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Hydroxyurea for Primary Stroke Prevention: The time draweth nigh

Pediatric blood & cancer, 2019-03, Vol.66 (3), p.e27536-n/a

Reid, Marvin E

2019

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Determining glomerular filtration rate in homozygous sickle cell disease: utility of serum creatinine based estimating equations

PloS one, 2013-07, Vol.8 (7), p.e69922-e69922

2013

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Edematous severe acute malnutrition is characterized by hypomethylation of DNA

Nature communications, 2019-12, Vol.10 (1), p.5791-13, Article 5791

2019

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Impact of a Comprehensive Sickle Cell Center on Early Childhood Mortality in a Developing Country: The Jamaican Experience

The Journal of pediatrics, 2015-09, Vol.167 (3), p.702-705.e1

2015

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Academic performance in Jamaican children with sickle cell disease

Journal of the National Medical Association, 2023-10, Vol.115 (5), p.475-481

2023

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Excess risk of maternal death from sickle cell disease in Jamaica: 1998-2007

PloS one, 2011-10, Vol.6 (10), p.e26281-e26281

2011

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Variant-aware saturating mutagenesis using multiple Cas9 nucleases identifies regulatory elements at trait-associated loci

Nature genetics, 2017-04, Vol.49 (4), p.625-634

2017

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Use of a public park for physical activity in the Caribbean: evidence from a mixed methods study in Jamaica

BMC public health, 2019-07, Vol.19 (1), p.894-894, Article 894

2019

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An Investigation of the Antioxidant Capacity in Extracts from Moringa oleifera Plants Grown in Jamaica

Plants (Basel), 2017-10, Vol.6 (4), p.48

2017

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Blood viscosity and the expression of inflammatory and adhesion markers in homozygous sickle cell disease subjects with chronic leg ulcers

PloS one, 2013-07, Vol.8 (7), p.e68929-e68929

2013

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Utility of WHOQOL-BREF in measuring quality of life in sickle cell disease

Health and quality of life outcomes, 2009-08, Vol.7 (1), p.75-75, Article 75

2009

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Higher rates of hemolysis are not associated with albuminuria in Jamaicans with sickle cell disease

PloS one, 2011-04, Vol.6 (4), p.e18863-e18863

2011

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The incidence of VP shunt infection in a middle-income nation: a retrospective analysis of a pediatric population

Frontiers in surgery, 2023-12, Vol.10, p.1304105-1304105

2023

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Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation

Haematologica (Roma), 2011-11, Vol.96 (11), p.1589-1594

2011

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Depression and loneliness in Jamaicans with sickle cell disease

BMC psychiatry, 2010-06, Vol.10 (1), p.40-40, Article 40

2010

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Prevention of conversion to abnormal transcranial Doppler with hydroxyurea in sickle cell anemia: A Phase III international randomized clinical trial

American journal of hematology, 2015-12, Vol.90 (12), p.1099-1105

2015

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A double‐blind, placebo‐controlled phase II study of the efficacy and safety of 2,2‐dimethylbutyrate (HQK‐1001), an oral fetal globin inducer, in sickle cell disease

American journal of hematology, 2014-07, Vol.89 (7), p.709-713

2014

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Plasma concentration of platelet-derived microparticles is related to painful vaso-occlusive phenotype severity in sickle cell anemia

PloS one, 2014-01, Vol.9 (1), p.e87243-e87243

2014

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Renal function in adult Jamaicans with homozygous sickle cell disease

Hematology (Luxembourg), 2015-08, Vol.20 (7), p.422-428

2015

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Prevalence and distribution of ampc beta-lactamase producing escherichia coli and klebsiella pneumoniae isolates obtained from urine samples at a tertiary care hospital in the caribbean

Frontiers in cellular and infection microbiology, 2022-10, Vol.12, p.1015633-1015633

2022

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A trial comparing the use of rectal misoprostol plus perivascular vasopressin with perivascular vasopressin alone to decrease myometrial bleeding at the time of abdominal myomectomy

Fertility and sterility, 2013-10, Vol.100 (4), p.1044-1049

2013

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Overactive bladder in adults with sickle cell disease

Neurourology and urodynamics, 2016-06, Vol.35 (5), p.642-646

2016

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Knowledge and health beliefs of Jamaican adolescents with sickle cell disease

Pediatric blood & cancer, 2011-12, Vol.57 (6), p.1044-1048

2011

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A dose‐escalation phase IIa study of 2,2‐dimethylbutyrate (HQK‐1001), an oral fetal globin inducer, in sickle cell disease

American journal of hematology, 2013-11, Vol.88 (11), p.E255-E260

2013

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University consortium to address public health priorities and research capacity building in the Caribbean

Frontiers in education (Lausanne), 2023-11, Vol.8

2023

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Hydroxyurea for Primary Stroke Prevention: The time draweth nigh

Determining glomerular filtration rate in homozygous sickle cell disease: utility of serum creatinine based estimating equations

Edematous severe acute malnutrition is characterized by hypomethylation of DNA

Impact of a Comprehensive Sickle Cell Center on Early Childhood Mortality in a Developing Country: The Jamaican Experience

Academic performance in Jamaican children with sickle cell disease

Excess risk of maternal death from sickle cell disease in Jamaica: 1998-2007

Variant-aware saturating mutagenesis using multiple Cas9 nucleases identifies regulatory elements at trait-associated loci

Use of a public park for physical activity in the Caribbean: evidence from a mixed methods study in Jamaica

An Investigation of the Antioxidant Capacity in Extracts from Moringa oleifera Plants Grown in Jamaica

Blood viscosity and the expression of inflammatory and adhesion markers in homozygous sickle cell disease subjects with chronic leg ulcers

Utility of WHOQOL-BREF in measuring quality of life in sickle cell disease

Higher rates of hemolysis are not associated with albuminuria in Jamaicans with sickle cell disease

The incidence of VP shunt infection in a middle-income nation: a retrospective analysis of a pediatric population

Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation

Depression and loneliness in Jamaicans with sickle cell disease

Prevention of conversion to abnormal transcranial Doppler with hydroxyurea in sickle cell anemia: A Phase III international randomized clinical trial

A double‐blind, placebo‐controlled phase II study of the efficacy and safety of 2,2‐dimethylbutyrate (HQK‐1001), an oral fetal globin inducer, in sickle cell disease

Plasma concentration of platelet-derived microparticles is related to painful vaso-occlusive phenotype severity in sickle cell anemia

Renal function in adult Jamaicans with homozygous sickle cell disease

Prevalence and distribution of ampc beta-lactamase producing escherichia coli and klebsiella pneumoniae isolates obtained from urine samples at a tertiary care hospital in the caribbean

A trial comparing the use of rectal misoprostol plus perivascular vasopressin with perivascular vasopressin alone to decrease myometrial bleeding at the time of abdominal myomectomy

Overactive bladder in adults with sickle cell disease

Knowledge and health beliefs of Jamaican adolescents with sickle cell disease

A dose‐escalation phase IIa study of 2,2‐dimethylbutyrate (HQK‐1001), an oral fetal globin inducer, in sickle cell disease

University consortium to address public health priorities and research capacity building in the Caribbean

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