Inherited haemoglobin disorders: an increasing global health problem
about
How malaria has affected the human genome and what human genetics can teach us about malariaEvolutionary and historical aspects of the burden of malaria.Hb E/beta-thalassaemia: a common & clinically diverse disorderPrecipitating factors and targeted therapies in combating the perils of sickle cell disease--- A special nutritional considerationClinical Management of Priapism: A ReviewBeta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa?Oxidative stress and β-thalassemic erythroid cells behind the molecular defectGuidelines for screening, diagnosis and management of hemoglobinopathiesThe influence of vitamin A supplementation on iron statusHemoglobin variants: biochemical properties and clinical correlatesProfiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmesGlobal migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000.Global, regional, and national trends in haemoglobin concentration and prevalence of total and severe anaemia in children and pregnant and non-pregnant women for 1995-2011: a systematic analysis of population-representative data.Perspectives in Genetics and Sickle Cell Disease Prevention in Africa: Beyond the Preliminary Data from CameroonAnalysis of survival data in thalassemia patients in Shiraz, IranAfrican meningitis belt pneumococcal disease epidemiology indicates a need for an effective serotype 1 containing vaccine, including for older children and adultsPopulation hemoglobin mean and anemia prevalence in Papua New Guinea: new metrics for defining malaria endemicity?Inferring linkage disequilibrium from non-random samples.Consulting communities on feedback of genetic findings in international health research: sharing sickle cell disease and carrier information in coastal Kenya.The prevalence of thalassemia in mainland China: evidence from epidemiological surveysHemoglobinopathies: a longitudinal study over four decades.Mutation analysis of β-thalassemia in East-Western Indian population: a recent molecular approach.Primate malarias: Diversity, distribution and insights for zoonotic Plasmodium.Psychosocial impact of sickle cell disorder: perspectives from a Nigerian settingSickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival.Molecular epidemiological characterization and health burden of thalassemia in Jiangxi Province, P. R. China.A call for policy action in sub-Saharan Africa to rethink diagnostics for pregnancy affected by sickle cell disease: differential views of medical doctors, parents and adult patients predict value conflicts in Cameroon.Thalassemia and hemoglobinopathies in an ethnic minority group in Central Vietnam: implications to health burden and relationship between two ethnic minority groups.Pulmonary hypertension in hemolytic disorders: pulmonary vascular disease: the global perspective.Mapping the risk of anaemia in preschool-age children: the contribution of malnutrition, malaria, and helminth infections in West AfricaSickle cell disease in areas of immigration of high-risk populations: a low cost and reproducible method of screening in northern ItalyEvaluation of married haemoglobinopathic carrier couples for prevention of haemoglobinopathic birthsDetection of sickle cell hemoglobin in Haiti by genotyping and hemoglobin solubility testsHypertransfusion therapy in sickle cell disease in NigeriaIron overload cardiomyopathy: better understanding of an increasing disorder.High prevalence of thalassemia in migrant populations in Guangdong Province, ChinaUse of glucometer and fasting blood glucose as screening tools for diabetes mellitus type 2 and glycated haemoglobin as clinical reference in rural community primary care settings of a middle income country.Identification and key management of non-transfusion-dependent thalassaemia patients: not a rare but potentially under-recognised conditionPreconceptional ancestry-based carrier couple screening for cystic fibrosis and haemoglobinopathies: what determines the intention to participate or not and actual participation?
P2860
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P2860
Inherited haemoglobin disorders: an increasing global health problem
description
2001 nî lūn-bûn
@nan
2001 թուականին հրատարակուած գիտական յօդուած
@hyw
2001 թվականին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Inherited haemoglobin disorders: an increasing global health problem
@ast
Inherited haemoglobin disorders: an increasing global health problem
@en
Inherited haemoglobin disorders: an increasing global health problem
@nl
type
label
Inherited haemoglobin disorders: an increasing global health problem
@ast
Inherited haemoglobin disorders: an increasing global health problem
@en
Inherited haemoglobin disorders: an increasing global health problem
@nl
prefLabel
Inherited haemoglobin disorders: an increasing global health problem
@ast
Inherited haemoglobin disorders: an increasing global health problem
@en
Inherited haemoglobin disorders: an increasing global health problem
@nl
P3181
P1476
Inherited haemoglobin disorders: an increasing global health problem
@en
P2093
D J Weatherall
P304
P3181
P407
P577
2001-01-01T00:00:00Z