-
1
-
-
84861394764
-
Prednisolone, azathioprine and N-acetylcysteine for pulmonary fibrosis
-
Idiopathic Pulmonary Fibrosis Clinical Research Network
-
Raghu G, Anstrom KJ, King TE Jr, et al. Idiopathic Pulmonary Fibrosis Clinical Research Network. Prednisolone, azathioprine and N-acetylcysteine for pulmonary fibrosis. N Engl J Med 2012;366: 1968-77.
-
(2012)
N Engl J Med
, vol.366
, pp. 1968-1977
-
-
Raghu, G.1
Anstrom, K.J.2
King Jr., T.E.3
-
2
-
-
0041374155
-
Fibrotic idiopathic interstitial pneumonia: The prognostic value of longitudinal functional trends
-
DOI 10.1164/rccm.200210-1245OC
-
Latsi PI, du Bois RM, Nicholson AG, et al. Fibrotic idiopathic interstitial pneumonia: the prognostic value of longitudinal functional trends. Am J Respir Crit Care Med 2003;168:531-7. (Pubitemid 37088594)
-
(2003)
American Journal of Respiratory and Critical Care Medicine
, vol.168
, Issue.5
, pp. 531-537
-
-
Latsi, P.I.1
Du Bois, R.M.2
Nicholson, A.G.3
Colby, T.V.4
Bisirtzoglou, D.5
Nikolakopoulou, A.6
Veeraraghavan, S.7
Hansell, D.M.8
Wells, A.U.9
-
3
-
-
0041874992
-
Changes in clinical and physiologic variables predict survival in idiopathic pulmonary fibrosis
-
DOI 10.1164/rccm.200211-1311OC
-
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. (Pubitemid 37088595)
-
(2003)
American Journal of Respiratory and Critical Care Medicine
, vol.168
, Issue.5
, pp. 538-542
-
-
Collard, H.R.1
King Jr., T.E.2
Bartelson, B.B.3
Vourlekis, J.S.4
Schwarz, M.I.5
Brown, K.K.6
-
4
-
-
0041374153
-
Prognostic implications of physiologic and radiographic changes in idiopathic interstitial pneumonia
-
DOI 10.1164/rccm.200209-1112OC
-
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. (Pubitemid 37088596)
-
(2003)
American Journal of Respiratory and Critical Care Medicine
, vol.168
, Issue.5
, pp. 543-548
-
-
Flaherty, K.R.1
Mumford, J.A.2
Murray, S.3
Kazerooni, E.A.4
Gross, B.H.5
Colby, T.V.6
Travis, W.D.7
Flint, A.8
Toews, G.B.9
Lynch III, J.P.10
Martinez, F.J.11
-
5
-
-
13844316832
-
Analyses of efficacy end points in a controlled trial of interferon-γ1b for idiopathic pulmonary fibrosis
-
DOI 10.1378/chest.127.1.171
-
King TE Jr, Safrin S, Starko KM, et al. Analyses of efficacy end points in a controlled trial of interferon-gamma1b for idiopathic pulmonary fibrosis. Chest 2005;127:171-7. (Pubitemid 41724573)
-
(2005)
Chest
, vol.127
, Issue.1
, pp. 171-177
-
-
King Jr., T.E.1
Safrin, S.2
Starko, K.M.3
Brown, K.K.4
Noble, P.W.5
Raghu, G.6
Schwartz, D.A.7
-
6
-
-
20144381640
-
Physiology is a stronger predictor of survival than pathology in fibrotic interstitial pneumonia
-
DOI 10.1164/rccm.200403-331OC
-
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. (Pubitemid 40365421)
-
(2005)
American Journal of Respiratory and Critical Care Medicine
, vol.171
, Issue.6
, pp. 639-644
-
-
Jegal, Y.1
Dong, S.K.2
Tae, S.S.3
Lim, C.-M.4
Sang, D.L.5
Koh, Y.6
Woo, S.K.7
Won, D.K.8
Jin, S.L.9
Travis, W.D.10
Kitaichi, M.11
Colby, T.V.12
-
7
-
-
78349278073
-
Fibrotic idiopathic interstitial pneumonias: Mortality is linked to a decline in gas transfer
-
Peelen L, Wells AU, Prijs M, et al. Fibrotic idiopathic interstitial pneumonias: mortality is linked to a decline in gas transfer. Respirology 2010;15:1233-43.
