-
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
-
-
77951176799
-
Idiopathic pulmonary fibrosis: A disease with similarities and links to cancer biology
-
Vancheri C, Failla M, Crimi N, et al. Idiopathic pulmonary fibrosis: a disease with similarities and links to cancer biology. Eur Respir J 2010; 35: 496-504.
-
(2010)
Eur Respir J
, vol.35
, pp. 496-504
-
-
Vancheri, C.1
Failla, M.2
Crimi, N.3
-
3
-
-
70349422341
-
Increased local expression of coagulation factor X contributes to the fibrotic response in human and murine lung injury
-
Scotton CJ, Krupiczojc MA, Königshoff M, et al. Increased local expression of coagulation factor X contributes to the fibrotic response in human and murine lung injury. J Clin Invest 2009; 119: 2550-2563.
-
(2009)
J Clin Invest
, vol.119
, pp. 2550-2563
-
-
Scotton, C.J.1
Krupiczojc, M.A.2
Königshoff, M.3
-
4
-
-
33744914050
-
Evolving concepts of apoptosis in idiopathic pulmonary fibrosis
-
Thannickal VJ, Horowitz JC. Evolving concepts of apoptosis in idiopathic pulmonary fibrosis. Proc Am Thorac Soc 2006; 3: 350-356.
-
(2006)
Proc Am Thorac Soc
, vol.3
, pp. 350-356
-
-
Thannickal, V.J.1
Horowitz, J.C.2
-
5
-
-
37549007538
-
Apoptosis in pulmonary fibrosis: Too much or not enough?
-
Fattman CL. Apoptosis in pulmonary fibrosis: too much or not enough? Antioxid Redox Signal 2008; 10: 379-385.
-
(2008)
Antioxid Redox Signal
, vol.10
, pp. 379-385
-
-
Fattman, C.L.1
-
6
-
-
69949114515
-
NADPH oxidase-4 mediates myofibroblast activation and fibrogenic responses to lung injury
-
Hecker L, Vittal R, Jones T, et al. NADPH oxidase-4 mediates myofibroblast activation and fibrogenic responses to lung injury. Nat Med 2009; 15: 1077-1081.
-
(2009)
Nat Med
, vol.15
, pp. 1077-1081
-
-
Hecker, L.1
Vittal, R.2
Jones, T.3
-
7
-
-
33744924735
-
Role of epithelial cells in idiopathic pulmonary fibrosis: From innocent targets to serial killers
-
Selman M, Pardo A. Role of epithelial cells in idiopathic pulmonary fibrosis: from innocent targets to serial killers. Proc Am Thorac Soc 2006; 3: 364-372.
-
(2006)
Proc Am Thorac Soc
, vol.3
, pp. 364-372
-
-
Selman, M.1
Pardo, A.2
-
8
-
-
17844384822
-
Induction of epithelial-mesenchymal transition in alveolar epithelial cells by transforming growth factor-beta1: Potential role in idiopathic pulmonary fibrosis
-
Willis BC, Liebler JM, Luby-Phelps K, et al. Induction of epithelial-mesenchymal transition in alveolar epithelial cells by transforming growth factor-beta1: potential role in idiopathic pulmonary fibrosis. Am J Pathol 2005; 166: 1321-1332.
-
(2005)
Am J Pathol
, vol.166
, pp. 1321-1332
-
-
Willis, B.C.1
Liebler, J.M.2
Luby-Phelps, K.3
-
9
-
-
59449090107
-
TGF-beta-induced epithelial to mesenchymal transition
-
Xu J, Lamouille S, Derynck R. TGF-beta-induced epithelial to mesenchymal transition. Cell Res 2009; 19: 156-172.
-
(2009)
Cell Res
, vol.19
, pp. 156-172
-
-
Xu, J.1
Lamouille, S.2
Derynck, R.3
-
10
-
-
33748375828
-
Alveolar epithelial cell mesenchymal transition develops in vivo during pulmonary fibrosis and is regulated by the extracellular matrix
-
Kim KK, Kugler MC, Wolters PJ, et al. Alveolar epithelial cell mesenchymal transition develops in vivo during pulmonary fibrosis and is regulated by the extracellular matrix. Proc Natl Acad Sci USA 2006; 103: 13180-13185.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 13180-13185
-
-
Kim, K.K.1
Kugler, M.C.2
Wolters, P.J.3
-
11
-
-
72949119709
-
SNAI transcription factors mediate epithelial-mesenchymal transition in lung fibrosis
-
Jayachandran A, Königshoff M, Yu H, et al. SNAI transcription factors mediate epithelial-mesenchymal transition in lung fibrosis. Thorax 2009; 64: 1053-1061.
-
(2009)
Thorax
, vol.64
, pp. 1053-1061
-
-
Jayachandran, A.1
Königshoff, M.2
Yu, H.3
-
12
-
-
77955399498
-
Inhibition and role of let-7d in idiopathic pulmonary fibrosis
-
Pandit KV, Corcoran D, Yousef H, et al. Inhibition and role of let-7d in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2010; 182: 220-229.
