Intravascular hemolysis and the pathophysiology of sickle cell disease

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Items 301–400 of 746

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4. Effect of hydroxyurea therapy on intravascular hemolysis and endothelial dysfunction markers in sickle cell anemia patients
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15. Alpha thalassemia, but not βS-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort
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18. Protein aggregation-inhibition: a therapeutic route from Parkinson’s disease to sickle cell anemia
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19. Relationship between ventilation heterogeneity and exercise intolerance in adults with sickle cell anemia
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28. Cardiac diastolic maladaptation is associated with the severity of exercise intolerance in sickle cell anemia patients
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29. Vasculopathy in Sickle Cell Disease: From Red Blood Cell Sickling to Vascular Dysfunction
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30. Accelerated approval of Oxbryta® (voxelotor): A case study on novel endpoint selection in sickle cell disease
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31. Oxidative stress and hepcidin expression in pediatric sickle cell anemia with iron overload
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32. Improving packed red blood cell storage with a high-viscosity buffered storage solution
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33. Circulating Small Extracellular Vesicles May Contribute to Vaso-Occlusive Crises in Sickle Cell Disease
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34. Functional foods: promising therapeutics for Nigerian Children with sickle cell diseases
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35. Antithrombin‐III mitigates thrombin‐mediated endothelial cell contraction and sickle red blood cell adhesion in microscale flow
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36. Cardiovascular consequences of sickle cell disease
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37. Clinical and laboratory characterization of adult sickle cell anemia patients in Kinshasa
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38. Sickle cell vasculopathy: vascular phenotype on fire!
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39. Priapism in patients with hemolytic disorders: a nationwide retrospective cohort study
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40. Genetic contribution and functional impairment of inflammasome in sickle cell disease
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41. Does Pathological Iron Overload Impair the Function of Human Lungs?
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42. Fetal-like Hemoglobin in Sickle Cell Anemia
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43. Scavenger receptor CD163 multimerises to allow uptake of diverse ligands
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45. Monitoring retinal pathology and cerebral injury in sickle cell disease using spectral‐domain optical coherence tomography in pediatric patients
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46. Role of ribosomal RNA released from red cells in blood coagulation in zebrafish and humans
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48. Long-Term Effects of Allogeneic Hematopoietic Stem Cell Transplantation on Systemic Inflammation in Sickle Cell Disease Patients
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49. Sex-specific genetic modifiers identified susceptibility of cold stored red blood cells to osmotic hemolysis
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51. Plasma levels of E‐selectin are associated with retinopathy in sickle cell disease
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52. Metabolic correlates to critical speed in murine models of sickle cell disease
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54. Posttranslational modifications of sickle hemoglobin in microparticles may promote injury
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56. Precision Medicine for Pulmonary Vascular Disease: The Future Is Now (2023 Grover Conference Series)
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58. Sickle Cell Diastolic Cardiomyopathy and Mortality Risk: A Novel Echocardiographic Framework for Prognostic Stratification
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59. Associations of hemolysis and anemia with cardiopulmonary dysfunction in an adult sickle cell disease cohort
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