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The Inheritance of Sickle Cell Anemia
Science, 1949IF A DROP OF BLOOD is collected from each member of a randomly assembled series of American Negroes and sealed under a cover slip with vaseline, to be observed at intervals up to 72 hours, in the case of about 8 percent of the individuals composing the series a high proportion of the erythrocytes will be observed to assume various bizarre oat, sickle ...
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JAMA: The Journal of the American Medical Association, 1963
Four patients presenting unusual manifestations of sickle cell anemia were studied. Clinical variants were age, habitus, and pregnancy. In some cases, these features were so atypical as to suggest disease entities other than sickle cell anemia and obscure the diagnosis.
R C, GAUSE +3 more
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Four patients presenting unusual manifestations of sickle cell anemia were studied. Clinical variants were age, habitus, and pregnancy. In some cases, these features were so atypical as to suggest disease entities other than sickle cell anemia and obscure the diagnosis.
R C, GAUSE +3 more
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Sickle Cell Anemia and Pregnancy
Postgraduate Medicine, 1952A study was made of 18 cases of sickle cell anemia, 4 of which were complicated by pregnancy. These 4 cases are reported in detail, including the postmortem findings for one of them. The frequency of the various symptoms of sickle cell anemia and a summary of the cases complicated by pregnancy are presented in tabulated form.
R, CHARET, R, WALTMAN, H, FERNBACH
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Cholecystectomy in Sickle Cell Anemia
Archives of Pediatrics & Adolescent Medicine, 1989Sir.—In the July 1988 issue ofAJDC, Malone and Werlin1reported the resuits of preoperative transfusion before elective cholecystectomy at the time of diagnosis of cholelithiasis in children with sickle cell anemia. Our own practice supports the conclusions of this study. From 1976 to 1988, 240 children have been seen at the sickle cell clinic.
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Splenectomy in Sickle Cell Anemia
Archives of Internal Medicine, 1970Sickle cell anemia is a severe hemolytic disease caused by a congenital hemoglobin defect for which there is no treatment. Clinical management of patients with the disorder is purely symptomatic, and a "hands off" policy regarding transfusion is best.
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Pseudomoyamoya in sickle cell anemia
Surgical Neurology, 1982Sickle cell (drepanocytic) anemia is a hereditary blood disease occurring very rarely in Mexico. A 13-year-old Mexican boy with sickle cell anemia eventually died of a cerebrovascular accident of the brain stem, as shown by computerized tomography (CT).
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TREATMENT OF SICKLE CELL ANEMIA
Archives of Internal Medicine, 1954SICKLE cell anemia was described first by Herrick in 1910. 1 Since then, surveys of Negroes in the United States have revealed the incidence of the symptomless sickle cell trait to be about 9% and incidence of sickle cell anemia to be about 2.25 per thousand.
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Thrombocytosis in Sickle Cell Anemia
Archives of Pediatrics & Adolescent Medicine, 1997In the July 1996 issue of theArchives, Quintana et al1described an adolescent girl with sickle cell anemia and extreme thrombocytosis (platelet count, 2×1012/L). We2,3have also described thrombocytosis in patients with sickle cell anemia; their platelet counts were higher than those in children who underwent splenectomy, but did not exceed 106/L.
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