Idiopathic pulmonary fibrosis and sleep disorders: no longer strangers in the night von Schiza, Sophia, Mermigkis, Charalampos, Margaritopoulos, George A, Daniil, Zoi, Harari, Sergio, Poletti, Venerino, Renzoni, Elizabetta A, Torre, Olga, Visca, Dina, Bouloukaki, Isolde, Sourvinos, George, Antoniou, Katerina M

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The impact of hiatus hernia in hypersensitivity pneumonitis von Heriot, David A, Stock, Carmel J W, Mumtaz, Zain-Ul-Abideen, Jenkins, R Gisli, Chua, Felix, Molyneaux, Phillip L, Devaraj, Anand, Kouranos, Vasilis, Wells, Athol U, Renzoni, Elizabetta A, Padley, Simon P G, Desai, Sujal R, George, Peter M

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Detection and Early Referral of Patients With Interstitial Lung Abnormalities: An Expert Survey Initiative von Hunninghake, Gary M, Goldin, Jonathan G, Kadoch, Michael A, Kropski, Jonathan A, Rosas, Ivan O, Wells, Athol U, Yadav, Ruchi, Lazarus, Howard M, Abtin, Fereidoun G, Corte, Tamera J, de Andrade, Joao A, Johannson, Kerri A, Kolb, Martin R, Lynch, David A, Oldham, Justin M, Spagnolo, Paolo, Strek, Mary E, Tomassetti, Sara, Washko, George R, White, Eric S

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Fibrotic Hypersensitivity Pneumonitis: Key Issues in Diagnosis and Management von Kouranos, Vasileios, Jacob, Joseph, Nicholson, Andrew, Renzoni, Elizabetta

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An integrated clinicoradiological staging system for pulmonary sarcoidosis: a case-cohort study von Walsh, Simon LF, Dr, Wells, Athol U, Prof, Sverzellati, Nicola, MD, Keir, Gregory J, MD, Calandriello, Lucio, MD, Antoniou, Katerina M, MD, Copley, Susan J, MD, Devaraj, Anand, MD, Maher, Toby M, PhD, Renzoni, Elizabetta, PhD, Nicholson, Andrew G, Prof, Hansell, David M, Prof

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Detection and Early Referral of Patients With Interstitial Lung Abnormalities von Hunninghake, Gary M., Goldin, Jonathan G., Kadoch, Michael A., Kropski, Jonathan A., Rosas, Ivan O., Wells, Athol U., Yadav, Ruchi, Lazarus, Howard M., Abtin, Fereidoun G., Corte, Tamera J., de Andrade, Joao A., Johannson, Kerri A., Kolb, Martin R., Lynch, David A., Oldham, Justin M., Spagnolo, Paolo, Strek, Mary E., Tomassetti, Sara, Washko, George R., White, Eric S., Abtin, Fereidoun, Antoniou, Katerina, Blackwell, Timothy, Brown, Kevin, Chung, Jonathan, Corte, Tamera, Crestani, Bruno, Crossno, Peter, Culver, Daniel, de Andrade, Joao, Deveraj, Anand, Flaherty, Kevin, Gudmundsson, Gunnar, Hatabu, Hiroto, Jacob, Joe, Johansson, Kerri, Kanne, Jeff, Kazerooni, Ella, Kolb, Martin, Lynch, David, Maher, Toby, Martinez, Fernando, Morais, Antonio, Nathan, Steven D., Noth, Imre, Oldham, Justin, Podolanczuk, Anna, Poletti, Venerino, Ravaglia, Claudia, Renzoni, Elizabetta, Richeldi, Luca, Rubin, Geoffrey, Ryerson, Chris, Sahoo, Debasis, Tomassetti, Sara, Spagnolo, Paolo, Strek, Mary E., Suh, Rob, Sverzellati, Nicola, Valeyre, Dominique, Walsh, Simon, Washko, George, White, Eric S.

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Patient eligibility for anti-fibrotic therapy in idiopathic pulmonary fibrosis can be altered by use of different sets of reference values for calculation of FVC percent predicted von Ward, Katie, Spurr, Lydia, Goldman, Nina R, Margaritopoulos, George A, Kokosi, Maria, Renzoni, Elizabetta, Chua, Felix, Maher, Toby M, Ward, Simon, Wells, Athol U

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Use of pulmonary arterial hypertension therapies in patient swith sarcoidosis-associated pulmonary hypertension von Price, Laura C, Kouranos, Vaileios, Baughman, Robert, Bloom, Chloe, Stewart, Iain, Shlobin, Oksana, Nathan, Steven, Dimopoulos, Konstantinos, Falconer, Jonathan, Gupta, Rohit, McCabe, Colm, Samaranayake, Chinthaka, Mason, Thomas, Mukherjee, Bhashkhar, Taube, Catherine, Sahni, Ankita, Kempny, Aleksander, Semple, Thomas, Renzoni, Elizabetta, Wells, Athol, Wort, S John

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