Results 211 to 220 of about 71,196 (274)
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Postgraduate Medicine, 1952
For general practitioners, as well as specialists, this department offers the latest, proved methods of treatment of conditions encountered in an average practice. It is not, of course, intended to present these discussions as the only acceptable therapeutic procedures to be used, but rather to offer simple regimens and recommendations based on the ...
G W, JAMES, W B, PORTER
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For general practitioners, as well as specialists, this department offers the latest, proved methods of treatment of conditions encountered in an average practice. It is not, of course, intended to present these discussions as the only acceptable therapeutic procedures to be used, but rather to offer simple regimens and recommendations based on the ...
G W, JAMES, W B, PORTER
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Sickle cell anemia and pregnancy
American Journal of Obstetrics and Gynecology, 1949Abstract The present study is a review of eleven cases of sickle cell anemia associated with pregnancy observed on the Obstetrical Service of the Johns Hopkins Hospital over a 20-year period (1927–1947). No deaths occurred in these eleven mothers during the period of the pregnancy or puerperium.
G W, ANDERSON, T, BUSBY
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Enuresis in Sickle Cell Anemia
Archives of Pediatrics & Adolescent Medicine, 1967IT IS WELL recognized that patients with sickle cell disease have hyposthenuria. 1 This hyposthenuria results in the excretion of increased volumes of urine during a 24-hour period. It has been our impression that this polyuria results in an increased incidence of enuresis among children with sickle cell anemia.
G, Suster, F A, Oski
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American Journal of Diseases of Children, 1923
J. B. Herrick, 1 in 1910, reported a peculiar dyscrasia characterized by severe anemia, with the occurrence in the blood of elongated and sickle-shaped erythrocytes. Three instances of this condition have since been described, one by R. E. Washburn; 2 one by Cook and Myer, 3 and one by V. R. Mason. 4 Emmel 5 further studied the blood of Cook and Myer's
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J. B. Herrick, 1 in 1910, reported a peculiar dyscrasia characterized by severe anemia, with the occurrence in the blood of elongated and sickle-shaped erythrocytes. Three instances of this condition have since been described, one by R. E. Washburn; 2 one by Cook and Myer, 3 and one by V. R. Mason. 4 Emmel 5 further studied the blood of Cook and Myer's
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Annals of Internal Medicine, 1978
Excerpt To the editor: The "natural history" of sickle cell anemia in Saudi Arabs (Ann Intern Med88:1-6, 1978) is certainly different from the disease as we see it in the United States but not as d...
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Excerpt To the editor: The "natural history" of sickle cell anemia in Saudi Arabs (Ann Intern Med88:1-6, 1978) is certainly different from the disease as we see it in the United States but not as d...
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Issues in Comprehensive Pediatric Nursing, 1980
Sickle-cell anemia is a genetic disorder characterized by abnormal hemoglobin. One out of every 500 black children in the United States is affected by this disease. Eight to ten percent of the black population has the sickle-cell trait. While other hemoglobinopathies have been identified that also produce erythrocyte sickling and destruction, the ...
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Sickle-cell anemia is a genetic disorder characterized by abnormal hemoglobin. One out of every 500 black children in the United States is affected by this disease. Eight to ten percent of the black population has the sickle-cell trait. While other hemoglobinopathies have been identified that also produce erythrocyte sickling and destruction, the ...
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Journal of the American Medical Association, 1950
The purpose of this report is to emphasize the possibility of the occasional early onset of sickle cell anemia and to consider it in the differential diagnosis of jaundice during the neonatal period in the Negro. Sickle cell anemia 1 is a hereditary and congenital disease of the hemopoietic system occurring almost entirely in members of the Negro race.
C A, FRAZIER, C E, RICE
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The purpose of this report is to emphasize the possibility of the occasional early onset of sickle cell anemia and to consider it in the differential diagnosis of jaundice during the neonatal period in the Negro. Sickle cell anemia 1 is a hereditary and congenital disease of the hemopoietic system occurring almost entirely in members of the Negro race.
C A, FRAZIER, C E, RICE
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Journal of Theoretical Biology, 1977
Abstract A number of metabolites have recently been investigated to determine whether or not they can prevent or reverse the sickling of red blood cells which contain the abnormal hemoglobin, hemoglobin S, of sickle cell anemia (SCA). An hypothesis is suggested in which one of these compounds, urea, may play a significant role in the precipitation of
Kirt J. Vener, Donald M. Perrill
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Abstract A number of metabolites have recently been investigated to determine whether or not they can prevent or reverse the sickling of red blood cells which contain the abnormal hemoglobin, hemoglobin S, of sickle cell anemia (SCA). An hypothesis is suggested in which one of these compounds, urea, may play a significant role in the precipitation of
Kirt J. Vener, Donald M. Perrill
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