Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation
about
Negative health implications of sickle cell trait in high income countries: from the football field to the laboratoryMen with Sickle Cell Anemia and Priapism Exhibit Increased Hemolytic Rate, Decreased Red Blood Cell Deformability and Increased Red Blood Cell Aggregate StrengthRemote monitoring of pain and symptoms using wireless technology in children and adolescents with sickle cell diseaseNormal 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.Acute moderate exercise does not further alter the autonomic nervous system activity in patients with sickle cell anemia.Autonomic responses to cold face stimulation in sickle cell disease: a time-varying model analysis.Red blood cell deformability is reduced in homozygous sickle cell disease patients with leg ulcers.Effect 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.Guidelines on neonatal screening and painful vaso-occlusive crisis in sickle cell disease: Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular: Project guidelines: Associação Médica Brasileira - 2016.Relationships between systemic vascular resistance, blood rheology and nitric oxide in children with sickle cell anemia or sickle cell-hemoglobin C disease.Psychological aspects and hospitalization for pain crises in youth with sickle-cell disease.Plasma concentration of platelet-derived microparticles is related to painful vaso-occlusive phenotype severity in sickle cell anemia.Severe proliferative retinopathy is associated with blood hyperviscosity in sickle cell hemoglobin-C disease but not in sickle cell anemiaAdvances in understanding the pathogenesis of cerebrovascular vasculopathy in sickle cell anaemia.Coronary artery ectasia in atherosclerotic coronary artery disease, inflammatory disorders, and sickle cell disease.Clinical and Laboratory Predictors of Frequency of Painful Crises among Sickle Cell Anaemia Patients in Nigeria.A Prospective Comparison Study of Heart Rate Variability During Menses in Young Women With Dysmenorrhea.Conjunctival microvascular hemodynamics following vaso-occlusive crisis in sickle cell disease.Clinical conditions responsible for hyperviscosity and skin ulcers complications.Reticulocyte count is the most important predictor of acute cerebral ischemia and high-risk transcranial Doppler in a newborn cohort of 395 children with sickle cell anemia.Hydroxyurea treatment does not increase blood viscosity and improves red blood cell rheology in sickle cell anemia.Using the hemoglobin switch for the treatment of sickle cell disease.Individuals with sickle cell disease have a significantly greater vasoconstriction response to thermal pain than controls and have significant vasoconstriction in response to anticipation of pain.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.Effects of hydroxyurea on blood rheology in sickle cell anemia: A two-years follow-up study.Alpha-thalassaemia promotes frequent vaso-occlusive crises in children with sickle cell anaemia through haemorheological changes.Effects of Poloxamer 188 on red blood cell membrane properties in sickle cell anaemia.Rheology of red blood cells in patients with HbC disease.Haemolysis and abnormal haemorheology in sickle cell anaemia.Effect of inositol hexaphosphate-loaded red blood cells (RBCs) on the rheology of sickle RBCs.Changes in autonomic nervous activity during vaso-occlusive crisis in patients with sickle cell anaemia.CAREST--Multilingual Regional Integration for Health Promotion and Research on Sickle Cell Disease and Thalassemia.Pathophysiology and physical activity in patients with sickle cell anemia
P2860
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P2860
Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation
description
2011 nî lūn-bûn
@nan
2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Frequency of pain crises in si ...... ood viscosity and inflammation
@ast
Frequency of pain crises in si ...... ood viscosity and inflammation
@en
type
label
Frequency of pain crises in si ...... ood viscosity and inflammation
@ast
Frequency of pain crises in si ...... ood viscosity and inflammation
@en
prefLabel
Frequency of pain crises in si ...... ood viscosity and inflammation
@ast
Frequency of pain crises in si ...... ood viscosity and inflammation
@en
P2093
P2860
P50
P1433
P1476
Frequency of pain crises in si ...... ood viscosity and inflammation
@en
P2093
Andre Bowers
CAREST Study Group
Danitza Nebor
Harvey Reid
Jacques Elion
Jennifer Knight-Madden
Olivier Hue
Vanessa Cumming
P2860
P304
P356
10.3324/HAEMATOL.2011.047365
P577
2011-07-12T00:00:00Z