-
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
-
-
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
-
3
-
-
84988924204
-
Predictors of mortality poorly predict common measures of disease progression in idiopathic pulmonary fibrosis
-
Ley B, Bradford WZ, Vittinghoff E, et al. Predictors of mortality poorly predict common measures of disease progression in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2016;194:711-8.
-
(2016)
Am J Respir Crit Care Med
, vol.194
, pp. 711-718
-
-
Ley, B.1
Bradford, W.Z.2
Vittinghoff, E.3
-
4
-
-
84878600828
-
Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis
-
Peljto AL, Zhang Y, Fingerlin TE, et al. Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosis. JAMA 2013;309:2232-9.
-
(2013)
JAMA
, vol.309
, pp. 2232-2239
-
-
Peljto, A.L.1
Zhang, Y.2
Fingerlin, T.E.3
-
5
-
-
85029640399
-
Validation of a 52-gene risk profile for outcome prediction in patients with idiopathic pulmonary fibrosis: An international, multicentre, cohort study
-
Herazo-Maya JD, Sun J, Molyneaux PL, et al. Validation of a 52-gene risk profile for outcome prediction in patients with idiopathic pulmonary fibrosis: an international, multicentre, cohort study. Lancet Respir Med 2017;5:857-68.
-
(2017)
Lancet Respir Med
, vol.5
, pp. 857-868
-
-
Herazo-Maya, J.D.1
Sun, J.2
Molyneaux, P.L.3
-
6
-
-
0036196542
-
Serum surfactant proteins-A and-D as biomarkers in idiopathic pulmonary fibrosis
-
Greene KE, King TE, Kuroki Y, et al. Serum surfactant proteins-A and-D as biomarkers in idiopathic pulmonary fibrosis. Eur Respir J 2002;19:439-46.
-
(2002)
Eur Respir J
, vol.19
, pp. 439-446
-
-
Greene, K.E.1
King, T.E.2
Kuroki, Y.3
-
7
-
-
33644828168
-
Prognostic value of circulating KL-6 in idiopathic pulmonary fibrosis
-
Yokoyama A, Kondo K, Nakajima M, et al. Prognostic value of circulating KL-6 in idiopathic pulmonary fibrosis. Respirology 2006;11:164-8.
-
(2006)
Respirology
, vol.11
, pp. 164-168
-
-
Yokoyama, A.1
Kondo, K.2
Nakajima, M.3
-
8
-
-
43249084804
-
MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis
-
Rosas IO, Richards TJ, Konishi K, et al. MMP1 and MMP7 as potential peripheral blood biomarkers in idiopathic pulmonary fibrosis. PLoS Med 2008;5:e93.
-
(2008)
PLoS Med
, vol.5
, pp. e93
-
-
Rosas, I.O.1
Richards, T.J.2
Konishi, K.3
-
9
-
-
84855264195
-
Peripheral blood proteins predict mortality in idiopathic pulmonary fibrosis
-
Richards TJ, Kaminski N, Baribaud F, et al. Peripheral blood proteins predict mortality in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2012;185:67-76.
-
(2012)
Am J Respir Crit Care Med
, vol.185
, pp. 67-76
-
-
Richards, T.J.1
Kaminski, N.2
Baribaud, F.3
-
10
-
-
85033779884
-
An epithelial biomarker signature for idiopathic pulmonary fibrosis: An analysis from the multicentre PROFILE cohort study
-
Maher TM, Oballa E, Simpson JK, et al. An epithelial biomarker signature for idiopathic pulmonary fibrosis: an analysis from the multicentre PROFILE cohort study. Lancet Respir Med 2017;5:946-55.
-
(2017)
Lancet Respir Med
, vol.5
, pp. 946-955
-
-
Maher, T.M.1
Oballa, E.2
Simpson, J.K.3
-
11
-
-
0024561372
-
Hyaluronan and type III procollagen peptide concentrations in bronchoalveolar lavage fluid in idiopathic pulmonary fibrosis
-
Bjermer L, Lundgren R, Hallgren R. Hyaluronan and type III procollagen peptide concentrations in bronchoalveolar lavage fluid in idiopathic pulmonary fibrosis. Thorax 1989;44:126-31.
