I. Hambleton

Latest

• Foot ulceration and its association with mortality in diabetes mellitus: a meta-analysis.
• The spectrum of neuropsychiatric lupus in a Black Caribbean population: a report of the Barbados National Lupus Registry.
• A checklist that enhances the provision of education during insulin initiation simulation: a randomized controlled trial.
• Newborn Screening for Sickle Cell Disease: Jamaican Experience.
• Priapism in Homozygous Sickle Cell Disease: A 40-year Study of the Natural History.
• Iron Deficiency among Jamaican Adolescents.
• Global estimates of diabetes prevalence for 2013 and projections for 2035.
• Homozygous sickle cell disease in Uganda and Jamaica a comparison of Bantu and Benin haplotypes.
• Pattern of pregnancy weight gain in homozygous sickle cell disease and effect on birth size.
• Bacterial vaginosis in female facility workers in north-western Tanzania: prevalence and risk factors.
• Predicted declines in sickle allele frequency in Jamaica using empirical data.
• The frequency of the sickle allele in Jamaica has not declined over the last 22 years.
• CDC-defined diseases and opportunistic infections in Jamaican children with HIV/AIDS.
• Socio-demographic characteristics of HIV-exposed and HIV-infected Jamaican children.
• Tuberculosis and HIV co-infections in Jamaican children.
• Uptake of interventions, outcomes and challenges in caring for HIV-exposed infants in Kingston, Jamaica.
• Newborn screening for sickle cell disease in Brazil: the Campinas experience.
• Paediatric HIV/AIDS in Jamaica. A hospital-based description.
• Red cell antibodies in patients with homozygous sickle cell disease: a comparison of patients in Jamaica and the United Kingdom.
• Psychological distress and coping in sickle cell disease: comparison of British and Jamaican attitudes.
• Day-care management of sickle cell painful crisis in Jamaica: a model applicable elsewhere?
• Comparison of responses evoked by mild indirect cooling and by sound in the forearm vasculature in patients with homozygous sickle cell disease and in normal subjects.
• Peripheral vascular response to mild indirect cooling in patients with homozygous sickle cell (SS) disease and the frequency of painful crisis.