Clinical correlates of steady-state oxyhaemoglobin desaturation in children who have sickle cell disease.
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Physiological correlates of intellectual function in children with sickle cell disease: hypoxaemia, hyperaemia and brain infarction.Magnetic resonance imaging in pediatric sickle cell anemia.Severe nocturnal and postexercise hypoxia in children and adolescents with sickle cell disease.Polysomnographic characteristics of a referred sample of children with sickle cell disease.Variability of pulse oximetry measurement over 1 year in children with sickle cell disease depends on initial oxygen saturation measurement.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 BelgiumClinical complications in pregnant women with sickle cell disease: prospective study of factors predicting maternal death or near missDeconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes.Periodic limb movements and disrupted sleep in children with sickle cell disease.Hydroxyurea Improves Oxygen Saturation in Children With Sickle Cell DiseaseGDP versus ESHAP Regimen in Relapsed and/or Refractory Hodgkin lymphoma: A Comparison Study.Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady StatePrognostic significance of early vaso-occlusive complications in children with sickle cell anemia.Laboratory and echocardiography markers in sickle cell patients with leg ulcersHemolysis in sickle cell mice causes pulmonary hypertension due to global impairment in nitric oxide bioavailabilityDaytime pulse oximeter measurements do not predict incidence of pain and acute chest syndrome episodes in sickle cell anemia.Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease.Non-invasive measurements of carboxyhemoglobin and methemoglobin in children with sickle cell disease.Cerebral tissue hemoglobin saturation in children with sickle cell disease.Hematological and Genetic Predictors of Daytime Hemoglobin Saturation in Tanzanian Children with and without Sickle Cell Anemia.The relationship between the severity of hemolysis, clinical manifestations and risk of death in 415 patients with sickle cell anemia in the US and EuropeDaytime steady-state haemoglobin desaturation is a risk factor for overt stroke in children with sickle cell anaemia.Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell diseaseElevated tricuspid regurgitant jet velocity in children and adolescents with sickle cell disease: association with hemolysis and hemoglobin oxygen desaturation.Haemoglobin oxygen saturation is a determinant of cerebral artery blood flow velocity in children with sickle cell anaemia.Prospective evaluation of haemoglobin oxygen saturation at rest and after exercise in paediatric sickle cell disease patients.An observational study of children with sickle cell disease in Kilifi, Kenya.Differences in the clinical and genotypic presentation of sickle cell disease around the world.Higher nocturnal and awake oxygen saturations in children with sickle cell disease receiving hydroxyurea therapy.Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in Tanzania.Prevalence of obstructive sleep apnea in children with sickle cell disease at a tertiary hospital in Saudi Arabia.Prevalence of obstructive sleep apnea in children and adolescents with sickle cell anemia.Sleep disordered breathing does not predict acute severe pain episodes in children with sickle cell anemia.Nocturnal hemoglobin desaturation is associated with reticulocytosis in adults with sickle cell disease and is independent of obstructive sleep apnea.Quality of sleep and pulmonary function in clinically stable adolescents with sickle cell anemia.Dense red blood cell and oxygen desaturation in sickle-cell disease.Transfusion-related adverse events are decreased in pregnant women with sickle cell disease by a change in policy from systematic transfusion to prophylactic oxygen therapy at home: A retrospective survey by the international sickle cell disease obs
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P2860
Clinical correlates of steady-state oxyhaemoglobin desaturation in children who have sickle cell disease.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Clinical correlates of steady- ...... who have sickle cell disease.
@ast
Clinical correlates of steady- ...... who have sickle cell disease.
@en
type
label
Clinical correlates of steady- ...... who have sickle cell disease.
@ast
Clinical correlates of steady- ...... who have sickle cell disease.
@en
prefLabel
Clinical correlates of steady- ...... who have sickle cell disease.
@ast
Clinical correlates of steady- ...... who have sickle cell disease.
@en
P2860
P1476
Clinical correlates of steady- ...... who have sickle cell disease.
@en
P2093
Charles T Quinn
Naveed Ahmad
P2860
P304
P356
10.1111/J.1365-2141.2005.05738.X
P407
P577
2005-10-01T00:00:00Z