Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene.
about
Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart StudyMutations and polymorphisms in hemoglobin genes and the risk of pulmonary hypertension and death in sickle cell diseaseEffects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell traitGenomic approaches to identifying targets for treating β hemoglobinopathiesNegative health implications of sickle cell trait in high income countries: from the football field to the laboratoryGenetic determinants of haemolysis in sickle cell anaemia.Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia.Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.Alpha thalassaemia in tribal communities of coastal Maharashtra, IndiaEffect of red blood cell variants on childhood malaria in Mali: a prospective cohort study.Alpha thalassemia among sickle cell anaemia patients in Kampala, Uganda.Genetic modifiers of sickle cell diseaseInteraction between Hb SS and alpha thalassemia (3.7 kb deletion): a familial study.Sickle Cell Trait Increases Red Blood Cell Storage Hemolysis and Post-Transfusion Clearance in MiceAlpha-thalassaemia and response to hydroxyurea in sickle cell anaemia.Minireview: Genetic basis of heterogeneity and severity in sickle cell disease.Hydroxyurea in Sickle Cell Disease: Our Experience in Western India.Knowledge insufficient: the management of haemoglobin SC disease.Hemolysis-associated priapism in sickle cell diseasePrevalence of β(S)-globin gene haplotypes, α-thalassemia (3.7 kb deletion) and redox status in patients with sickle cell anemia in the state of Paraná, Brazil.Some observations on the measurement of haemoglobin A2 and S percentages by high performance liquid chromatography in the presence and absence of alpha thalassaemia.Can Trimodal Distribution of HbS Levels in Sickle Cell Traits Be Used To Predict the Associated Alpha-Thalassemia For Screening Cases in Central India?The spectrum of sickle hemoglobin-related nephropathy: from sickle cell disease to sickle trait.Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.
P2860
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P2860
Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年学术文章
@wuu
1986年学术文章
@zh-cn
1986年学术文章
@zh-hans
1986年学术文章
@zh-my
1986年学术文章
@zh-sg
1986年學術文章
@yue
1986年學術文章
@zh
1986年學術文章
@zh-hant
name
Alpha-thalassemia in blacks: g ...... th the sickle hemoglobin gene.
@en
Alpha-thalassemia in blacks: g ...... th the sickle hemoglobin gene.
@nl
type
label
Alpha-thalassemia in blacks: g ...... th the sickle hemoglobin gene.
@en
Alpha-thalassemia in blacks: g ...... th the sickle hemoglobin gene.
@nl
prefLabel
Alpha-thalassemia in blacks: g ...... th the sickle hemoglobin gene.
@en
Alpha-thalassemia in blacks: g ...... th the sickle hemoglobin gene.
@nl
P1433
P1476
Alpha-thalassemia in blacks: g ...... ith the sickle hemoglobin gene
@en
P2093
M H Steinberg
S H Embury
P304
P407
P577
1986-11-01T00:00:00Z