-
(2010)
Respirology
, vol.15
, pp. 1233-1243
-
-
Peelen, L.1
Wells, A.U.2
Prijs, M.3
-
8
-
-
84859918517
-
Pulmonary function vascular index predicts prognosis in idiopathic interstitial pneumonia
-
Corte TJ, Wort SJ, Macdonald PS, et al. Pulmonary function vascular index predicts prognosis in idiopathic interstitial pneumonia. Respirology 2012;17:674-80.
-
(2012)
Respirology
, vol.17
, pp. 674-680
-
-
Corte, T.J.1
Wort, S.J.2
Macdonald, P.S.3
-
9
-
-
79960193484
-
Pulmonary function measures predict mortality differently in idiopathic pulmonary fibrosis versus combined pulmonary fibrosis and emphysema
-
Schmidt SL, Nambiar AM, Tayob N, et al. Pulmonary function measures predict mortality differently in idiopathic pulmonary fibrosis versus combined pulmonary fibrosis and emphysema. Eur Respir J 2011;38:176-83.
-
(2011)
Eur Respir J
, vol.38
, pp. 176-183
-
-
Schmidt, S.L.1
Nambiar, A.M.2
Tayob, N.3
-
10
-
-
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
-
11
-
-
80051819865
-
Ascertainment of individual risk of mortality for patients with idiopathic pulmonary fibrosis
-
du Bois RM, Weycker D, Albera C, et al. Ascertainment of individual risk of mortality for 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
-
12
-
-
84861382039
-
Idiopathic pulmonary fibrosis: Clinically meaningful primary end-points in phase 3 clinical trials
-
Raghu G, Collard HR, Anstrom KJ, et al. Idiopathic pulmonary fibrosis: clinically meaningful primary end-points in phase 3 clinical trials. Am J Respir Crit Care Med 2012;185:1044-8.
-
(2012)
Am J Respir Crit Care Med
, vol.185
, pp. 1044-1048
-
-
Raghu, G.1
Collard, H.R.2
Anstrom, K.J.3
-
13
-
-
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
-
14
-
-
0034011982
-
Idiopathic pulmonary fibrosis: Diagnosis and treatment. International consensus statement
-
American Thoracic Society
-
American Thoracic Society. Idiopathic pulmonary fibrosis: diagnosis and treatment. International consensus statement. Am J Respir Crit Care Med 2000;161:646-64.
-
(2000)
Am J Respir Crit Care Med
, vol.161
, pp. 646-664
-
-
-
15
-
-
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
-
16
-
-
0031000724
-
Lone cryptogenic fibrosing alveolitis: A functional-morphologic correlation based on extent of disease on thin-section computed tomography
-
Wells AU, King AD, Rubens MB, et al. Lone CFA: a functional-morphological correlation based on extent of disease on thin-section computed tomography. Am J Respir Crit Care Med 1997;155:1367-75. (Pubitemid 27172785)
-
(1997)
American Journal of Respiratory and Critical Care Medicine
, vol.155
, Issue.4
, pp. 1367-1375
-
-
Wells, A.U.1
King, A.D.2
Rubens, M.B.3
Cramer, D.4
Du Bois, R.M.5
Hansell, D.M.6
-
17
-
-
28144459814
-
High-dose acetylcysteine in idiopathic pulmonary fibrosis
-
DOI 10.1056/NEJMoa042976
-
Demedts M, Behr J, Buhl R, et al. High-dose acetylcysteine in idiopathic pulmonary fibrosis. N Engl J Med 2005;353:2229-42. (Pubitemid 41697286)
-
(2005)
New England Journal of Medicine
, vol.353
, Issue.21
, pp. 2229-2242
-
-
Demedts, M.1
Behr, J.2
Buhl, R.3
Costabel, U.4
Dekhuijzen, R.5
Jansen, H.M.6
MacNee, W.7
Thomeer, M.8
Wallaert, B.9
Laurent, F.10
Nicholson, A.G.11
Verbeken, E.K.12
Verschakelen, J.13
Flower, C.D.R.14
Capron, F.15
Petruzzelli, S.16
De Vuyst, P.17
Van Den Bosch, J.M.M.18
Rodriguez-Becerra, E.19
Corvasce, G.20
Lankhorst, I.21
Sardina, M.22
Montanari, M.23
more..
-
18
-
-
28244500027
-
Antioxidant therapy for idiopathic pulmonary fibrosis
-
DOI 10.1056/NEJMe058210
-
Hunninghake GW. Antioxidant therapy for idiopathic pulmonary fibrosis. N Engl J Med 2005;353: 2285-7. (Pubitemid 41699756)
-
(2005)
New England Journal of Medicine
, vol.353
, Issue.21
, pp. 2285-2287
-
-
Hunninghake, G.W.1
-
19
-
-
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
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