-
1
-
-
79952717349
-
An Official ATS/ERS/JRS/ALAT Statement: Idiopathic pulmonary fibrosis: Evidence-based guidelines for diagnosis and management
-
Raghu G, Collard HR, Egan JJ, et al. An Official ATS/ERS/JRS/ALAT Statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med 2011; 183: 788-824.
-
(2011)
Am J Respir Crit Care Med
, vol.183
, pp. 788-824
-
-
Raghu, G.1
Collard, H.R.2
Egan, J.J.3
-
2
-
-
79956341531
-
Pirfenidone in patients with idiopathic pulmonary fibrosis (CAPACITY): Two randomised trials
-
Noble PW, Albera C, Bradford WZ, et al. Pirfenidone in patients with idiopathic pulmonary fibrosis (CAPACITY): two randomised trials. Lancet 2011; 377: 1760-9.
-
(2011)
Lancet
, vol.377
, pp. 1760-1769
-
-
Noble, P.W.1
Albera, C.2
Bradford, W.Z.3
-
3
-
-
84901759236
-
A Phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis
-
King TE Jr, Bradford WZ, Castro-Bernardini S, et al. A Phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis. N Engl J Med 2014; 370: 2083-92.
-
(2014)
N Engl J Med
, vol.370
, pp. 2083-2092
-
-
King, T.E.1
Bradford, W.Z.2
Castro-Bernardini, S.3
-
4
-
-
84901810710
-
Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis
-
Richeldi L, du Bois RM, Raghu G, et al. Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis. N Engl J Med 2014; 370: 2071-82.
-
(2014)
N Engl J Med
, vol.370
, pp. 2071-2082
-
-
Richeldi, L.1
Du Bois, R.M.2
Raghu, G.3
-
5
-
-
84455168726
-
Forced vital capacity in patients with idiopathic pulmonary fibrosis: Test properties and minimal clinically important difference
-
du Bois RM, Weycker D, Albera C, et al. Forced vital capacity in patients with idiopathic pulmonary fibrosis: test properties and minimal clinically important difference. Am J Respir Crit Care Med 2011; 184: 1382-9.
-
(2011)
Am J Respir Crit Care Med
, vol.184
, pp. 1382-1389
-
-
Du Bois, R.M.1
Weycker, D.2
Albera, C.3
-
6
-
-
0041874992
-
Changes in clinical and physiologic variables predict survival in idiopathic pulmonary fibrosis
-
Collard HR, King TE Jr, Bartelson BB, et al. Changes in clinical and physiologic variables predict survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2003; 168: 538-42.
-
(2003)
Am J Respir Crit Care Med
, vol.168
, pp. 538-542
-
-
Collard, H.R.1
King, T.E.2
Bartelson, B.B.3
-
7
-
-
0041374153
-
Prognostic implications of physiologic and radiographic changes in idiopathic interstitial pneumonia
-
Flaherty KR, Mumford JA, Murray S, et al. Prognostic implications of physiologic and radiographic changes in idiopathic interstitial pneumonia. Am J Respir Crit Care Med 2003; 168: 543-8.
-
(2003)
Am J Respir Crit Care Med
, vol.168
, pp. 543-548
-
-
Flaherty, K.R.1
Mumford, J.A.2
Murray, S.3
-
8
-
-
20144381640
-
Physiology is a stronger predictor of survival than pathology in fibrotic interstitial pneumonia
-
Jegal Y, Kim DS, Shim TS, et al. Physiology is a stronger predictor of survival than pathology in fibrotic interstitial pneumonia. Am J Respir Crit Care Med 2005; 171: 639-44.
-
(2005)
Am J Respir Crit Care Med
, vol.171
, pp. 639-644
-
-
Jegal, Y.1
Kim, D.S.2
Shim, T.S.3
-
9
-
-
77951170794
-
Marginal decline in forced vital capacity is associated with a poor outcome in idiopathic pulmonary fibrosis
-
Zappala CJ, Latsi PI, Nicholson AG, et al. Marginal decline in forced vital capacity is associated with a poor outcome in idiopathic pulmonary fibrosis. Eur Respir J 2010; 35: 830-6.
-
(2010)
Eur Respir J
, vol.35
, pp. 830-836
-
-
Zappala, C.J.1
Latsi, P.I.2
Nicholson, A.G.3
-
10
-
-
80051819865
-
Ascertainment of individual risk of mortality in patients with idiopathic pulmonary fibrosis
-
du Bois RM, Weycker D, Albera C, et al. Ascertainment of individual risk of mortality in patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2011; 184: 459-66.
-
(2011)
Am J Respir Crit Care Med
, vol.184
, pp. 459-466
-
-
Du Bois, R.M.1
Weycker, D.2
Albera, C.3
-
11
-
-
84862826491
-
Relative versus absolute change in forced vital capacity in idiopathic pulmonary fibrosis
-
Richeldi L, Ryerson CJ, Lee JS, et al. Relative versus absolute change in forced vital capacity in idiopathic pulmonary fibrosis. Thorax 2012; 67: 407-11.
-
(2012)
Thorax
, vol.67
, pp. 407-411
-
-
Richeldi, L.1
Ryerson, C.J.2
Lee, J.S.3
-
12
-
-
20544443765
-
The clinical course of patients with idiopathic pulmonary fibrosis
-
Martinez FJ, Safrin S, Weycker D, et al. The clinical course of patients with idiopathic pulmonary fibrosis. Ann Intern Med 2005; 142: 963-7.
-
(2005)
Ann Intern Med
, vol.142
, pp. 963-967
-
-
Martinez, F.J.1
Safrin, S.2
Weycker, D.3
-
14
-
-
84896767563
-
Predicting pulmonary fibrosis disease course from past trends in pulmonary function
-
Schmidt SL, Tayob N, Han MK, et al. Predicting pulmonary fibrosis disease course from past trends in pulmonary function. Chest 2014; 145: 579-85.
-
(2014)
Chest
, vol.145
, pp. 579-585
-
-
Schmidt, S.L.1
Tayob, N.2
Han, M.K.3
-
15
-
-
84918842765
-
Combination therapy: The future of management for idiopathic pulmonary fibrosis?
-
Wuyts WA, Antoniou KM, Borensztajn K, et al. Combination therapy: the future of management for idiopathic pulmonary fibrosis? Lancet Respir Med 2014; 2: 933-42.
-
(2014)
Lancet Respir Med
, vol.2
, pp. 933-942
-
-
Wuyts, W.A.1
Antoniou, K.M.2
Borensztajn, K.3
-
16
-
-
84878454263
-
Idiopathic pulmonary fibrosis: Current challenges and future perspectives
-
Richeldi L. Idiopathic pulmonary fibrosis: current challenges and future perspectives. Eur Respir Rev 2013; 22: 103-5.
-
(2013)
Eur Respir Rev
, vol.22
, pp. 103-105
-
-
Richeldi, L.1
-
17
-
-
84865112235
-
Idiopathic pulmonary fibrosis: Lung function is a clinically meaningful endpoint for phase III trials
-
du Bois RM, Nathan SD, Richeldi L, et al. Idiopathic pulmonary fibrosis: lung function is a clinically meaningful endpoint for phase III trials. Am J Respir Crit Care Med 2012; 186: 712-15.
-
(2012)
Am J Respir Crit Care Med
, vol.186
, pp. 712-715
-
-
Du Bois, R.M.1
Nathan, S.D.2
Richeldi, L.3
|