Prospective evaluation of haemoglobin oxygen saturation at rest and after exercise in paediatric sickle cell disease patients. - Wikidata - awgldk - TriplyDB

Prospective evaluation of haemoglobin oxygen saturation at rest and after exercise in paediatric sickle cell disease patients.

Prospective evaluation of haemoglobin oxygen saturation at rest and after exercise in paediatric sickle cell disease patients.

http://www.wikidata.org/entity/Q37404519

about

Severe nocturnal and postexercise hypoxia in children and adolescents with sickle cell disease.Physical activity level and performance in the six-minute walk test of children and adolescents with sickle cell anemia.Pulmonary function in children and adolescents with sickle cell disease: have we paid proper attention to this problem?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 Belgium Elevated tricuspid regurgitation velocity and decline in exercise capacity over 22 months of follow up in children and adolescents with sickle cell anemia.Laboratory and echocardiography markers in sickle cell patients with leg ulcers Anemia, age, desaturation, and impaired neurocognition in sickle cell anemia.Sickle cell disease is associated with decreased HIV but higher HBV and HCV comorbidities in U.S. hospital discharge records: a cross-sectional study.Sickle cell anemia: iron availability and nocturnal oximetry.Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell disease Sleep-disordered breathing and nocturnal hypoxemia in young adults with sickle cell disease.Pulmonary hypertension in children with sickle cell disease.Proteinuria is associated with elevated tricuspid regurgitant jet velocity in children with sickle cell disease.Advances in understanding the pathogenesis of cerebrovascular vasculopathy in sickle cell anaemia.Fetal Hemoglobin is Associated with Peripheral Oxygen Saturation in Sickle Cell Disease in Tanzania.The 6-min walk test: an independent correlate of elevated tricuspid regurgitant jet velocity in children and young adult sickle cell patients.Tricuspid regurgitant jet velocity and hospitalization in Tanzanian children with sickle cell anemia How can anemia negatively influence gas exchange?Dense red blood cell and oxygen desaturation in sickle-cell disease.Pathophysiology and physical activity in patients with sickle cell anemia Prevention of Morbidity in sickle cell disease--qualitative outcomes, pain and quality of life in a randomised cross-over pilot trial of overnight supplementary oxygen and auto-adjusting continuous positive airways pressure (POMS2a): study protocol f A ten year review of the sickle cell program in Muhimbili National Hospital, Tanzania

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Prospective evaluation of haemoglobin oxygen saturation at rest and after exercise in paediatric sickle cell disease patients.

http://www.wikidata.org/entity/Q37404519

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 19 August 2009

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vedecký článok

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vetenskaplig artikel

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Prospective evaluation of haem ...... sickle cell disease patients.

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Prospective evaluation of haem ...... sickle cell disease patients.

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Prospective evaluation of haem ...... sickle cell disease patients.

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Prospective evaluation of haem ...... sickle cell disease patients.

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J.1365-2141.2009.07854.X

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British Journal of Haematology

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Prospective evaluation of haem ...... sickle cell disease patients.

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Andrew Campbell

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Caterina P Minniti

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Craig Sable

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Gregory Ensing

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Lori Luchtman-Jones

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Manuel Arteta

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Mehdi Nouraie

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Niti Dham

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Onyinye Onyekwere

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Oswaldo L Castro

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P2860

Spirometric reference values from a sample of the general U.S. population

Standardisation of the measurement of lung volumes

Standardisation of the single-breath determination of carbon monoxide uptake in the lung

Interpretative strategies for lung function tests

Standardisation of spirometry

ATS statement: guidelines for the six-minute walk test.

Erythrocyte Hb-S concentration. An important factor in the low oxygen affinity of blood in sickle cell anemia.

Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes.

Clinical correlates of steady-state oxyhaemoglobin desaturation in children who have sickle cell disease.

Daytime pulse oximeter measurements do not predict incidence of pain and acute chest syndrome episodes in sickle cell anemia.

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352-359

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10.1111/J.1365-2141.2009.07854.X

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Gregory J. Kato

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26755255

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19694721

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