World distribution, population genetics, and health burden of the hemoglobinopathies.
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Hematopoietic stem cell transplantation in thalassemia and sickle cell anemiaHemoglobin variants: biochemical properties and clinical correlatesClinical laboratory reference values amongst children aged 4 weeks to 17 months in Kilifi, Kenya: A cross sectional observational study.Evaluation of staff performance and interpretation of the screening program for prevention of thalassemia.Thalassemia and hemoglobinopathies in an ethnic minority group in Central Vietnam: implications to health burden and relationship between two ethnic minority groups.Sickle cell disease in areas of immigration of high-risk populations: a low cost and reproducible method of screening in northern ItalyAnemia and growthPrevalence of common hemoglobin variants in an afro-descendent Ecuadorian populationRed blood cell indices and prevalence of hemoglobinopathies and glucose 6 phosphate dehydrogenase deficiencies in male Tanzanian residents of Dar es Salaam.Effect of early and current Helicobacter pylori infection on the risk of anaemia in 6.5-year-old Ethiopian childrenSpectrum of alpha-globin gene mutations among premarital Baluch couples in southeastern Iran.Intestine-specific Disruption of Hypoxia-inducible Factor (HIF)-2α Improves Anemia in Sickle Cell Disease.The hemoglobin E thalassemias.High Incidence of Malaria Along the Sino-Burmese Border Is Associated With Polymorphisms of CR1, IL-1A, IL-4R, IL-4, NOS, and TNF, But Not With G6PD Deficiency.EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.Tipping the balance: Haemoglobinopathies and the risk of diabetes.Thalassemia and sickle cell anemia in Swedish immigrants: Genetic diseases have become global.Clinical manifestations of α-thalassemia.Novel one-step multiplex PCR-based method for HLA typing and preimplantational genetic diagnosis of β-ThalassemiaPostnatal Prediction of Gestational Age Using Newborn Fetal Hemoglobin Levels.Mechanism-driven phase I translational study of trifluoperazine in adults with sickle cell disease.Prevalence of deletional alpha thalassemia and sickle gene in a tribal dominated malaria endemic area of eastern India.β-Thalassemia Distribution in the Old World: an Ancient Disease Seen from a Historical Standpoint.Red blood cell components: time to revisit the sources of variability.Simple and Easy to Perform Preimplantation Genetic Diagnosis for β-thalassemia Major Using Combination of Conventional and Fluorescent Polymerase Chain Reaction.Preimplantation genetic diagnosis, an alternative to conventional prenatal diagnosis of the hemoglobinopathies.Advances in technologies for screening and diagnosis of hemoglobinopathies.Enhancer biology and enhanceropathies.β-globin genes: mutation hot-spots in the global thalassemia belt.A journey in science: early lessons from the hemoglobin fieldHBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers.Epidemiology of Hemoglobinopathies in the Huzhou Region, Zhejiang Province, Southeast China.To condition or not to condition-That is the question: The evolution of nonmyeloablative conditions for transplantation.Laboratory diagnosis of thalassemia.Clinically-oriented proteomic investigation of sickle cell disease: Opportunities and challenges.The G6PD flow-cytometric assay is a reliable tool for diagnosis of G6PD deficiency in women and anaemic subjects.Plasmodium falciparum infection in febrile Congolese children: prevalence of clinical malaria 10 years after introduction of artemisinin-combination therapies.The role of the red blood cell in host defence against falciparum malaria: an expanding repertoire of evolutionary alterations.Molecular basis of β thalassemia and potential therapeutic targets.The Association between Educational Attainment and Patterns of Emergency Department Utilization among Adults with Sickle Cell Disease.
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World distribution, population genetics, and health burden of the hemoglobinopathies.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
World distribution, population genetics, and health burden of the hemoglobinopathies.
@en
type
label
World distribution, population genetics, and health burden of the hemoglobinopathies.
@en
prefLabel
World distribution, population genetics, and health burden of the hemoglobinopathies.
@en
P2860
P1476
World distribution, population genetics, and health burden of the hemoglobinopathies.
@en
P2093
David J Weatherall
Thomas N Williams
P2860
P304
P356
10.1101/CSHPERSPECT.A011692
P577
2012-09-01T00:00:00Z