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Case Report: Innovative anesthetic approaches for whole lung lavage in an infant with pulmonary alveolar proteinosis. [PDF]
Front PediatrChen J +7 more
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Case report: Infantile pulmonary alveolar proteinosis associated with cytosolic isoleucyl-tRNA synthetase deficiency. [PDF]
Front PharmacolWu J +5 more
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Pulmonary alveolar proteinosis
Clinics in Chest Medicine, 2004Pulmonary alveolar proteinosis (PAP) has been recognized for almost half a century. At least three separate pathophysiologic mechanisms may lead to the characteristic feature of PAP: the excessive accumulation of surfactant lipoprotein in pulmonary alveoli, with associated disturbance of pulmonary gas exchange. The prognosis for adult patients with PAP
Presneill, JJ +3 more
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Pulmonary Alveolar Proteinosis
Radiology, 1969Since the original description of pulmonary alveolar proteinosis in 1958 (19), more than 100 cases have been reported. This article indicates the wide spectrum of roentgenographic changes (other than the well known batwing appearance) by reference to 5 patients in the San Francisco area who were examined recently.
J M, Davidson, W M, Macleod
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Pulmonary Alveolar Proteinosis
Respiration, 1974A case of alveolar proteinosis of the lungs with sarcoidal reaction of the lymph nodes is reported. The diagnosis was established by histological examination of lung tissue secured during thoracotomy.
J, Kurgan, K, Smigla
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PULMONARY ALVEOLAR PROTEINOSIS
Annals of Internal Medicine, 1960Excerpt Pulmonary alveolar proteinosis was first described by Rosen et al. in June, 1958.1We have had the opportunity to observe a patient with this disease, and wish to report the clinical, labora...
W R, EDMONDSON, J B, GERE
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Pulmonary Alveolar Proteinosis
Critical Reviews in Computed Tomography, 2003Case 1: A 52-year-old Caucasian retired police officer presented 3 years prior to diagnosis with the chief complaint of inability to exercise due to breathlessness. The patient was a long-distance walker who had given up this recreational activity due to dyspnea on exertion.
Bruce C, Trapnell +2 more
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Pulmonary Alveolar Proteinosis
New England Journal of Medicine, 1958WITHIN the past five years, and at an increasing rate within recent months, we have encountered 27 cases of a remarkable disease of the lung that consists of the filling of the alveoli by a PAS-positive proteinaceous material, rich in lipid. This material appears to be produced by the lining cells, which slough into the lumen, ultimately becoming ...
Samuel H. Rosen +4 more
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Autoimmune Pulmonary Alveolar Proteinosis
American Journal of Respiratory and Critical Care Medicine, 2022Autoimmune pulmonary alveolar proteinosis (PAP) is a rare disease characterized by myeloid cell dysfunction, abnormal pulmonary surfactant accumulation, and innate immune deficiency. It has a prevalence of 7-10 per million; occurs in individuals of all races, geographic regions, sex, and socioeconomic status; and accounts for 90% of all patients with ...
Cormac McCarthy +2 more
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Pulmonary Alveolar Proteinosis Syndrome
Seminars in Respiratory and Critical Care Medicine, 2020AbstractPulmonary alveolar proteinosis (PAP) is a syndrome characterized by progressive accumulation of pulmonary surfactant. This results in dyspnea, secondary pulmonary and systemic infection, and in some cases respiratory failure. PAP syndrome occurs in distinct diseases, classified according to pathogenetic mechanism; these include primary PAP (due
Alan, Kelly, Cormac, McCarthy
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