Disease progression in idiopathic pulmonary fibrosis with mild physiological impairment: analysis from the Australian IPF registry
暂无分享,去创建一个
W. Cooper | P. Reynolds | I. Glaspole | S. Chapman | S. Ellis | N. Goh | P. Hopkins | S. Macansh | A. Mahar | Y. Moodley | C. Zappala | T. Corte | C. Grainge | G. Keir | E. Haydn Walters | H. Jo | Heather Allan | H. Walters | Sally Chapman | Samantha J Ellis | Wendy A. Cooper
[1] G. Gokçay,et al. The quality of sleep in nurses , 2017 .
[2] A. Hayen,et al. Baseline characteristics of idiopathic pulmonary fibrosis: analysis from the Australian Idiopathic Pulmonary Fibrosis Registry , 2017, European Respiratory Journal.
[3] H. Adamali,et al. A comparison of published multidimensional indices to predict outcome in idiopathic pulmonary fibrosis , 2017, ERJ Open Research.
[4] Wenbo Tang,et al. Nintedanib in patients with idiopathic pulmonary fibrosis and preserved lung volume , 2016, Thorax.
[5] S. Nathan,et al. Efficacy of pirfenidone in patients with idiopathic pulmonary fibrosis with more preserved lung function , 2016, European Respiratory Journal.
[6] R. D. du Bois,et al. Nintedanib in patients with idiopathic pulmonary fibrosis: Combined evidence from the TOMORROW and INPULSIS(®) trials. , 2016, Respiratory medicine.
[7] R. D. du Bois,et al. Pirfenidone for idiopathic pulmonary fibrosis: analysis of pooled data from three multinational phase 3 trials , 2016, European Respiratory Journal.
[8] R. Hubbard,et al. Global incidence and mortality of idiopathic pulmonary fibrosis: a systematic review , 2015, European Respiratory Journal.
[9] R. D. du Bois. 6-minute walk distance as a predictor of outcome in idiopathic pulmonary fibrosis , 2014, European Respiratory Journal.
[10] H. Collard,et al. Staging of idiopathic pulmonary fibrosis: past, present and future , 2014, European Respiratory Review.
[11] R. Sussman,et al. A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis. , 2014, The New England journal of medicine.
[12] Joyce S Lee,et al. A Multidimensional Index and Staging System for Idiopathic Pulmonary Fibrosis , 2012, Annals of Internal Medicine.
[13] F. Martinez,et al. Idiopathic pulmonary fibrosis: prognostic value of changes in physiology and six-minute-walk test. , 2006, American journal of respiratory and critical care medicine.
[14] F. D'Ovidio,et al. Six-minute-walk distance predicts waiting list survival in idiopathic pulmonary fibrosis. , 2006, American journal of respiratory and critical care medicine.
[15] G. Raghu,et al. The timed walk test as a measure of severity and survival in idiopathic pulmonary fibrosis , 2005, European Respiratory Journal.
[16] A. Nicholson,et al. Idiopathic pulmonary fibrosis: a composite physiologic index derived from disease extent observed by computed tomography. , 2003, American journal of respiratory and critical care medicine.
[17] J. Tooze,et al. Predicting survival in idiopathic pulmonary fibrosis: scoring system and survival model. , 2001, American journal of respiratory and critical care medicine.
[18] J. Egan,et al. Pulmonary function in idiopathic pulmonary fibrosis and referral for lung transplantation. , 2001, American journal of respiratory and critical care medicine.
[19] Efficacy and Safety of Nintedanib in Idiopathic Pulmonary Fibrosis. , 2015, The New England journal of medicine.
[20] A. Azuma,et al. A Phase 3 Trial of Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis , 2015 .
[21] Takeshi Johkoh,et al. American Thoracic Society Documents An Official ATS / ERS / JRS / ALAT Statement : Idiopathic Pulmonary Fibrosis : Evidence-based Guidelines for Diagnosis and Management , 2011 .
[22] S. Harari,et al. Walking distance on 6-MWT is a prognostic factor in idiopathic pulmonary fibrosis. , 2009, Respiratory medicine.
[23] T. Schaberg,et al. Lung function tests in patients with idiopathic pulmonary fibrosis. Are they helpful for predicting outcome? , 1997, Chest.