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Pulmonary function abnormalities in young adults with thalassemia major

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dc.contributor.author Gourgoullanis, K en
dc.contributor.author Gouslou, A en
dc.contributor.author Papaioannou, G en
dc.contributor.author Halkias, C en
dc.contributor.author Stathakis, N en
dc.contributor.author Molyvdas, P en
dc.date.accessioned 2014-03-01T01:45:44Z
dc.date.available 2014-03-01T01:45:44Z
dc.date.issued 1997 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/24711
dc.subject Airway Obstruction en
dc.subject Carbon Monoxide en
dc.subject Electrocardiogram en
dc.subject Genetic Disorder en
dc.subject Growth Process en
dc.subject Heart Failure en
dc.subject Lung Disease en
dc.subject Lung Function en
dc.subject Lung Function Test en
dc.subject Lung Volume Measurements en
dc.subject Pulmonary Function en
dc.subject Respiratory Disease en
dc.subject Statistical Significance en
dc.subject Young Adult en
dc.subject Residual Volume en
dc.subject Serum Ferritin en
dc.subject Total Lung Capacity en
dc.subject Thalassemia Major en
dc.subject Vital Capacity en
dc.title Pulmonary function abnormalities in young adults with thalassemia major en
heal.type journalArticle en
heal.identifier.primary 10.1016/S0928-4680(97)00171-5 en
heal.identifier.secondary http://dx.doi.org/10.1016/S0928-4680(97)00171-5 en
heal.publicationDate 1997 en
heal.abstract Thalassemia seems to be the most common genetic disorder. The pathophysiologic mechanisms for lung impairment is not clear. Lung function tests in children showed small airway obstruction and restrictive lung changes. Forty-two patients, 22 females and 20 males, aged from 17 to 36 years old, with homozygous β-thalassemia were examined in a lung function laboratory. All patients received chelation therapy en
heal.journalName Pathophysiology en
dc.identifier.doi 10.1016/S0928-4680(97)00171-5 en


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