-
(1989)
Thorax
, vol.44
, pp. 126-131
-
-
Bjermer, L.1
Lundgren, R.2
Hallgren, R.3
-
12
-
-
84918777951
-
The role of bacteria in the pathogenesis and progression of idiopathic pulmonary fibrosis
-
Molyneaux PL, Cox MJ, Willis-Owen SA, et al. The role of bacteria in the pathogenesis and progression of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2014;190:906-13.
-
(2014)
Am J Respir Crit Care Med
, vol.190
, pp. 906-913
-
-
Molyneaux, P.L.1
Cox, M.J.2
Willis-Owen, S.A.3
-
13
-
-
84903993583
-
Association between lung microbiome and disease progression in IPF: A prospective cohort study
-
Han MK, Zhou Y, Murray S, et al. Association between lung microbiome and disease progression in IPF: a prospective cohort study. Lancet Respir Med 2014;2:548-56.
-
(2014)
Lancet Respir Med
, vol.2
, pp. 548-556
-
-
Han, M.K.1
Zhou, Y.2
Murray, S.3
-
14
-
-
84992602716
-
Texture-based automated quantitative assessment of regional patterns on initial CT in patients with idiopathic pulmonary fibrosis: Relationship to decline in forced vital capacity
-
Park HJ, Lee SM, Song JW, et al. Texture-based automated quantitative assessment of regional patterns on initial CT in patients with idiopathic pulmonary fibrosis: relationship to decline in forced vital capacity. AJR Am J Roentgenol 2016;207:976-83.
-
(2016)
AJR Am J Roentgenol
, vol.207
, pp. 976-983
-
-
Park, H.J.1
Lee, S.M.2
Song, J.W.3
-
15
-
-
85017340618
-
Idiopathic pulmonary fibrosis: The association between the adaptive multiple features method and fibrosis outcomes
-
Salisbury ML, Lynch DA, van Beek EJ, et al. Idiopathic pulmonary fibrosis: the association between the adaptive multiple features method and fibrosis outcomes. Am J Respir Crit Care Med 2017;195:921-9.
-
(2017)
Am J Respir Crit Care Med
, vol.195
, pp. 921-929
-
-
Salisbury, M.L.1
Lynch, D.A.2
Van Beek, E.J.3
-
16
-
-
85051187177
-
Predicting outcomes in idiopathic pulmonary fibrosis using automated CT analysis
-
Epub ahead of print
-
Jacob J, Bartholmai BJ, Rajagopalan S, et al. Predicting outcomes in idiopathic pulmonary fibrosis using automated CT analysis. Am J Respir Crit Care Med 2018. Epub ahead of print.
-
(2018)
Am J Respir Crit Care Med
-
-
Jacob, J.1
Bartholmai, B.J.2
Rajagopalan, S.3
-
17
-
-
84981321016
-
An American Thoracic Society official research statement: Future directions in lung fibrosis research
-
White ES, Borok Z, Brown KK, et al. An American Thoracic Society official research statement: future directions in lung fibrosis research. Am J Respir Crit Care Med 2016;193:792-800.
-
(2016)
Am J Respir Crit Care Med
, vol.193
, pp. 792-800
-
-
White, E.S.1
Borok, Z.2
Brown, K.K.3
-
18
-
-
82755161052
-
Idiopathic pulmonary fibrosis
-
King TE, Pardo A, Selman M. Idiopathic pulmonary fibrosis. Lancet 2011;378:1949-61.
-
(2011)
Lancet
, vol.378
, pp. 1949-1961
-
-
King, T.E.1
Pardo, A.2
Selman, M.3
-
19
-
-
84865113809
-
New cellular and molecular mechanisms of lung injury and fibrosis in idiopathic pulmonary fibrosis
-
Fernandez IE, Eickelberg O. New cellular and molecular mechanisms of lung injury and fibrosis in idiopathic pulmonary fibrosis. Lancet 2012;380:680-8.
-
(2012)
Lancet
, vol.380
, pp. 680-688
-
-
Fernandez, I.E.1
Eickelberg, O.2
-
20
-
-
85046639818
-
Extracellular matrix cross-linking enhances fibroblast growth and protects against matrix proteolysis in lung fibrosis
-
Philp CJ, Siebeke I, Clements D, et al. Extracellular matrix cross-linking enhances fibroblast growth and protects against matrix proteolysis in lung fibrosis. Am J Respir Cell Mol Biol 2018;58:594-603.
