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Recent Advances in the Treatment of Sickle Cell Disease

Frontiers in physiology, 2020-05, Vol.11, p.435-435

2020

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Tissue Iron Distribution Assessed by MRI in Patients with Iron Loading Anemias

PloS one, 2015-09, Vol.10 (9), p.e0139220-e0139220

2015

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Delayed haemolytic transfusion reaction in adults with sickle cell disease: a 5‐year experience

British journal of haematology, 2015-06, Vol.169 (5), p.746-753

2015

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How we treat delayed haemolytic transfusion reactions in patients with sickle cell disease

British journal of haematology, 2015-09, Vol.170 (6), p.745-756

2015

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Sickle cell nephropathy – a practical approach

British journal of haematology, 2011-11, Vol.155 (3), p.287-297

2011

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World Sickle Cell Day 2016 : A time for appraisal

Indian journal of medical research (New Delhi, India : 1994), 2016-06, Vol.143 (6), p.678

2016

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Interim assessment of liver damage in patients with sickle cell disease using new non‐invasive techniques

British journal of haematology, 2017-02, Vol.176 (4), p.643-650

2017

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Interactions of an Anti-Sickling Drug with Hemoglobin in Red Blood Cells from a Patient with Sickle Cell Anemia

Bioconjugate chemistry, 2019-03, Vol.30 (3), p.568-571

2019

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A randomized phase I/II trial of HQK‐1001, an oral fetal globin gene inducer, in β‐thalassaemia intermedia and HbE/β‐thalassaemia

British journal of haematology, 2013-05, Vol.161 (4), p.587-593

2013

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Newborn screening for abnormal haemoglobins in Jamaica: Practical issues in an island programme

Journal of medical screening, 2022-12, Vol.29 (4), p.219-223

2022

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Haemoglobin Variant Screening in Jamaica: Meeting Student's Request

British journal of haematology, 2016-02, Vol.172 (4), p.634-636

2016

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A Twins Heritability Study on Alpha Hemoglobin Stabilizing Protein (AHSP) Expression Variability

Twin research and human genetics, 2010-12, Vol.13 (6), p.567-572

2010

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Effects of co-existing α-thalassaemia in sickle cell disease on hydroxycarbamide therapy and circulating nucleic acids

British journal of haematology, 2012-04, Vol.157 (2), p.249-252

2012

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Renal iron load in sickle cell disease is influenced by severity of haemolysis

British journal of haematology, 2012-06, Vol.157 (5), p.599-605

2012

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Outcome of adults with sickle cell disease admitted to critical care – experience of a single institution in the UK

British journal of haematology, 2010-09, Vol.150 (5), p.610-613

2010

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α‐Haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of β‐thalassaemia

British journal of haematology, 2006-06, Vol.133 (6), p.675-682

2006

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Outcome of children with sickle cell disease admitted to intensive care – a single institution experience

British journal of haematology, 2010-09, Vol.150 (5), p.614-617

2010

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The associations between air quality and the number of hospital admissions for acute pain and sickle‐cell disease in an urban environment

British journal of haematology, 2007-03, Vol.136 (6), p.844-848

2007

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A randomized phase I/II trial of HQK ‐1001, an oral fetal globin gene inducer, in β‐thalassaemia intermedia and H b E /β‐thalassaemia

British journal of haematology, 2013-05, Vol.161 (4), p.587-593

2013

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research paper: alpha -Haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of beta -thalassaemia

British journal of haematology, 2006-06, Vol.133 (6), p.675-682

2006

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β-Thalassemia and βA globin gene haplotypes in Mexican mestizos

Human genetics, 1997-04, Vol.99 (4), p.498-500

1997

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Control of fetal hemoglobin: new insights emerging from genomics and clinical implications

Human molecular genetics, 2009-10, Vol.18 (R2), p.R216-R223

2009

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Anemia in the elderly: clinical implications and new therapeutic concepts

Haematologica (Roma), 2014-07, Vol.99 (7), p.1127-1130

2014

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Pain and opioid use after reversal of sickle cell disease following HLA‐matched sibling haematopoietic stem cell transplant

British journal of haematology, 2019-02, Vol.184 (4), p.690-693

2019

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Association between hemolysis and albuminuria in adults with sickle cell anemia

Haematologica (Roma), 2012-02, Vol.97 (2), p.201-205

2012

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Anemias. Hemoglobinopathies
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Recent Advances in the Treatment of Sickle Cell Disease

Tissue Iron Distribution Assessed by MRI in Patients with Iron Loading Anemias

Delayed haemolytic transfusion reaction in adults with sickle cell disease: a 5‐year experience

How we treat delayed haemolytic transfusion reactions in patients with sickle cell disease

Sickle cell nephropathy – a practical approach

World Sickle Cell Day 2016 : A time for appraisal

Interim assessment of liver damage in patients with sickle cell disease using new non‐invasive techniques

Interactions of an Anti-Sickling Drug with Hemoglobin in Red Blood Cells from a Patient with Sickle Cell Anemia

A randomized phase I/II trial of HQK‐1001, an oral fetal globin gene inducer, in β‐thalassaemia intermedia and HbE/β‐thalassaemia

Newborn screening for abnormal haemoglobins in Jamaica: Practical issues in an island programme

Haemoglobin Variant Screening in Jamaica: Meeting Student's Request

A Twins Heritability Study on Alpha Hemoglobin Stabilizing Protein (AHSP) Expression Variability

Effects of co-existing α-thalassaemia in sickle cell disease on hydroxycarbamide therapy and circulating nucleic acids

Renal iron load in sickle cell disease is influenced by severity of haemolysis

Outcome of adults with sickle cell disease admitted to critical care – experience of a single institution in the UK

α‐Haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of β‐thalassaemia

Outcome of children with sickle cell disease admitted to intensive care – a single institution experience

The associations between air quality and the number of hospital admissions for acute pain and sickle‐cell disease in an urban environment

A randomized phase I/II trial of HQK ‐1001, an oral fetal globin gene inducer, in β‐thalassaemia intermedia and H b E /β‐thalassaemia

research paper: alpha -Haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of beta -thalassaemia

β-Thalassemia and βA globin gene haplotypes in Mexican mestizos

Control of fetal hemoglobin: new insights emerging from genomics and clinical implications

Anemia in the elderly: clinical implications and new therapeutic concepts

Pain and opioid use after reversal of sickle cell disease following HLA‐matched sibling haematopoietic stem cell transplant

Association between hemolysis and albuminuria in adults with sickle cell anemia

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