comparison between the characteristics of Jamaican adults with normal hemo-globin and thote with sickle cell trait. Amer. J. Epid., 1969, 90: 236-243.—In surveys of representative samples of Jamaicans aged 3 5- 6 4 years living in rural and suburban communities, no significant differences in heights, weights, hema-tological indices, cardiothoracic ratios, blood pressures, glycosuria, proteinuria, parity or electrocardiographic abnormalities were apparent between 167 sub-jects with the sickle cell trait, AS, and 1,282 subjects with normal hemoglobin, AA. Older women with the trait had a significantly higher prevalence of bacte-riuria without other evidence of urinary tract pathology. The findings suggest that the trait is not appreciably ass...
The distribution of clinical features was examined in subjects with homozygous sickle cell (SS) dise...
Patients with sickle cell anemia (Hb SS) or sickle cell trait (Hb AS) may present several types of r...
Conflicting reports exist as to whether sickle cell trait is a risk factor for the progression of ne...
Hematocrit levels were studied in 8,581 male and 10,618 female Blacks aged 0-59 years, in Upstate Ne...
We performed hemoglobin electrophoresis in 30,400 apparently healthy black individuals in the Washin...
Based in the parish of Manchester in central Jamaica, the Manchester Project offered free detection ...
Albuminuria is a marker of glomerular damage in Sickle Cell Disease (SCD). In this study, we sought ...
THE incidence of the sickle cell trait among North American Negroes has been estimated from various ...
Sickle cell anemia is one of the first diseases to be understood at the molecular level. The amino a...
Sickle cell disease is the presence of two hemoglobin S alleles and results in sickle shaped red blo...
Heights and weights were measured in a cross-sectional study of 99 Jamaican children aged 2-13 years...
Objective: To compare the haematological and clinical features of homozygous sickle cell (SS) diseas...
The erythrocytes of certain human individuals undergo a reversible change in shape known as sickling...
AbstractSickle cell trait (SCT), the heterozygous state of the sickle hemoglobin beta globin gene (H...
OBJECTIVE:To investigate the role of haematological indices, socioeconomic status, and morbidity in ...
The distribution of clinical features was examined in subjects with homozygous sickle cell (SS) dise...
Patients with sickle cell anemia (Hb SS) or sickle cell trait (Hb AS) may present several types of r...
Conflicting reports exist as to whether sickle cell trait is a risk factor for the progression of ne...
Hematocrit levels were studied in 8,581 male and 10,618 female Blacks aged 0-59 years, in Upstate Ne...
We performed hemoglobin electrophoresis in 30,400 apparently healthy black individuals in the Washin...
Based in the parish of Manchester in central Jamaica, the Manchester Project offered free detection ...
Albuminuria is a marker of glomerular damage in Sickle Cell Disease (SCD). In this study, we sought ...
THE incidence of the sickle cell trait among North American Negroes has been estimated from various ...
Sickle cell anemia is one of the first diseases to be understood at the molecular level. The amino a...
Sickle cell disease is the presence of two hemoglobin S alleles and results in sickle shaped red blo...
Heights and weights were measured in a cross-sectional study of 99 Jamaican children aged 2-13 years...
Objective: To compare the haematological and clinical features of homozygous sickle cell (SS) diseas...
The erythrocytes of certain human individuals undergo a reversible change in shape known as sickling...
AbstractSickle cell trait (SCT), the heterozygous state of the sickle hemoglobin beta globin gene (H...
OBJECTIVE:To investigate the role of haematological indices, socioeconomic status, and morbidity in ...
The distribution of clinical features was examined in subjects with homozygous sickle cell (SS) dise...
Patients with sickle cell anemia (Hb SS) or sickle cell trait (Hb AS) may present several types of r...
Conflicting reports exist as to whether sickle cell trait is a risk factor for the progression of ne...