-
(2018)
Am J Respir Cell Mol Biol
, vol.58
, pp. 594-603
-
-
Philp, C.J.1
Siebeke, I.2
Clements, D.3
-
21
-
-
84962124806
-
Role of matrix metalloproteinases in the pathogenesis of idiopathic pulmonary fibrosis
-
Pardo A, Cabrera S, Maldonado M, et al. Role of matrix metalloproteinases in the pathogenesis of idiopathic pulmonary fibrosis. Respir Res 2016;17:23.
-
(2016)
Respir Res
, vol.17
, pp. 23
-
-
Pardo, A.1
Cabrera, S.2
Maldonado, M.3
-
22
-
-
84904046300
-
Review article: The efficacy of biomarkers in chronic fibroproliferative diseases-Early diagnosis and prognosis, with liver fibrosis as an exemplar
-
Karsdal MA, Krarup H, Sand JM, et al. Review article: the efficacy of biomarkers in chronic fibroproliferative diseases-early diagnosis and prognosis, with liver fibrosis as an exemplar. Aliment Pharmacol Ther 2014;40:233-49.
-
(2014)
Aliment Pharmacol Ther
, vol.40
, pp. 233-249
-
-
Karsdal, M.A.1
Krarup, H.2
Sand, J.M.3
-
23
-
-
84927692071
-
The role of extracellular matrix quality in pulmonary fibrosis
-
Kristensen JH, Karsdal MA, Genovese F, et al. The role of extracellular matrix quality in pulmonary fibrosis. Respiration 2014;88:487-99.
-
(2014)
Respiration
, vol.88
, pp. 487-499
-
-
Kristensen, J.H.1
Karsdal, M.A.2
Genovese, F.3
-
24
-
-
84930865108
-
Longitudinal change in collagen degradation biomarkers in idiopathic pulmonary fibrosis: An analysis from the prospective, multicentre PROFILE study
-
Jenkins RG, Simpson JK, Saini G, et al. Longitudinal change in collagen degradation biomarkers in idiopathic pulmonary fibrosis: an analysis from the prospective, multicentre PROFILE study. Lancet Respir Med 2015;3:462-72.
-
(2015)
Lancet Respir Med
, vol.3
, pp. 462-472
-
-
Jenkins, R.G.1
Simpson, J.K.2
Saini, G.3
-
25
-
-
49649123154
-
BIBF 1120: Triple angiokinase inhibitor with sustained receptor blockade and good antitumor efficacy
-
Hilberg F, Roth GJ, Krssak M, et al. BIBF 1120: triple angiokinase inhibitor with sustained receptor blockade and good antitumor efficacy. Cancer Res 2008;68:4774-82.
-
(2008)
Cancer Res
, vol.68
, pp. 4774-4782
-
-
Hilberg, F.1
Roth, G.J.2
Krssak, M.3
-
26
-
-
84898792564
-
Antifibrotic and antiinflammatory activity of the tyrosine kinase inhibitor nintedanib in experimental models of lung fibrosis
-
Wollin L, Maillet I, Quesniaux V, et al. Antifibrotic and antiinflammatory activity of the tyrosine kinase inhibitor nintedanib in experimental models of lung fibrosis. J Pharmacol Exp Ther 2014;349:209-20.
-
(2014)
J Pharmacol Exp Ther
, vol.349
, pp. 209-220
-
-
Wollin, L.1
Maillet, I.2
Quesniaux, V.3
-
27
-
-
84928995543
-
Mode of action of nintedanib in the treatment of idiopathic pulmonary fibrosis
-
Wollin L, Wex E, Pautsch A, et al. Mode of action of nintedanib in the treatment of idiopathic pulmonary fibrosis. Eur Respir J 2015;45:1434-45.
-
(2015)
Eur Respir J
, vol.45
, pp. 1434-1445
-
-
Wollin, L.1
Wex, E.2
Pautsch, A.3
-
28
-
-
85014782011
-
Effects of nintedanib on the microvascular architecture in a lung fibrosis model
-
Ackermann M, Kim YO, Wagner WL, et al. Effects of nintedanib on the microvascular architecture in a lung fibrosis model. Angiogenesis 2017;20:359-72.
-
(2017)
Angiogenesis
, vol.20
, pp. 359-372
-
-
Ackermann, M.1
Kim, Y.O.2
Wagner, W.L.3
-
29
-
-
80053091084
-
Efficacy of a tyrosine kinase inhibitor in idiopathic pulmonary fibrosis
-
Richeldi L, Costabel U, Selman M, et al. Efficacy of a tyrosine kinase inhibitor in idiopathic pulmonary fibrosis. N Engl J Med 2011;365:1079-87.
