Results 181 to 190 of about 35,287 (246)
Comprehensive Review of Genetic and Epigenetic Regulation of Fetal Hemoglobin in β-Hemoglobinopathies: From Molecular Mechanisms to Clinical Applications. [PDF]
Mediterr J Hematol Infect DisAbu Za'ror YSM +7 more
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Serum Vitamin A levels in children with sickle cell anemia: relationship with pulmonary function indices. [PDF]
BMC PediatrEzenwosu OU +8 more
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First Antibiotic Prophylaxis Prescription Among Children With Sickle Cell Disease.
JAMA PediatrShi JS +6 more
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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 ...
openaire +2 more sources