Results 31 to 40 of about 247,564 (312)
BMC 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
Diagnosis of sickle cell anemia using AutoML on UV-Vis absorbance spectroscopy data [PDF]
arXiv, 2021 Sickle cell anemia is a genetic disorder that is widespread in many regions of the world. Early diagnosis through screening and preventive treatments are known to reduce mortality in the case of sickle cell disease (SCD). In addition, the screening of individuals with the largely asymptomatic condition of sickle cell trait (SCT) is necessary to curtail
arxiv
Arterial blood pressure in adult Nigerians with sickle cell anemia [PDF]
, 2010 SummaryAim and objectiveThis study was aimed at comparing the arterial blood pressures in steady state adult sickle cell patients with those of age- and sex-matched healthy controls.MethodsA descriptive cross-sectional study of 62 sickle cell anemia ...
Agwu, O. +6 more
core +1 more source
Sickle Cell Anemia and Its Phenotypes.
Annual review of genomics and human genetics (Print), 2018 In the 100 years since sickle cell anemia (SCA) was first described in the medical literature, studies of its molecular and pathophysiological basis have been at the vanguard of scientific discovery.
T. Williams, S. Thein
semanticscholar +1 more source
Predicting optimal hematocrit in silico [PDF]
Physical Review Fluids 3 (10), 103603 (2018), 2018 Optimal hematocrit $H_o$ maximizes oxygen transport. In healthy humans, the average hematocrit $H$ is in the range of 40-45$\%$, but it can significantly change in blood pathologies such as severe anemia (low $H$) and polycythemia (high $H$). Whether the hematocrit level in humans corresponds to the optimal one is a long standing physiological question.
arxiv +1 more source
Case 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
Journal of Information Systems and Informatics, 2023 In this study, we employed a Bayesian network approach for the classification of sickle cell anemia in teenagers based on their medical data. Sickle cell anemia is a hereditary blood disorder characterized by the presence of abnormal hemoglobin, leading ...
Blessing Ekong +4 more
doaj +1 more source
Large Language Models in Ambulatory Devices for Home Health Diagnostics: A case study of Sickle Cell Anemia Management [PDF]
arXiv, 2023 This study investigates the potential of an ambulatory device that incorporates Large Language Models (LLMs) in cadence with other specialized ML models to assess anemia severity in sickle cell patients in real time. The device would rely on sensor data that measures angiogenic material levels to assess anemia severity, providing real-time information ...
arxiv
Sickle Cell Anemia & Associated Neurological Complications: A Literature Review [PDF]
, 2022 Sickle cell anemia, an inherited disorder, causes red blood cells to contort into a disk or sickled shape becoming hard and sticky and obstructing blood flow.
Joseph, Rodjmar
core +1 more source
The kidney in sickle cell anemia
Kidney 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 ...
L. W. Statius Van Eps +4 more
openaire +3 more sources