Hemodynamic and functional assessment of patients with sickle cell disease and pulmonary hypertension.
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Group 5 Pulmonary Hypertension: The Orphan's Orphan Disease.The role of fibrocytes in sickle cell lung disease.Pulmonary complications of sickle cell disease.Proteomic identification of altered apolipoprotein patterns in pulmonary hypertension and vasculopathy of sickle cell diseasePulmonary hypertension in Nigerian adults with sickle cell anemia.Physical activity level and performance in the six-minute walk test of children and adolescents with sickle cell anemia.Segmentation and quantification of pulmonary artery for noninvasive CT assessment of sickle cell secondary pulmonary hypertension.Reconstructing sickle cell disease: a data-based analysis of the "hyperhemolysis paradigm" for pulmonary hypertension from the perspective of evidence-based medicine.Computed tomography correlates with cardiopulmonary hemodynamics in pulmonary hypertension in adults with sickle cell disease.Cellular, pharmacological, and biophysical evaluation of explanted lungs from a patient with sickle cell disease and severe pulmonary arterial hypertensionPulmonary function in children and adolescents with sickle cell disease: have we paid proper attention to this problem?Risk factors for death in 632 patients with sickle cell disease in the United States and United KingdomPulmonary hypertension in hemolytic disorders: pulmonary vascular disease: the global perspective.Exercise capacity and haemodynamics in patients with sickle cell disease with pulmonary hypertension treated with bosentan: results of the ASSET studies.Lung function and six-minute walk test performance in individuals with sickle cell disease.Elevated tricuspid regurgitation velocity and decline in exercise capacity over 22 months of follow up in children and adolescents with sickle cell anemia.Vasculopathy in sickle cell disease: Biology, pathophysiology, genetics, translational medicine, and new research directionsHematological 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 patientsVasculopathy and pulmonary hypertension in sickle cell disease.Sickle cell disease and venous thromboembolism: what the anticoagulation expert needs to knowUric Acid as a potential biomarker of pulmonary arterial hypertension in patients with sickle cell disease.Hospitalization for pain in patients with sickle cell disease treated with sildenafil for elevated TRV and low exercise capacity.Echocardiographic markers of elevated pulmonary pressure and left ventricular diastolic dysfunction are associated with exercise intolerance in adults and adolescents with homozygous sickle cell anemia in the United States and United Kingdom.Risk factors and mortality associated with an elevated tricuspid regurgitant jet velocity measured by Doppler-echocardiography in thalassemia: a Thalassemia Clinical Research Network reportAbnormalities in cardiac structure and function in adults with sickle cell disease are not associated with pulmonary hypertension.NT-pro brain natriuretic peptide levels and the risk of death in the cooperative study of sickle cell disease.Increased pulmonary pressures and myocardial wall stress in children with severe malariaReduced fitness and abnormal cardiopulmonary responses to maximal exercise testing in children and young adults with sickle cell anemia.Nitric oxide and arginine dysregulation: a novel pathway to pulmonary hypertension in hemolytic disordersA novel expression of exercise induced pulmonary hypertension in human immunodeficiency virus patients: a pilot study.Relative systemic hypertension in patients with sickle cell disease is associated with risk of pulmonary hypertension and renal insufficiencyA novel molecular signature for elevated tricuspid regurgitation velocity in sickle cell disease.Infrared imaging of nitric oxide-mediated blood flow in human sickle cell disease.Pathophysiology and treatment of pulmonary hypertension in sickle cell diseaseParadoxical protection from atherosclerosis and thrombosis in a mouse model of sickle cell disease.Allogeneic hematopoietic stem-cell transplantation for sickle cell disease.Reduced sensitivity of the ferroportin Q248H mutant to physiological concentrations of hepcidinClinical correlates of acute pulmonary events in children and adolescents with sickle cell diseaseHemodynamic predictors of mortality in adults with sickle cell disease
P2860
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P2860
Hemodynamic and functional assessment of patients with sickle cell disease and pulmonary hypertension.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
2007年學術文章
@zh
2007年學術文章
@zh-hant
name
Hemodynamic and functional ass ...... se and pulmonary hypertension.
@ast
Hemodynamic and functional ass ...... se and pulmonary hypertension.
@en
type
label
Hemodynamic and functional ass ...... se and pulmonary hypertension.
@ast
Hemodynamic and functional ass ...... se and pulmonary hypertension.
@en
prefLabel
Hemodynamic and functional ass ...... se and pulmonary hypertension.
@ast
Hemodynamic and functional ass ...... se and pulmonary hypertension.
@en
P2093
P2860
P921
P1476
Hemodynamic and functional ass ...... se and pulmonary hypertension.
@en
P2093
Anastasia Anthi
Angelo M Taveira-Dasilva
Christian J Hunter
Clara C Chen
James Nichols
Lewis J Rubin
Lori Hunter
Maria L Jison
Nilo A Avila
Roberto F Machado
P2860
P304
P356
10.1164/RCCM.200610-1498OC
P407
P577
2007-03-22T00:00:00Z