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Articles

Validation of the SF-36 in Jamaicans with sickle-cell disease

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Pages 606-618 | Received 15 Jul 2008, Accepted 01 May 2009, Published online: 19 Oct 2009

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Sharon A. Singh, Nitya Bakshi, Prashant Mahajan & Claudia R. Morris. (2020) What is the future of patient-reported outcomes in sickle-cell disease?. Expert Review of Hematology 13:11, pages 1165-1173.
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Matthew S. Karafin, Arun Singavi, Jawad Hussain, Nancy Wandersee, Thomas Heinrich, Robert W. Hurley, Liyun Zhang, Pippa Simpson & Joshua J. Field. (2018) Predictive factors of daily opioid use and quality of life in adults with sickle cell disease. Hematology 23:10, pages 856-863.
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Roger C. Gibson, Kai A.D. Morgan, Wendel D. Abel, Clayton A. Sewell, Jacqueline S. Martin, Gillian A. Lowe, Winston De La Haye, Christopher L. Edwards, Keisha N. O’Garo, Marvin E. Reid & Monika R. Asnani. (2013) Locus of control, depression and quality of life among persons with sickle cell disease in Jamaica. Psychology, Health & Medicine 18:4, pages 451-460.
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Articles from other publishers (8)

Francesca Rodigari, Giorgia Brugnera & Raffaella Colombatti. (2022) Health-related quality of life in hemoglobinopathies: A systematic review from a global perspective. Frontiers in Pediatrics 10.
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Belinda F. Morrison, Wendy Madden, Monika Asnani, Ayodeji Sotimehin, Uzoma Anele, Yuezhou Jing, Bruce J. Trock & Arthur L. Burnett. (2021) External validation of the priapism impact profile in a Jamaican cohort of patients with sickle cell disease. PLOS ONE 16:10, pages e0258560.
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Adedokun Oluwafemi Ojelabi, Afolabi Elijah Bamgboye & Jonathan Ling. (2019) Preference-based measure of health-related quality of life and its determinants in sickle cell disease in Nigeria. PLOS ONE 14:11, pages e0223043.
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Soheir S. Adam, Charlene M. FlahiffShital Kamble, Marilyn J. TelenShelby D. Reed & Laura M. De Castro. (2017) Depression, quality of life, and medical resource utilization in sickle cell disease. Blood Advances 1:23, pages 1983-1992.
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Marsha J. Treadwell, Kathryn Hassell, Roger Levine & San Keller. (2014) Adult Sickle Cell Quality-of-Life Measurement Information System (ASCQ-Me). The Clinical Journal of Pain 30:10, pages 902-914.
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Julie A. Panepinto. (2012) Health-related quality of life in patients with hemoglobinopathies. Hematology 2012:1, pages 284-289.
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Julie A. Panepinto & Melanie Bonner. (2012) Health-related quality of life in sickle cell disease: Past, present, and future. Pediatric Blood & Cancer 59:2, pages 377-385.
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Monika R Asnani, Garth E Lipps & Marvin E Reid. (2009) Utility of WHOQOL-BREF in measuring quality of life in Sickle Cell Disease. Health and Quality of Life Outcomes 7:1.
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