Histopathologic subsets of fibrosing alveolitis in patients with systemic sclerosis and their relationship to outcome.

By D. Bouros, A. Wells, A. Nicholson, T. Colby, V. Polychronopoulos, P. Pantelidis, P. Haslam, D. Vassilakis, C. Black, R. D. du Bois. American Journal of Respiratory and Critical Care Medicine, 2002

808 citations recorded by the source corpus.

Subfields: Pathology and Forensic Medicine, Pulmonary and Respiratory Medicine

View Paper: https://www.semanticscholar.org/paper/6671ac923e99c3c08be5850047e2d2577d3a12b8

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1. N. Hirani
2. A. Wells

Citations in the corpus

• Interstitial lung disease guideline (2008, background): “26 27 UIP may occur in connective tissue disease but the outcome, in contrast to IPF, is not uniformly poor.(28) 29 Thus, it is increasingly accepted that diagnosis of diffuse lung disease requires a multidisciplinary approach with the reconciliation of clinical, radiological and histological inform”
• A consensus document for the selection of lung transplant candidates: 2014--an update from the Pulmonary Transplantation Council of the International Society for Heart and Lung Transplantation. (2015, neutral): “33,34 If the lung disease has not responded to appropriate treatment and there are no extrapulmonary contraindications to transplantation, it is reasonable to use similar guidelines to those proposed for idiopathic ILD.”