Use of Image Processing Techniques to Automatically Diagnose Sickle-Cell Anemia Present in Red Blood Cells Smear [PDF]
, 2013 Sickle Cell Anemia is a blood disorder which results from the abnormalities of red blood cells and shortens the life expectancy to 42 and 48 years for males and females respectively. It also causes pain, jaundice, shortness of breath, etc.
Barpanda, Siddharth Sekhar
core
Variation in the Amount of Hemoglobin S in a Patient with Sickle Cell Trait and Megaloblastic Anemia [PDF]
, 1963 Paul Heller +3 more
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Irreversibly sickled erythrocytes: a consequence of the heterogeneous distribution of hemoglobin types in sickle-cell anemia [PDF]
, 1968 John F. Bertles, Paul Milner
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Drugs for preventing red blood cell dehydration in people with sickle cell disease. [PDF]
, 2018 BACKGROUND: Sickle cell disease is an inherited disorder of hemoglobin, resulting in abnormal red blood cells. These are rigid and may block blood vessels leading to acute painful crises and other complications.
Ballas, Samir K., Nagalla, Srikanth
core +1 more source
The Effect of Amelioration of Anemia on the Synthesis of Fetal Hemoglobin in Sickle Cell Anemia [PDF]
, 1965 L Reed +2 more
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Red blood cell partitioning and segregation through vascular bifurcations in a model of sickle cell disease [PDF]
arXivThe impact of cell segregation and margination in blood disorders on microcirculatory hemodynamics within bifurcated vessels are physiologically significant, yet poorly understood. This study presents a comprehensive computational investigation of red blood cell (RBC) suspension dynamics, with a focus on a model of sickle cell disease (SCD) as an ...
arxiv
Augmentation of fetal hemoglobin (HbF) synthesis in culture by human erythropoietic precursors in the marrow and peripheral blood: studies in sickle cell anemia and nonhemoglobinopathic adults [PDF]
, 1978 K Kidoguchi +3 more
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Glucose 6-phosphate dehydrogenase deficiency and sickle cell anemia: frequency and features of the association in an African community [PDF]
, 1975 U Bienzle +3 more
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Quantitative studies of ferritinlike iron in erythrocytes of thalassemia, sickle-cell anemia, and hemoglobin Hammersmith with Mössbauer spectroscopy. [PDF]
, 1979 E. R. Bauminger +3 more
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Microcirculatory blood flow with aberrant levels of red blood cell aggregation [PDF]
arXivRecent clinical results indicate that aberrant erythrocyte aggregation in hematological disorders is accompanied by endothelial damage and glycocalyx disruption, but the underlying biophysical mechanisms remain unclear. This study uses direct computational modeling to explore how red blood cell (RBC) aggregation impacts shear stress in small blood ...
arxiv