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Physiological responses of sickle cell trait carriers during exerciseDecreased hematocrit-to-viscosity ratio and increased lactate dehydrogenase level in patients with sickle cell anemia and recurrent leg ulcersNormal muscle oxygen consumption and fatigability in sickle cell patients despite reduced microvascular oxygenation and hemorheological abnormalities.Male gender, increased blood viscosity, body mass index and triglyceride levels are independently associated with systemic relative hypertension in sickle cell anemia.Hematological and hemorheological determinants of the six-minute walk test performance in children with sickle cell anemia.Acute moderate exercise does not further alter the autonomic nervous system activity in patients with sickle cell anemia.Blood thixotropy in patients with sickle cell anaemia: role of haematocrit and red blood cell rheological properties.Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammationHemorheological risk factors of acute chest syndrome and painful vaso-occlusive crisis in children with sickle cell disease.Differences of microparticle patterns between sickle cell anemia and hemoglobin SC patients.Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell diseaseRelationships between systemic vascular resistance, blood rheology and nitric oxide in children with sickle cell anemia or sickle cell-hemoglobin C disease.Blood rheology abnormalities and vascular cell adhesion mechanisms in sickle cell trait carriers during exercise.Plasma concentration of platelet-derived microparticles is related to painful vaso-occlusive phenotype severity in sickle cell anemia.Does increased red blood cell deformability raise the risk for osteonecrosis in sickle cell anemia?Central retinal vein occlusion in a sickle cell trait carrier after a cycling race.Relationship between acute chest syndrome and the sympatho-vagal balance in adults with hemoglobin SS disease; a case control study.Faster lactate transport across red blood cell membrane in sickle cell trait carriers.Endurance running trial in tropical environment: a blood rheological study.Impaired blood rheology plays a role in the chronic disorders associated with sickle cell-hemoglobin C disease.Effects of oxidative stress on red blood cell rheology in sickle cell patients.Impaired oxygen uptake efficiency slope and off-transient kinetics of pulmonary oxygen uptake in sickle cell anemia are associated with hemorheological abnormalities.Prevalence of sickle cell disease among Grenadian newborns.Physical activity level is not a determinant of autonomic nervous system activity and clinical severity in children/adolescents with sickle cell anemia: A pilot study.Hemorheological alterations, decreased cerebral microvascular oxygenation and cerebral vasomotion compensation in sickle cell patients.Pfaffia paniculata extract improves red blood cell deformability in sickle cell patients.Haemolysis and abnormal haemorheology in sickle cell anaemia.Alpha thalassemia protects sickle cell anemia patients from macro-albuminuria through its effects on red blood cell rheological properties.Is there a relationship between the hematocrit-to-viscosity ratio and microvascular oxygenation in brain and muscle?Natural antiband 3 antibodies in patients with sickle cell disease.Indirect viscosimetric method is less accurate than ektacytometry for the measurement of red blood cell deformability.Delayed beneficial effect of acute exercise on red blood cell aggregate strength in patients with sickle cell anemia.Effect of strenuous physical exercise on circulating cell-derived microparticles.Red blood cell deformability and aggregation, cell adhesion molecules, oxidative stress and nitric oxide markers after a short term, submaximal, exercise in sickle cell trait carriers.Sampling time after tourniquet removal affects erythrocyte deformability and aggregation measurements.Hemorheology and heart rate variability: is there a relationship?Does repeated and heavy exercise impair blood rheology in carriers of sickle cell trait?Effects of short supramaximal exercise on hemorheology in sickle cell trait carriers.Which side of the balance determines the frequency of vaso-occlusive crises in children with sickle cell anemia: Blood viscosity or microvascular dysfunction?Lipid profiles in French West Indies sickle cell disease cohorts, and their general population.
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Marie-Dominique Hardy-Dessources
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Marie-Dominique Hardy-Dessources
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Marie-Dominique Hardy-Dessources
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Marie-Dominique Hardy-Dessources
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Marie-Dominique Hardy-Dessources
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Marie-Dominique Hardy-Dessources
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Marie-Dominique Hardy-Dessources
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Marie-Dominique Hardy-Dessources
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Marie-Dominique Hardy-Dessources
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Marie-Dominique Hardy-Dessources
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Marie-Dominique Hardy-Dessources
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Marie-Dominique Hardy-Dessources
@nl