Results 341 to 350 of about 20,445,864 (375)
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Hemoglobins S and C in Upper Volta
Human Genetics, 1984We have studied the incidence of hemoglobinopathies in 1059 individuals in Upper Volta. We have found that this population has a high frequency of HbS and HbC and alpha-thalassemia. The gene frequency of HbS was high (0.1 for the beta s gene) in the arid Sahel portion of Upper Volta accompanied by a lower frequency for HbC (0.05 for the beta c gene ...
Dominique Labie +4 more
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Compound Heterozygosity for Hemoglobin C and Hemoglobin Korle-Bu
Laboratory Hematology, 2008We describe a case of compound heterozygosity for hemoglobin C (beta6 Glu-->Lys) and hemoglobin Korle-Bu (beta73 Asp-->Asn). To our knowledge, this is the third case report of this unusual hemoglobin genotype, and the first to integrate data from cation exchange high-performance liquid chromatography, hemoglobin electrophoresis, and beta-globin gene ...
Andrew N. Young +2 more
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Hemoglobin C in association with hereditary persistence of fetal hemoglobin
Postgraduate Medicine, 1987Hemoglobin C and hereditary persistence of fetal hemoglobin (HPFH) are an uncommon combination of hemoglobinopathies. Several tests are needed to verify this condition, among them hemoglobin electrophoresis and Kleihauer-Betke staining of a peripheral blood smear.
J. A. Lynch +4 more
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Hemoglobin C disease in infancy and childhood☆☆☆★★★
The Journal of Pediatrics, 1994We reviewed the clinical course, physical findings, and hematologic values in 16 pediatric patients with hemoglobin C disease, all but one identified by a newborn hemoglobinopathy screening program. The patients had a few symptoms or physical findings. Height and weight percentiles were normal.
William H. Schultz +3 more
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Priapism Associated with Hemoglobin C Trait
Journal of Urology, 2002Priapism constitutes a urological emergency in which alterations to the normal physiological process leading to penile erection result in a prolonged painful erection. One hemoglobinopathy, sickle cell anemia, is linked with priapism in 11% of cases.1 Hemoglobin C is an abnormal hemoglobin distinct from hemoglobin S, which is found in sickle cell ...
Raymond A. Costabile +2 more
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American Journal of Hematology, 1976
AbstractThe improved microchromatographic procedure for the detection of Hb‐S and/or Hb‐C in cord blood at birth (Schroeder et al.: J. Lab Clin Med 86:528‐532, 1975) as well as a modification thereof may also be used for the quantitative determination of Hb‐F in the presence of Hb‐S and/or Hb‐C. However, Hb‐A interferes and must be absent.
Joan Balog Shelton +6 more
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AbstractThe improved microchromatographic procedure for the detection of Hb‐S and/or Hb‐C in cord blood at birth (Schroeder et al.: J. Lab Clin Med 86:528‐532, 1975) as well as a modification thereof may also be used for the quantitative determination of Hb‐F in the presence of Hb‐S and/or Hb‐C. However, Hb‐A interferes and must be absent.
Joan Balog Shelton +6 more
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Critical Care Medicine, 1996
OBJECTIVES a) To determine whether isovolemic exchange transfusion with cell-free, bovine fumaryl beta beta-crosslinked hemoglobin results in a different pattern of regional blood flow distribution than transfusion with a poor oxygen-carrying, colloidal ...
J. Ulatowski +5 more
semanticscholar +1 more source
OBJECTIVES a) To determine whether isovolemic exchange transfusion with cell-free, bovine fumaryl beta beta-crosslinked hemoglobin results in a different pattern of regional blood flow distribution than transfusion with a poor oxygen-carrying, colloidal ...
J. Ulatowski +5 more
semanticscholar +1 more source
Homozygous hemoglobin C disease
The American Journal of Medicine, 1955Abstract The clinical features of a case of homozygous hemoglobin C disease have been described. This condition is characterized by a mild normochromic, normocytic anemia, many target cells, and a characteristic electrophoretic hemoglobin pattern. The mean red cell life span of the patient's cells in a normal recipient was found to be forty-two days ...
E.D. Thomas, A.G. Motulsky, D.H. Walters
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Pediatrics, 1953
A case of "homozygous" type "c" hemoglobin is reported in a Negro child. Although the patient was clinically free of hernolytic disease, the peripheral blood showed numerous target cells, and a compensated hemolytic process was demonstrated. Clinical and theoretic implications of the condition are discussed.
Theodore H. Spaet +2 more
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A case of "homozygous" type "c" hemoglobin is reported in a Negro child. Although the patient was clinically free of hernolytic disease, the peripheral blood showed numerous target cells, and a compensated hemolytic process was demonstrated. Clinical and theoretic implications of the condition are discussed.
Theodore H. Spaet +2 more
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Molecular characterization of hemoglobin C in sicily
American Journal of Hematology, 1992AbstractAnalysis of polymorphisms of the β‐globin gene cluster was performed on 12 families and on one unrelated individual of Sicilian origin who carried hemoglobin C (Hb C). Two different haplotypes were found in association with βc Sicilian alleles, corresponding to haplotypes I and II previously described in American blacks.
Gino Schilirò +6 more
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