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Diseases of the Chest, 1951
1)The term Familial Pulmonary Fibrosis is felt to be a definite entity. 2)This disease is a familial response to chronic pulmonary insult in the nature of bilateral pulmonary fibrosis. 3)The disease, once it manifests itself clinically, is usually progressive to death. 4)The age incidence is from 30 to 55 years.
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1)The term Familial Pulmonary Fibrosis is felt to be a definite entity. 2)This disease is a familial response to chronic pulmonary insult in the nature of bilateral pulmonary fibrosis. 3)The disease, once it manifests itself clinically, is usually progressive to death. 4)The age incidence is from 30 to 55 years.
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[Idiopathic pulmonary fibrosis].
Presse medicale (Paris, France : 1983), 2006Idiopathic pulmonary fibrosis is a chronic disorder characterized histopathologically by a pattern of usual interstitial pneumonia, with heterogeneous and mutilating interstitial fibrosis with foci of proliferating fibroblasts, honeycomb lung, and little if any inflammation.
Cottin, Vincent, Cordier, Jean-François
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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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Immune-checkpoint inhibitors: long-term implications of toxicity
Nature Reviews Clinical Oncology, 2022Douglas B Johnson, Msci +2 more
exaly
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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