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Journal of Human Nutrition and Dietetics, Volume 39, Issue 4, August 2026.This novel qualitative study provides primary data that reflects the sickle cell service user/carer voice about the changes needed to redefine and integrate nutritional management in standard SCD care. ABSTRACT Introduction Nutrition is not currently integrated into standard care provision in sickle cell disease (SCD) impacting patients experience ...
Claudine Matthews +3 more
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Transfusion, Volume 66, Issue 8, Page 1613-1623, August 2026.Abstract Background Standardized post‐graduate education in pediatric transfusion medicine remains limited. The objective of this study was to adapt an adult transfusion education program, Transfusion Camp, to include pediatric content and assess knowledge improvement in pediatric subspecialty trainees.
Ines Zuna +14 more
wiley +1 more source
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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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THE ADOLESCENT WITH SICKLE CELL ANEMIA
Hematology/Oncology Clinics of North America, 1996Adolescence is a time of intense change and turmoil. Helping patients with sickle cell disease have a smooth transition from the pediatric to adult health care environment is an important and meaningful experience. Facilitating the patient's transition, however, takes time and effort.
T R, Kinney, R E, Ware
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The electrocardiogram in sickle-cell anemia
American Heart Journal, 1955Abstract 1. 1. Sixty random patients with a hematologic diagnosis of sickle-cell anemia have been studied for clinical and electrocardiographic evidence of heart disease. 2. 2. The various types of electrocardiographic abnormalities have been discussed and compared with those found in the literature.
C L, LINDO, L R, DOCTOR
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Hypersplenism in Sickle Cell Anemia
Archives of Internal Medicine, 1964Although splenomegaly in children with sickle cell anemia is common, massive enlargement associated with thrombocytopenia and very severe anemia is rare. In such patients, splenectomy has been followed by increase in platelet count and hemoglobin concentration. This suggests that an acquired hypersplenism aggravated the hemolytic process.
E C, ROSSI +3 more
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Cholestasis in sickle cell anemia
The American Journal of Medicine, 1964Abstract A patient with sickle cell anemia who presented with marked cholestatic jaundice is described, with emphasis upon the difficulties encountered in differentiating this symptom complex from extrahepatic obstruction due to stone formation. This patient had extraordinarily high serum bilirubin levels, apparently the result of increased bilirubin ...
F M, KLION, M J, WEINER, F, SCHAFFNER
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PATHOPHYSIOLOGY OF SICKLE CELL ANEMIA
Hematology/Oncology Clinics of North America, 1996The anemia results from the markedly shortened circulatory survival of SS cells, together with a limited erythropoietic response. Both independent properties of Hb S-polymerization of the deoxy-Hb and instability of the oxy-Hb-contribute to early red cell destruction by effects on the Hb and on the red cell membranes.
R M, Bookchin, V L, Lew
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