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Clinics in Chest Medicine, 1982
SUMMARY Idiopathic pulmonary fibrosis is a precise syndrome defined by clinical, roentgenographic, physiologic, and histopathologic features. Clinically, most patients have a nonproductive cough and dyspnea on exertion. The most common physical finding is the presence of crackles over the lower portions of both lungs; also, there may be clubbing ...
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SUMMARY Idiopathic pulmonary fibrosis is a precise syndrome defined by clinical, roentgenographic, physiologic, and histopathologic features. Clinically, most patients have a nonproductive cough and dyspnea on exertion. The most common physical finding is the presence of crackles over the lower portions of both lungs; also, there may be clubbing ...
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Human Pathology, 1970
Abstract The histopathologic changes in diffuse pulmonary fibrosis are discussed and current nomenclature reviewed. The importance of alveolitis due to hypersensitivity to inhaled organic proteins (allergic alveolitis) has been recognized only recently. The features that distinguish allergic alveolitis from other types of diffuse interstitial fibrosis
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Abstract The histopathologic changes in diffuse pulmonary fibrosis are discussed and current nomenclature reviewed. The importance of alveolitis due to hypersensitivity to inhaled organic proteins (allergic alveolitis) has been recognized only recently. The features that distinguish allergic alveolitis from other types of diffuse interstitial fibrosis
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Familial Idiopathic Pulmonary Fibrosis
2013Idiopathic pulmonary fibrosis (IPF) is a progressive interstitial lung disease of unknown etiology, with an appearance of usual interstitial pneumonia on lung biopsy. To-date, about a 100 families diagnosed with IPF have been described. Familial IPF is defined as histologically confirmed IPF occurring in two or more members of a family.
K, Wytrychowski +2 more
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Virchows Archiv A Pathological Anatomy and Histology, 1977
J C, Belton, N, Crise
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J C, Belton, N, Crise
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Der Internist, 2010
Many, different diseases can result in pulmonary fibrosis and its prevalence is continuously increasing. Pulmonary fibrosis is defined by a diffuse accumulation of connective tissue in the interstitial space resulting in destruction of lung parenchyma. Older individuals are more often affected by this disease than younger. Approximately one half of all
A, Prasse +2 more
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Many, different diseases can result in pulmonary fibrosis and its prevalence is continuously increasing. Pulmonary fibrosis is defined by a diffuse accumulation of connective tissue in the interstitial space resulting in destruction of lung parenchyma. Older individuals are more often affected by this disease than younger. Approximately one half of all
A, Prasse +2 more
openaire +1 more source
Pirfenidone in patients with idiopathic pulmonary fibrosis (CAPACITY): two randomised trials
Lancet, The, 2011Carlo Albera +2 more
exaly
Sildenafil for treatment of lung fibrosis and pulmonary hypertension: a randomised controlled trial
Lancet, The, 2002Ralph T Schermuly +2 more
exaly