-
(2010)
Am J Respir Crit Care Med
, vol.182
, pp. 220-229
-
-
Pandit, K.V.1
Corcoran, D.2
Yousef, H.3
-
13
-
-
28144459814
-
High-dose acetylcysteine in idiopathic pulmonary fibrosis
-
Demedts M, Behr J, Buhl R, et al. High-dose acetylcysteine in idiopathic pulmonary fibrosis. N Engl J Med 2005; 353: 2229-2242.
-
(2005)
N Engl J Med
, vol.353
, pp. 2229-2242
-
-
Demedts, M.1
Behr, J.2
Buhl, R.3
-
14
-
-
73949096392
-
Lung function in idiopathic pulmonary fibrosis-extended analyses of the IFIGENIA trial
-
Behr J, Demedts M, Buhl R, et al. Lung function in idiopathic pulmonary fibrosis-extended analyses of the IFIGENIA trial. Respir Res 2009; 10: 101.
-
(2009)
Respir Res
, vol.10
, pp. 101
-
-
Behr, J.1
Demedts, M.2
Buhl, R.3
-
16
-
-
66349113736
-
Hepatocyte growth factor inhibits epithelial to myofibroblast transition in lung cells via Smad7
-
Shukla MN, Rose JL, Ray R, et al. Hepatocyte growth factor inhibits epithelial to myofibroblast transition in lung cells via Smad7. Am J Respir Cell Mol Biol 2009; 40: 643-653.
-
(2009)
Am J Respir Cell Mol Biol
, vol.40
, pp. 643-653
-
-
Shukla, M.N.1
Rose, J.L.2
Ray, R.3
-
17
-
-
48949117344
-
Fibrocytes are a potential source of lung fibroblasts in idiopathic pulmonary fibrosis
-
Andersson-Sjöland A, de Alba CG, Nihlberg K, et al. Fibrocytes are a potential source of lung fibroblasts in idiopathic pulmonary fibrosis. Int J Biochem Cell Biol 2008; 40: 2129-2140.
-
(2008)
Int J Biochem Cell Biol
, vol.40
, pp. 2129-2140
-
-
Andersson-Sjöland, A.1
de Alba, C.G.2
Nihlberg, K.3
-
18
-
-
70350738517
-
The role of circulating mesenchymal progenitor cells (fibrocytes) in the pathogenesis of pulmonary fibrosis
-
Strieter RM, Keeley EC, Hughes MA, et al. The role of circulating mesenchymal progenitor cells (fibrocytes) in the pathogenesis of pulmonary fibrosis. J Leukoc Biol 2009; 86: 1111-1118.
-
(2009)
J Leukoc Biol
, vol.86
, pp. 1111-1118
-
-
Strieter, R.M.1
Keeley, E.C.2
Hughes, M.A.3
-
19
-
-
4043055316
-
Circulating fibrocytes traffic to the lungs in response to CXCL12 and mediate fibrosis
-
Phillips RJ, Burdick MD, Hong K, et al. Circulating fibrocytes traffic to the lungs in response to CXCL12 and mediate fibrosis. J Clin Invest 2004; 114: 438-446.
-
(2004)
J Clin Invest
, vol.114
, pp. 438-446
-
-
Phillips, R.J.1
Burdick, M.D.2
Hong, K.3
-
20
-
-
77956338352
-
Investigation of bone marrow mesenchymal stem cells (BM MSCs) involvement in idiopathic pulmonary fibrosis (IPF)
-
Antoniou KM, Papadaki HA, Soufla G, et al. Investigation of bone marrow mesenchymal stem cells (BM MSCs) involvement in idiopathic pulmonary fibrosis (IPF). Respir Med 2010; 104: 1535-1542.
-
(2010)
Respir Med
, vol.104
, pp. 1535-1542
-
-
Antoniou, K.M.1
Papadaki, H.A.2
Soufla, G.3
-
21
-
-
0242500879
-
Aberrant Wnt/beta-catenin pathway activation in idiopathic pulmonary fibrosis
-
Chilosi M, Poletti V, Zamò A, et al. Aberrant Wnt/beta-catenin pathway activation in idiopathic pulmonary fibrosis. Am J Pathol 2003; 162: 1495-1502.
-
(2003)
Am J Pathol
, vol.162
, pp. 1495-1502
-
-
Chilosi, M.1
Poletti, V.2
Zamò, A.3
-
22
-
-
47749101725
-
Functional Wnt signaling is increased in idiopathic pulmonary fibrosis
-
Königshoff M, Balsara N, Pfaff EM, et al. Functional Wnt signaling is increased in idiopathic pulmonary fibrosis. PLoS One 2008; 3: e2142.
