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Sickle Cell Anemia and Hearing
Annals of Otology, Rhinology & Laryngology, 1980The present investigation examined the effects of sickle cell anemia on threshold hearing. The study included 43 homozygous sickle cell anemia patients, ages 7–18 years, and 23 age-matched controls with documented normal hemoglobin. Both the study and control groups received otologic and audiologic examinations. Bilaterally normal hearing was found in
E M, Friedman +3 more
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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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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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