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British Journal of Haematology|December 11, 2012
Increased leucocyte apoptosis in transfused β-thalassaemia patientsPatrick B Walter, John Porter, Patricia Evans, et al.
Blood|July 21, 2011
Risk factors and mortality associated with an elevated tricuspid regurgitant jet velocity measured by Doppler-echocardiography in thalassemia: a Thalassemia Clinical Research Network reportClaudia R Morris, Hae-Young Kim, Felicia Trachtenberg, et al.
Transfusion|February 6, 2019
Identification of red blood cell antibodies in maternal breast milk implicated in prolonged hemolytic disease of the fetus and newbornAlexis Leonard, Lauren Hittson Boal, Philippe Pary, et al.
British Journal of Haematology|November 5, 2013
Validation and reliability of a disease-specific quality of life measure (the TranQol) in adults and children with thalassaemia majorRobert J Klaassen, Nicholas Barrowman, Manuela Merelles-Pulcini, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|May 7, 2011
Intestinal SR-BI is upregulated in insulin-resistant states and is associated with overproduction of intestinal apoB48-containing lipoproteinsAmanda A Hayashi, Jennifer Webb, Joanna Choi, et al.
Studies in Health Technology and Informatics|May 31, 2014
Virtual reality graded exposure therapy with arousal control for the treatment of combat related posttraumatic stress disorder: a follow up case seriesDennis Patrick Wood, Robert L Mclay, Jennifer Webb-Murphy, et al.
Transfusion|November 24, 2024
Adding hydroxyurea to chronic transfusion therapy for sickle cell anemia reduces transfusion burdenRobert Sheppard Nickel, Stefanie Margulies, Karuna Panchapakesan, et al.
Blood Advances|January 28, 2020
American Society of Hematology 2020 guidelines for sickle cell disease: transfusion supportStella T Chou, Mouaz Alsawas, Ross M Fasano, et al.
Blood|January 27, 2012
Chelation use and iron burden in North American and British thalassemia patients: a report from the Thalassemia Longitudinal CohortJanet L Kwiatkowski, Hae-Young Kim, Alexis A Thompson, et al.
British Journal of Haematology|July 17, 2009
Differences in the prevalence of growth, endocrine and vitamin D abnormalities among the various thalassaemia syndromes in North AmericaMaria G Vogiatzi, Eric A Macklin, Felicia L Trachtenberg, et al.
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