Concurrent sickle cell anemia and alpha-thalassemia. Effect on pathological properties of sickle erythrocytes
about
Red cell membrane: past, present, and futureEffects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell traitbeta(S)-Globin gene cluster haplotypes in the West Bank of Palestine.Haptoglobin, alpha-thalassaemia and glucose-6-phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania.Density-based separation in multiphase systems provides a simple method to identify sickle cell diseaseEffect of human beta (s)-globin chains on cellular properties of red cells from beta-thalassemic mice.Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease.Developing treatment for sickle cell disease.Evaluation of a density-based rapid diagnostic test for sickle cell disease in a clinical setting in Zambia.Disorders of red cell membrane.Prospective study of sickle cell trait and venous thromboembolism incidenceMalaria induces anemia through CD8+ T cell-dependent parasite clearance and erythrocyte removal in the spleen.Blood thixotropy in patients with sickle cell anaemia: role of haematocrit and red blood cell rheological properties.Alpha thalassemia among sickle cell anaemia patients in Kampala, Uganda.Hematological and Genetic Predictors of Daytime Hemoglobin Saturation in Tanzanian Children with and without Sickle Cell Anemia.Analysis of hemoglobin electrophoresis results and physicians investigative practices in Saudi Arabia.Differences in the clinical and genotypic presentation of sickle cell disease around the world.Modifier genes in Mendelian disorders: the example of hemoglobin disorders.Advances in understanding the pathogenesis of cerebrovascular vasculopathy in sickle cell anaemia.From the bench to the field in low-cost diagnostics: two case studies.Knowledge insufficient: the management of haemoglobin SC disease.Intravascular hemolysis and the pathophysiology of sickle cell disease.Hemolysis-associated priapism in sickle cell diseaseVariants in the non-coding region of the TLR2 gene associated with infectious subphenotypes in pediatric sickle cell anemia.Red blood cell aggregation, aggregate strength and oxygen transport potential of blood are abnormal in both homozygous sickle cell anemia and sickle-hemoglobin C disease.Realizing effectiveness across continents with hydroxyurea: Enrollment and baseline characteristics of the multicenter REACH study in Sub-Saharan Africa.Measuring Deformability and Red Cell Heterogeneity in Blood by Ektacytometry.Alpha-thalassaemia promotes frequent vaso-occlusive crises in children with sickle cell anaemia through haemorheological changes.Age-dependent changes in the membrane surface area: sickle red blood cell volume may account for differential clinical effects of coinherited α thalassemia on sickle cell anemia.Vom Labortisch zur Feldforschung: zwei Fallstudien kostengünstiger Diagnostik
P2860
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P2860
Concurrent sickle cell anemia and alpha-thalassemia. Effect on pathological properties of sickle erythrocytes
description
1984 nî lūn-bûn
@nan
1984 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1984 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1984年の論文
@ja
1984年論文
@yue
1984年論文
@zh-hant
1984年論文
@zh-hk
1984年論文
@zh-mo
1984年論文
@zh-tw
1984年论文
@wuu
name
Concurrent sickle cell anemia ...... perties of sickle erythrocytes
@ast
Concurrent sickle cell anemia ...... perties of sickle erythrocytes
@en
Concurrent sickle cell anemia ...... perties of sickle erythrocytes
@nl
type
label
Concurrent sickle cell anemia ...... perties of sickle erythrocytes
@ast
Concurrent sickle cell anemia ...... perties of sickle erythrocytes
@en
Concurrent sickle cell anemia ...... perties of sickle erythrocytes
@nl
prefLabel
Concurrent sickle cell anemia ...... perties of sickle erythrocytes
@ast
Concurrent sickle cell anemia ...... perties of sickle erythrocytes
@en
Concurrent sickle cell anemia ...... perties of sickle erythrocytes
@nl
P2093
P2860
P356
P1476
Concurrent sickle cell anemia ...... perties of sickle erythrocytes
@en
P2093
P2860
P304
P356
10.1172/JCI111181
P407
P577
1984-01-01T00:00:00Z