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Dendriform Pulmonary Ossification
(American Association of Respiratory Care, 2015)
Dendriform pulmonary ossification is a rare condition often diagnosed by either surgery or postmortem examination. We report a 43-y-old man with a history of nonproductive cough for 1 y. His physical examination was ...
Dendriform Pulmonary Ossification
(American Association of Respiratory Care, 2015)
Dendriform pulmonary ossification is a rare condition often diagnosed by either surgery or postmortem examination. We report a 43-y-old man with a history of nonproductive cough for 1 y. His physical examination was ...
Lung Diffusing Capacity Relates Better to Short-Term Progression on HRCT Abnormalities Than Spirometry in Mild Asbestosis
(WILEY-LISS, 2011)
Background Pulmonary function tests (PFT), particularly spirometry and lung diffusing capacity for carbon monoxide (DL(CO)), have been considered useful methods for the detection of the progression of interstitial asbestos ...
Biopsy-Proven Pulmonary Determinants of Heart Disease
(SPRINGER, 2010)
Heart disease (HD) can stress the alveolar blood-gas barrier, resulting in parenchymal inflammation and remodeling. Patients with HD may therefore display any of the symptoms commonly attributed to primary pulmonary disease, ...
Thin-section CT abnormalities and pulmonary gas exchange impairment in workers exposed to asbestos
(Radiological Soc North AmericaOak BrookEUA, 2004)
Comparative analysis of COPD associated with tobacco smoking, biomass smoke exposure or both
(BioMed Central Ltd., 2018)
Bilateral lung disease, extensive and diffuse. Diagnosis of pulmonary alveolar proteinosis by bronchoscopic cryobiopsy
(Elsevier, 2017)
Pulmonary alveolar proteinosis (PAP) is a rare disease characterized by the intra-alveolar accumulation of a
proteinaceous phospholipid-laden material called surfactant. Clinically, this disease should be suspected ...
Bilateral lung disease, extensive and diffuse. Diagnosis of pulmonary alveolar proteinosis by bronchoscopic cryobiopsy
(Elsevier, 2017)
Pulmonary alveolar proteinosis (PAP) is a rare disease characterized by the intra-alveolar accumulation of a
proteinaceous phospholipid-laden material called surfactant. Clinically, this disease should be suspected ...