Elevated tricuspid regurgitant jet velocity in children and adolescents with sickle cell disease: association with hemolysis and hemoglobin oxygen desaturation.
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Sickle cell disease: wheeze or asthma?Genetic determinants of haemolysis in sickle cell anaemia.The global burden of pulmonary hypertension in sickle cell disease: a systematic review and meta-analysis.Angiogenic and inflammatory markers of cardiopulmonary changes in children and adolescents with sickle cell disease.Spotlight on histamine dihydrochloride in acute myeloid leukaemia.Severe nocturnal and postexercise hypoxia in children and adolescents with sickle cell disease.Reconstructing sickle cell disease: a data-based analysis of the "hyperhemolysis paradigm" for pulmonary hypertension from the perspective of evidence-based medicine.Pulmonary 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 KingdomHigh levels of placenta growth factor in sickle cell disease promote pulmonary hypertensionLeft ventricular hypertrophy and diastolic dysfunction in children with sickle cell disease are related to asleep and waking oxygen desaturation.Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia.Levels of high-density lipoprotein cholesterol (HDL-C) among children with steady-state sickle cell disease.Acute chest syndrome: sickle cell disease.Reduction of the six-minute walk distance in children with sickle cell disease is correlated with silent infarct: results from a cross-sectional evaluation in a single center in BelgiumRisk factors for high cerebral blood flow velocity and death in Kenyan children with Sickle Cell Anaemia: role of haemoglobin oxygen saturation and febrile illnessElevated tricuspid regurgitation velocity and decline in exercise capacity over 22 months of follow up in children and adolescents with sickle cell anemia.Estimated pulmonary artery systolic pressure and sickle cell disease: a meta-analysis and systematic review.Doppler-defined pulmonary hypertension and the risk of death in children with sickle cell disease followed for a mean of three years.Vasculopathy in sickle cell disease: Biology, pathophysiology, genetics, translational medicine, and new research directionsVasculopathy and pulmonary hypertension in sickle cell disease.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 reportProspective echocardiography assessment of pulmonary hypertension and its potential etiologies in children with sickle cell disease.NT-pro brain natriuretic peptide levels and the risk of death in the cooperative study of sickle cell disease.Pleiotropic effects of intravascular haemolysis on vascular homeostasis.Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia.Pulmonary artery pressure and iron deficiency in patients with upregulation of hypoxia sensing due to homozygous VHL(R200W) mutation (Chuvash polycythemia).Pulmonary hypertension in lambs transfused with stored blood is prevented by breathing nitric oxideLow micromolar intravascular cell-free hemoglobin concentration affects vascular NO bioavailability in sickle cell disease: a computational analysisNon-invasive measurements of carboxyhemoglobin and methemoglobin in children with sickle cell disease.Genetic modifiers of sickle cell diseaseSickle cell anemia: iron availability and nocturnal oximetry.Impairment of neutrophil oxidative burst in children with sickle cell disease is associated with heme oxygenase-1.Abnormal pulmonary function and associated risk factors in children and adolescents with sickle cell anemia.Pathophysiology and treatment of pulmonary hypertension in sickle cell diseasePlasma thrombospondin-1 is increased during acute sickle cell vaso-occlusive events and associated with acute chest syndrome, hydroxyurea therapy, and lower hemolytic rates.The relationship between the severity of hemolysis, clinical manifestations and risk of death in 415 patients with sickle cell anemia in the US and EuropeClinical correlates of acute pulmonary events in children and adolescents with sickle cell diseaseHematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell disease
P2860
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P2860
Elevated tricuspid regurgitant jet velocity in children and adolescents with sickle cell disease: association with hemolysis and hemoglobin oxygen desaturation.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 11 February 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Elevated tricuspid regurgitant ...... emoglobin oxygen desaturation.
@en
Elevated tricuspid regurgitant ...... emoglobin oxygen desaturation.
@nl
type
label
Elevated tricuspid regurgitant ...... emoglobin oxygen desaturation.
@en
Elevated tricuspid regurgitant ...... emoglobin oxygen desaturation.
@nl
prefLabel
Elevated tricuspid regurgitant ...... emoglobin oxygen desaturation.
@en
Elevated tricuspid regurgitant ...... emoglobin oxygen desaturation.
@nl
P2093
P2860
P356
P1433
P1476
Elevated tricuspid regurgitant ...... emoglobin oxygen desaturation.
@en
P2093
Andrew Campbell
Caterina P Minniti
Craig Sable
Gregory Ensing
Mehdi Nouraie
Onyinye Onyekwere
Oswaldo L Castro
Sohail Rana
Victor R Gordeuk
P2860
P304
P356
10.3324/HAEMATOL.13812
P577
2009-02-11T00:00:00Z