Results 151 to 160 of about 4,456 (190)
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Abnormal hemoglobins in the Negroes of Surinam
The American Journal of Medicine, 1958Abstract 1. 1. A study of the incidence of abnormal hemoglobins among the Djuka population of Surinam revealed an incidence of sickle cell hemoglobin of 15 per cent and an incidence of hemoglobin C of 3 per cent. Two cases interpreted as sickle cell-thalassemia disease indicated the probable presence of the gene for thalassemia in the Djukas. The
C, LIACHOWITZ +4 more
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The Hematuria of Abnormal Hemoglobin Diseases
Archives of Surgery, 1955The property of the red blood cell to sickle is a manifestation of abnormal molecular arrangement of that cell's hemoglobin. This was established by Pauling and co-workers in 1949. 1 Since then, other abnormal hemoglobins have been discovered by electrophoretic methods.
S M, GOLDMAN, A Z, CHAPMAN, R R, CROSS
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Diagnosis and screening of abnormal hemoglobins
Clinica Chimica ActaHemoglobin (Hb) abnormalities, such as thalassemia and structural Hb variants, are among the most prevalent inherited diseases and are associated with significant mortality and morbidity worldwide. However, there were not comprehensive reviews focusing on different clinical analytical techniques, research methods and artificial intelligence (AI) used ...
Ali, Sani +7 more
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Nomenclature of Abnormal Hemoglobins
American Journal of Clinical Pathology, 1965M J, PICKETT, C R, MANCLARK
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Proliferation of Human Abnormal Hemoglobins
Annals of Internal Medicine, 1969Excerpt As investigators have become more peripatetic, primitive tribesmen such as the Bantus and Bushmen in Africa have undergone more careful scrutiny.
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Structural analysis on the abnormal elongated hemoglobin “hemoglobin Geneva”
Nanomedicine: Nanotechnology, Biology and Medicine, 2005Hemoglobin variants in which a frameshift results in chain elongation are not common. Hemoglobin Geneva (HbGeneva) is an unstable hemologin with abnormal elongation. This hemoglobinopathy is known for its high instability. Concerning the pathogenesis of HbGeneva, the data indicate a change in codon 114 from CTG (Leu) to -GG that results in a frame ...
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Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme, 1969
S, Shibata, I, Iuchi
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S, Shibata, I, Iuchi
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Prevalence of Beta-Thalassemia Trait and Abnormal Hemoglobins in the Province of Adıyaman, Turkey
Pediatric Hematology and Oncology, 2012Ahmet Genc +2 more
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