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A Health Educational Program for Mothers with Children Suffering from Sickle Cell Anemia [PDF]

open access: yesHelwan International Journal for Nursing Research and Practice
Background: Sickle cell anemia is a hereditary blood disorder characterized by the production of abnormal hemoglobin. Children with sickle cell anemia suffer from chronic pain, frequent infections, and fatigue due to the blockage of blood flow and the ...
Marwa Younes
doaj   +1 more source

Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell disease

open access: yesHaematologica, 2013
The aim of the study was to determine the factors associated with resting and exercise-induced hemoglobin oxygen desaturation. The well-established six-minute walk test was conducted in 107 sickle cell children (50 with sickle hemoglobin C disease and 57
Xavier Waltz   +12 more
doaj   +1 more source

Sickle Cell Anemia [PDF]

open access: yesJAMA: The Journal of the American Medical Association, 1922
Recent medical literature contains the records of three patients, all negroes, or negroes with an admixture of Caucasian blood, in whom severe anemia, characterized by certain peculiar morphologic alterations of the red blood cells, was present. The first case was reported by Herrick.1Washburn2published the records of a patient whose blood showed ...
openaire   +1 more source

Nutritional status, hospitalization and mortality among patients with sickle cell anemia in Tanzania

open access: yesHaematologica, 2011
Background Reduced growth is common in children with sickle cell anemia, but few data exist on associations with long-term clinical course. Our objective was to determine the prevalence of malnutrition at enrolment into a hospital-based cohort and ...
Sharon E. Cox   +8 more
doaj   +1 more source

Association between sickle cell and β-thalassemia genes and hemoglobin concentration and anemia in children and non-pregnant women in Sierra Leone: ancillary analysis of data from Sierra Leone’s 2013 National Micronutrient Survey

open access: yesBMC Research Notes, 2018
Objective By measuring the associations between the presence of sickle cell and β-thalassemia genes, we assessed the extent to which these hemoglobinopathies contribute to the high prevalence of anemia observed in preschool-aged children and women of ...
James P. Wirth   +4 more
doaj   +1 more source

Treating sickle cell anemia [PDF]

open access: yesScience, 2020
New drugs, stem cell transplants, and gene therapy show promise in treating sickle cell ...
John F, Tisdale   +2 more
openaire   +2 more sources

Prevalence of sickle cell disease and sickle cell trait in national neonatal screening studies

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2011
Sickle cell anemia is the best known hereditary blood disorder; there are serious complications associated with the condition. Diagnosis and early intervention reduce morbidity and mortality.
Luciana Garcia Lervolino   +5 more
doaj   +1 more source

Cardiac Arrhythmia in a Patient with Sickle Cell Anemia and Falciparum Malaria Treated with Intravenous Artesunate

open access: yesCase Reports in Infectious Diseases, 2019
Treatment of severe malaria with artemisinin derivatives in patients with comorbid conditions such as sickle cell anemia must be considered with precaution.
Abdulrahman Hummadi   +3 more
doaj   +1 more source

The kidney in sickle cell anemia

open access: yesKidney International, 1975
In 1910, Herrick described the first authentic case of sickle cell disease in a young student from Grenada in the West Indies [1]. He records that he was “uncertain whether the blood picture represented merely a freakish poikilocytosis or is dependent on some peculiar physical or chemical condition of the blood or is characteristic of some particular ...
Alleyne, George A.O.   +4 more
openaire   +2 more sources

Red blood cell aggregation, aggregate strength and oxygen transport potential of blood are abnormal in both homozygous sickle cell anemia and sickle-hemoglobin C disease

open access: yesHaematologica, 2009
Background Recent evidence suggests that red blood cell aggregation and the ratio of hematocrit to blood viscosity (HVR), an index of the oxygen transport potential of blood, might considerably modulate blood flow dynamics in the microcirculation.
Julien Tripette   +10 more
doaj   +1 more source

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