The challenge of haemoglobinopathies in resource-poor countries

Optimal management of β thalassaemia intermedia

(2011) Ali T. Taher et al.   BRITISH JOURNAL OF HAEMATOLOGY

Mortality in Sickle Cell Anemia in Africa: A Prospective Cohort Study in Tanzania

(2011) Julie Makani et al.   PLoS One

Emerging insights in the management of hemoglobin E beta thalassemia

(2010) Nancy F. Olivieri et al.   Annals of the New York Academy of Sciences

The inherited diseases of hemoglobin are an emerging global health burden

(2010) D. J. Weatherall   BLOOD

Genetic variation and susceptibility to infection: the red cell and malaria

(2010) D. J. Weatherall   BRITISH JOURNAL OF HAEMATOLOGY

Epidemiology of β-thalassaemia in Western India: mapping the frequencies and mutations in sub-regions of Maharashtra and Gujarat

(2010) Roshan Colah et al.   BRITISH JOURNAL OF HAEMATOLOGY

The importance of micromapping the gene frequencies for the common inherited disorders of haemoglobin

(2010) David J. Weatherall   BRITISH JOURNAL OF HAEMATOLOGY

Large scale screening for haemoglobin disorders in southern Vietnam: implications for avoidance and management

(2010) Sean O’Riordan et al.   BRITISH JOURNAL OF HAEMATOLOGY

Global distribution of the sickle cell gene and geographical confirmation of the malaria hypothesis

(2010) Frédéric B. Piel et al.   Nature Communications

Bacteraemia in Kenyan children with sickle-cell anaemia: a retrospective cohort and case–control study

(2009) Thomas N Williams et al.   LANCET

Epistatic interactions between genetic disorders of hemoglobin can explain why the sickle-cell gene is uncommon in the Mediterranean

(2009) Bridget S. Penman et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Global epidemiology of haemoglobin disorders and derived service indicators

(2008) Bernadette Modell   BULLETIN OF THE WORLD HEALTH ORGANIZATION

Newborn screening for sickle cell disease in the Republic of Benin

(2008) M C Rahimy et al.   JOURNAL OF CLINICAL PATHOLOGY