Results 241 to 250 of about 412,948 (294)

Radioimmunoassay for Abnormal Hemoglobins

Science, 1977
A sensitive and specific radioimmunoassay has been developed for the identification or quantification of the human hemoglobin variants S, C, D-Los Angeles, E, G Philadelphia, Russ, O Arab, Beograd, J Paris I, G San Jose, Q Iran, Korle Bu, and F Malta I.
F A, Garver, M B, Baker, C S, Jones, M, Gravely, G, Altay, T H, Huisman   +5 more
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ABNORMAL HEMOGLOBINS: LABORATORY METHODS

Hemoglobin, 2001
Laboratory methods allowing the detection and characterization of hemoglobin variants are reviewed. Protein chemistry techniques such as isoelectrofocusing, electrophoreses under various experimental conditions, cation exchange and reversed phase high performance liquid chromatography, are the most frequently used for the detection of variants.
H, Wajcman, C, Préhu, J, Bardakdjian-Michau, D, Promé, J, Riou, C, Godart, M, Mathis, D, Hurtrel, F, Galactéros   +8 more
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Normal and Abnormal Human Hemoglobins

1963
Publisher Summary This chapter reviews that spectacular progress has been made in the recognition and study of biological differences between hemoglobin types. Many aspects of variations in hemoglobins such as the worldwide distribution of human hemoglobin types and their epidemiologic implications, animal hemoglobin types, and others have not been ...
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ABNORMAL HEMOGLOBINS

The American Journal of the Medical Sciences, 1961
Summary and ConclusionsSickle cell trait can be separated from hemoglobin S-C disease, S-thalassemia, and even sickle cell anemia only on the basis of careful hematologic and electrophoretic studies, even after necropsy has been performed.
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Abnormal hemoglobins in the Negroes of Surinam

The American Journal of Medicine, 1958
Abstract 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, J, ELDERKIN, I, GUICHIRIT, H W, BROWN, H M, RANNEY   +4 more
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The Hematuria of Abnormal Hemoglobin Diseases

Archives of Surgery, 1955
The 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 Acta
Hemoglobin (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, Muhammad, Idrees Khan, Saud, Shah, Youli, Tian, Genhan, Zha, Liuyin, Fan, Qiang, Zhang, Chengxi, Cao   +7 more
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Abnormal Hemoglobins in Gurkhas

Hemoglobin, 1979
S C, Gupta, Y K, Goorah, T N, Mehrotra, D, Bisht   +3 more
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Proliferation of Human Abnormal Hemoglobins

Annals of Internal Medicine, 1969
Excerpt 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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Nomenclature of Abnormal Hemoglobins

American Journal of Clinical Pathology, 1965
M J, PICKETT, C R, MANCLARK
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