-
(2011)
N Engl J Med
, vol.365
, pp. 1079-1087
-
-
Richeldi, L.1
Costabel, U.2
Selman, M.3
-
30
-
-
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
Dubois, R.M.2
Raghu, G.3
-
32
-
-
0025886867
-
The St George's respiratory questionnaire
-
discussion 33-37
-
Jones PW, Quirk FH, Baveystock CM. The St George's respiratory questionnaire. Respir Med 1991;85 Suppl B(Suppl B):25-31. discussion 33-37.
-
(1991)
Respir Med
, vol.85
, pp. 25-31
-
-
Jones, P.W.1
Quirk, F.H.2
Baveystock, C.M.3
-
33
-
-
0031912648
-
Validation of a new dyspnea measure: The UCSD Shortness of Breath Questionnaire. University of California, San Diego
-
Eakin EG, Resnikoff PM, Prewitt LM, et al. Validation of a new dyspnea measure: the UCSD Shortness of Breath Questionnaire. University of California, San Diego. Chest 1998;113:619-24.
-
(1998)
Chest
, vol.113
, pp. 619-624
-
-
Eakin, E.G.1
Resnikoff, P.M.2
Prewitt, L.M.3
-
34
-
-
79952943038
-
Pharmacokinetics and metabolism of BIBF 1120 after oral dosing to healthy male volunteers
-
Stopfer P, Rathgen K, Bischoff D, et al. Pharmacokinetics and metabolism of BIBF 1120 after oral dosing to healthy male volunteers. Xenobiotica 2011;41:297-311.
-
(2011)
Xenobiotica
, vol.41
, pp. 297-311
-
-
Stopfer, P.1
Rathgen, K.2
Bischoff, D.3
-
35
-
-
84988258715
-
Effect of baseline FVC on lung function decline with nintedanib in patients with IPF
-
Maher TM, Flaherty KR, Noble PW, et al. Effect of baseline FVC on lung function decline with nintedanib in patients with IPF. Eur Respir J 2015;46(Suppl. 59):OA4499.
-
(2015)
Eur Respir J
, vol.46
, pp. OA4499
-
-
Maher, T.M.1
Flaherty, K.R.2
Noble, P.W.3
-
36
-
-
85017017908
-
Nintedanib in patients with idiopathic pulmonary fibrosis and preserved lung volume
-
Kolb M, Richeldi L, Behr J, et al. Nintedanib in patients with idiopathic pulmonary fibrosis and preserved lung volume. Thorax 2017;72:340-6.
-
(2017)
Thorax
, vol.72
, pp. 340-346
-
-
Kolb, M.1
Richeldi, L.2
Behr, J.3
-
37
-
-
85029359255
-
Acute exacerbation and decline in forced vital capacity are associated with increased mortality in idiopathic pulmonary fibrosis
-
Paterniti MO, Bi Y, Rekić D, et al. Acute exacerbation and decline in forced vital capacity are associated with increased mortality in idiopathic pulmonary fibrosis. Ann Am Thorac Soc 2017;14:1395-402.
-
(2017)
Ann Am Thorac Soc
, vol.14
, pp. 1395-1402
-
-
Paterniti, M.O.1
Bi, Y.2
Rekić, D.3
-
38
-
-
84992313036
-
Daily home spirometry: An effective tool for detecting progression in idiopathic pulmonary fibrosis
-
Russell AM, Adamali H, Molyneaux PL, et al. Daily home spirometry: an effective tool for detecting progression in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2016;194:989-97.
-
(2016)
Am J Respir Crit Care Med
, vol.194
, pp. 989-997
-
-
Russell, A.M.1
Adamali, H.2
Molyneaux, P.L.3
-
39
-
-
85026260747
-
Home monitoring improves endpoint efficiency in idiopathic pulmonary fibrosis
-
Johannson KA, Vittinghoff E, Morisset J, et al. Home monitoring improves endpoint efficiency in idiopathic pulmonary fibrosis. Eur Respir J 2017;50:1602406.
-
(2017)
Eur Respir J
, vol.50
, pp. 1602406
-
-
Johannson, K.A.1
Vittinghoff, E.2
Morisset, J.3
|