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The Association of Serum Level of TGF-β<sub>1</sub> and Clinical Manifestations in Sickle Cell Anemia: A Case-Control Study. [PDF]
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Sickle cell anemia a molecular disease.
Science, 1949L. Pauling +3 more
semanticscholar +3 more sources
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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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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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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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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l-Glutamine for sickle cell anemia: more questions than answers.
Blood, 2018In 2017, the Food and Drug Administration approved 2 medications for sickle cell anemia (SCA): hydroxyurea for children and l-glutamine for children and adults.
C. Quinn
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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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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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A Comparative Analysis by KNN, SVM & ELM Classification to Detect Sickle Cell Anemia
2019 International Conference on Robotics,Electrical and Signal Processing Techniques (ICREST), 2019Red blood cell abnormalities involve erythrocytes that supply oxygen to all body tissues. Sometimes the formation and role of erythrocytes are hindered. Sickle cell anemia (SCA) is one kind of red blood cell disease.
Tajkia Saima Chy +1 more
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