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British Journal of Haematology|June 22, 2010
Outcome of children with sickle cell disease admitted to intensive care - a single institution experienceJack L Bartram, Swee L Thein, Kate Gardner, et al.Plos One|September 26, 2015
Tissue Iron Distribution Assessed by MRI in Patients with Iron Loading AnemiasLucía Gutiérrez, Michael J House, Nisha Vasavda, et al.British Journal of Haematology|March 28, 2013
A randomized phase I/II trial of HQK-1001, an oral fetal globin gene inducer, in β-thalassaemia intermedia and HbE/β-thalassaemiaSuthat Fucharoen, Adlette Inati, Noppadol Siritanaratku, et al.British Journal of Haematology|May 18, 2006
Alpha-haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of beta-thalassaemiaMei I Lai, Jie Jiang, Nicholas Silver, et al.British Journal of Haematology|March 8, 2007
The associations between air quality and the number of hospital admissions for acute pain and sickle-cell disease in an urban environmentDeborah Yallop, Edward R Duncan, Elizabeth Norris, et al.Bioconjugate Chemistry|February 23, 2019
Interactions of an Anti-Sickling Drug with Hemoglobin in Red Blood Cells from a Patient with Sickle Cell AnemiaMichael Brad Strader, Hongying Liang, Fantao Meng, et al.Journal of Medical Screening|August 8, 2022
Newborn screening for abnormal haemoglobins in Jamaica: Practical issues in an island programmeGraham R Serjeant, Beryl E Serjeant, Karlene P Mason, et al.Pageof 2