

Adekunle Adekile. (2021) The Genetic and Clinical Significance of Fetal Hemoglobin Expression in Sickle Cell Disease. Medical Principles and Practice 30:3, pages 201-211.
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Ambroise Wonkam. (2017) Is there a role for pharmacogenetics in the treatment of sickle cell disease?. Pharmacogenomics 18:4, pages 321-325.
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Gregory J. Kato, Martin H. Steinberg & Mark T. Gladwin. (2017) Intravascular hemolysis and the pathophysiology of sickle cell disease. Journal of Clinical Investigation 127:3, pages 750-760.
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Khuthala MnikaGift D. PuleCollet DandaraAmbroise Wonkam. (2016) An Expert Review of Pharmacogenomics of Sickle Cell Disease Therapeutics: Not Yet Ready for Global Precision Medicine. OMICS: A Journal of Integrative Biology 20:10, pages 565-574.
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Martin H. Steinberg. 2016. Sickle Cell Anemia. Sickle Cell Anemia 49 73 .
Abdulrahman Alsultan, Mohammed K. Alabdulaali, Paula J. Griffin, Ahmed M. AlSuliman, Hazem A. Ghabbour, Paola Sebastiani, Waleed H. Albuali, Amein K. Al-Ali, David H. K. Chui & Martin H. Steinberg. (2014) Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign. British Journal of Haematology 164:4, pages 597-604.
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Martin H. SteinbergDavid H. K. ChuiGeorge J. DoverPaola Sebastiani & Abdulrahman Alsultan. (2014) Fetal hemoglobin in sickle cell anemia: a glass half full?. Blood 123:4, pages 481-485.
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Duyen Ngo, Harold Bae, Martin H. Steinberg, Paola Sebastiani, Nadia Solovieff, Clinton T. Baldwin, Efthymia Melista, Surinder Safaya, Lindsay A. Farrer, Ahmed M. Al-Suliman, Waleed H. Albuali, Muneer H. Al Bagshi, Zaki Naserullah, Idowu Akinsheye, Patrick Gallagher, Hong-yuan Luo, David H.K. Chui, John J. Farrell, Amein K. Al-Ali & Abdulrahman Alsultan. (2013) Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype. Blood Cells, Molecules, and Diseases 51:1, pages 22-26.
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Jo Howard, Moira Malfroy, Charlotte Llewelyn, Louise Choo, Renate Hodge, Tony Johnson, Shilpi Purohit, David C Rees, Louise Tillyer, Isabeau Walker, Karin Fijnvandraat, Melanie Kirby-Allen, Eldon Spackman, Sally C Davies & Lorna M Williamson. (2013) The Transfusion Alternatives Preoperatively in Sickle Cell Disease (TAPS) study: a randomised, controlled, multicentre clinical trial. The Lancet 381:9870, pages 930-938.
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Martin H. Steinberg & Paola Sebastiani. (2012) Genetic modifiers of sickle cell disease. American Journal of Hematology 87:8, pages 795-803.
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