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.
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Negative health implications of sickle cell trait in high income countries: from the football field to the laboratoryEffects of hydration and dehydration on blood rheology in sickle cell trait carriers during exercisePatient-specific blood rheology in sickle-cell anaemia.Normal 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.Blood viscosity and the expression of inflammatory and adhesion markers in homozygous sickle cell disease subjects with chronic leg ulcers.Hematological and hemorheological determinants of the six-minute walk test performance in children with sickle cell anemia.The PhysioFlow thoracic impedancemeter is not valid for the measurements of cardiac hemodynamic parameters in chronic anemic patientsAcute moderate exercise does not further alter the autonomic nervous system activity in patients with sickle cell anemia.High red blood cell nitric oxide synthase activation is not associated with improved vascular function and red blood cell deformability in sickle cell anaemia.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 inflammationEffect of Age on Blood Rheology in Sickle Cell Anaemia and Sickle Cell Haemoglobin C Disease: A Cross-Sectional StudyHemorheological risk factors of acute chest syndrome and painful vaso-occlusive crisis in children with sickle cell disease.Low-shear red blood cell oxygen transport effectiveness is adversely affected by transfusion and further worsened by deoxygenation in sickle cell disease patients on chronic transfusion therapy.Prevalence of Sickle Cell Trait in the Southern Suburb of Beirut, LebanonHematologic 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.Severe proliferative retinopathy is associated with blood hyperviscosity in sickle cell hemoglobin-C disease but not in sickle cell anemiaPatients with sickle cell anemia on simple chronic transfusion protocol show sex differences for hemodynamic and hematologic responses to transfusion.Advances in understanding the pathogenesis of cerebrovascular vasculopathy in sickle cell anaemia.Diagnostic morphology: biophysical indicators for iron-driven inflammatory diseases.Clinical conditions responsible for hyperviscosity and skin ulcers complications.Sickle cell anemia in Brazil: personal, medical and endodontic patterns.Red blood cell nitric oxide synthase modulates red blood cell deformability in sickle cell anemia.Impaired blood rheology plays a role in the chronic disorders associated with sickle cell-hemoglobin C disease.Hydroxyurea treatment does not increase blood viscosity and improves red blood cell rheology in sickle cell anemia.Extracellular methemoglobin primes red blood cell aggregation in malaria: an in vitro mechanistic study.Quantification of Inter-Erythrocyte Forces with Ultra-High Frequency (410 MHz) Single Beam Acoustic Tweezer.Effects of oxidative stress on red blood cell rheology in sickle cell patients.In Vivo T1 of Blood Measurements in Children with Sickle Cell Disease Improve Cerebral Blood Flow Quantification from Arterial Spin-Labeling MRI.Impaired oxygen uptake efficiency slope and off-transient kinetics of pulmonary oxygen uptake in sickle cell anemia are associated with hemorheological abnormalities.Effects of hydration and water deprivation on blood viscosity during a soccer game in sickle cell trait carriers.Mild haemorheological changes induced by a moderate endurance exercise in patients with sickle cell anaemia.A proposed treatment algorithm for adults with Haemoglobin SC disease.Intraday blood rheological changes induced by Ramadan fasting in sickle cell trait carriers.Hemorheological alterations, decreased cerebral microvascular oxygenation and cerebral vasomotion compensation in sickle cell patients.Effects of hydroxyurea on blood rheology in sickle cell anemia: A two-years follow-up study.Exercise-induced changes in hematocrit and hematocrit/viscosity ratio in male rugby players.Influence of red blood cell aggregation on perfusion of an artificial microvascular network.
P2860
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P2860
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.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Red blood cell aggregation, ag ...... d sickle-hemoglobin C disease.
@en
type
label
Red blood cell aggregation, ag ...... d sickle-hemoglobin C disease.
@en
prefLabel
Red blood cell aggregation, ag ...... d sickle-hemoglobin C disease.
@en
P2093
P2860
P50
P1433
P1476
Red blood cell aggregation, ag ...... nd sickle-hemoglobin C disease
@en
P2093
Daniele Mougenel
Eric Beltan
Herbert J Meiselman
Julien Tripette
Olivier Hue
Roger Chout
Tamas Alexy
Tawfik Chalabi
P2860
P304
P356
10.3324/HAEMATOL.2008.005371
P577
2009-08-01T00:00:00Z