Co-inheritance of alpha+-thalassaemia and sickle trait results in specific effects on haematological parameters
about
The effect of alpha+-thalassaemia on the incidence of malaria and other diseases in children living on the coast of KenyaIncreased microerythrocyte count in homozygous alpha(+)-thalassaemia contributes to protection against severe malarial anaemiaA novel functional variant in the stem cell growth factor promoter protects against severe malarial anemiaAssociation between Fcγ receptor IIA, IIIA and IIIB genetic polymorphisms and susceptibility to severe malaria anemia in children in western Kenya.Haplotype of non-synonymous mutations within IL-23R is associated with susceptibility to severe malaria anemia in a P. falciparum holoendemic transmission area of KenyaNutritional status of young children with inherited blood disorders in western Kenya.Iron deficiency and acute seizures: results from children living in rural Kenya and a meta-analysisFunctional haplotypes of Fc gamma (Fcγ) receptor (FcγRIIA and FcγRIIIB) predict risk to repeated episodes of severe malarial anemia and mortality in Kenyan childrenRacial variation in the relationship of anemia with mortality and mobility disability among older adults.β-Globin chain abnormalities with coexisting α-thalassemia mutations.Partitioning regulatory mechanisms of within-host malaria dynamics using the effective propagation number.The burden and consequences of inherited blood disorders among young children in western Kenya.A Number of Cases in Iran Presenting with Coinheritance of Hemoglobin-H Disease and Beta-Thalassemia Minor.Sickle Cell Trait Causing Splanchnic Venous Thrombosis.Sickle-cell and alpha-thalassemia traits resulting in non-atherosclerotic myocardial infarction: Beyond coincidence?Cut-Off Values of Hematologic Parameters to Predict the Number of Alpha Genes Deleted in Subjects with Deletional Alpha Thalassemia.Microbiology. Quantifying malaria dynamics within the host.Laboratory parameters provided by Advia 2120 analyser identify structural haemoglobinopathy carriers and discriminate between Hb S trait and Hb C trait.Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.Human candidate gene polymorphisms and risk of severe malaria in children in Kilifi, Kenya: a case-control association studyAssociations between erythrocyte polymorphisms and risks of uncomplicated and severe malaria in Ugandan children: A case control studyFemales of HbAS genotype have reduced concentration of the malaria protective deoxyhemoglobin S than males
P2860
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P2860
Co-inheritance of alpha+-thalassaemia and sickle trait results in specific effects on haematological parameters
description
2006 nî lūn-bûn
@nan
2006 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Co-inheritance of alpha+-thala ...... s on haematological parameters
@ast
Co-inheritance of alpha+-thala ...... s on haematological parameters
@en
type
label
Co-inheritance of alpha+-thala ...... s on haematological parameters
@ast
Co-inheritance of alpha+-thala ...... s on haematological parameters
@en
prefLabel
Co-inheritance of alpha+-thala ...... s on haematological parameters
@ast
Co-inheritance of alpha+-thala ...... s on haematological parameters
@en
P2093
P2860
P1476
Co-inheritance of alpha+-thala ...... s on haematological parameters
@en
P2093
Alexander Macharia
Jedidah Mwacharo
Sammy Wambua
Sophie Uyoga
P2860
P304
P356
10.1111/J.1365-2141.2006.06006.X
P407
P577
2006-04-01T00:00:00Z