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Significance of Systemic Scleroderma-Specific Autoantibodies in Idiopathic Interstitial Pneumonia. [PDF]
Murakami Y+5 more
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Evaluation of comorbidity burden on disease progression and mortality in patients with interstitial pneumonia with autoimmune features: A retrospective cohort study. [PDF]
Joerns EK+3 more
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Diagnosis of pulmonary sarcoidosis comorbid with non-specific interstitial pneumonia: a case report. [PDF]
Xu R, Wang K, Li W, Liu D.
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Lymphocytic Interstitial Pneumonia.
Clinics in Chest Medicine, 2016Lymphocytic interstitial pneumonia (LIP) is a rare lung disease on the spectrum of benign pulmonary lymphoproliferative disorders. LIP is frequently associated with connective tissue diseases or infections. Idiopathic LIP is rare; every attempt must be made to diagnose underlying conditions when LIP is diagnosed.
T. Panchabhai, C. Farver, K. Highland
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Long‐term clinical course and outcome of interstitial pneumonia with autoimmune features
Respirology (Carlton South. Print), 2020Idiopathic interstitial pneumonia (IIP) with autoimmune features that does not fulfil connective tissue disease (CTD) criteria has been recently defined as interstitial pneumonia with autoimmune features (IPAF). However, its long‐term clinical course and
H. Kim+4 more
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Nonspecific Interstitial Pneumonia
Seminars in Respiratory and Critical Care Medicine, 2020AbstractNonspecific interstitial pneumonia (NSIP) is a complex disorder commonly associated with other conditions such as connective tissue diseases (CTDs) and environmental exposures. Although idiopathic NSIP has been recognized as a separate clinical entity, recent studies have suggested that a proportion of these cases have autoimmune features ...
Alan K Y Teoh+3 more
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Nonspecific Interstitial Pneumonia
Seminars in Respiratory and Critical Care Medicine, 2006Nonspecific interstitial pneumonia (NSIP) describes a histopathologic pattern that can be seen in patients with immunodeficiency, drug or environmental exposures, and connective tissue diseases. The clinical diagnosis of NSIP, however, should be reserved for idiopathic cases in which no causative factor is identified.
Kevin R. Flaherty, Fernando J. Martinez
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