-
(2008)
PLoS One
, vol.e2142
, pp. 3
-
-
Königshoff, M.1
Balsara, N.2
Pfaff, E.M.3
-
23
-
-
65249088418
-
WNT1-inducible signaling protein-1 mediates pulmonary fibrosis in mice and is upregulated in humans with idiopathic pulmonary fibrosis
-
Königshoff M, Kramer M, Balsara N, et al. WNT1-inducible signaling protein-1 mediates pulmonary fibrosis in mice and is upregulated in humans with idiopathic pulmonary fibrosis. J Clin Invest 2009; 119: 772-787.
-
(2009)
J Clin Invest
, vol.119
, pp. 772-787
-
-
Königshoff, M.1
Kramer, M.2
Balsara, N.3
-
24
-
-
33745183811
-
vbeta6 integrin-dependent TGF-beta activation and promotes acute lung injury
-
Jenkins RG, Su X, Su G, et al. Ligation of protease-activated receptor 1 enhances alphavbeta6 integrin-dependent TGF-beta activation and promotes acute lung injury. J Clin Invest 2006; 116: 1606-1614.
-
(2006)
J Clin Invest
, vol.116
, pp. 1606-1614
-
-
Jenkins, R.G.1
Su, X.2
Su, G.3
-
25
-
-
65349145784
-
q
-
Xu MY, Porte J, Knox AJ, et al. Lysophosphatidic acid induces alphavbeta6 integrin-mediated TGF-beta activation via the LPA2 receptor and the small G protein G alphaq. Am J Pathol 2009; 174: 1264-1279.
-
(2009)
Am J Pathol
, vol.174
, pp. 1264-1279
-
-
Xu, M.Y.1
Porte, J.2
Knox, A.J.3
-
26
-
-
0033524949
-
The integrin alpha v beta 6 binds and activates latent TGF beta 1: A mechanism for regulating pulmonary inflammation and fibrosis
-
Munger JS, Huang X, Kawakatsu H, et al. The integrin alpha v beta 6 binds and activates latent TGF beta 1: a mechanism for regulating pulmonary inflammation and fibrosis. Cell 1999; 96: 319-328.
-
(1999)
Cell
, vol.96
, pp. 319-328
-
-
Munger, J.S.1
Huang, X.2
Kawakatsu, H.3
-
27
-
-
38049002642
-
vbeta6 prevents pulmonary fibrosis without exacerbating inflammation
-
Horan GS, Wood S, Ona V, et al. Partial inhibition of integrin alphavbeta6 prevents pulmonary fibrosis without exacerbating inflammation. Am J Respir Crit Care Med 2008; 177: 56-65.
-
(2008)
Am J Respir Crit Care Med
, vol.177
, pp. 56-65
-
-
Horan, G.S.1
Wood, S.2
Ona, V.3
-
28
-
-
37849008770
-
vbeta6, an activator of latent transforming growth factor-beta, prevents radiation-induced lung fibrosis
-
Puthawala K, Hadjiangelis N, Jacoby SC, et al. Inhibition of integrin alphavbeta6, an activator of latent transforming growth factor-beta, prevents radiation-induced lung fibrosis. Am J Respir Crit Care Med 2008; 177: 82-90.
-
(2008)
Am J Respir Crit Care Med
, vol.177
, pp. 82-90
-
-
Puthawala, K.1
Hadjiangelis, N.2
Jacoby, S.C.3
-
29
-
-
0036119338
-
Molecular, pharmacological and functional diversity of 5-HT receptors
-
Hoyer D, Hannon JP, Martin GR. Molecular, pharmacological and functional diversity of 5-HT receptors. Pharmacol Biochem Behav 2002; 71: 533-554.
-
(2002)
Pharmacol Biochem Behav
, vol.71
, pp. 533-554
-
-
Hoyer, D.1
Hannon, J.P.2
Martin, G.R.3
-
30
-
-
78149303247
-
Increased expression of 5-hydroxytryptamine2A/B receptors in idiopathic pulmonary fibrosis: A rationale for therapeutic intervention
-
Königshoff M, Dumitrascu R, Udalov S, et al. Increased expression of 5-hydroxytryptamine2A/B receptors in idiopathic pulmonary fibrosis: a rationale for therapeutic intervention. Thorax 2010; 65: 949-955.
-
(2010)
Thorax
, vol.65
, pp. 949-955
-
-
Königshoff, M.1
Dumitrascu, R.2
Udalov, S.3
-
31
-
-
33744970745
-
Transgenic mice over-expressing the 5-hydroxytryptamine transporter gene in smooth muscle develop pulmonary hypertension
-
Guignabert C, Izikki M, Tu LI, et al. Transgenic mice over-expressing the 5-hydroxytryptamine transporter gene in smooth muscle develop pulmonary hypertension. Circ Res 2006; 98: 1323-1330.
-
(2006)
Circ Res
, vol.98
, pp. 1323-1330
-
-
Guignabert, C.1
Izikki, M.2
Tu, L.I.3
-
32
-
-
23644461803
-
Oxidative stress in pulmonary fibrosis: A possible role for redox modulatory therapy
-
Kinnula VL, Fattman CL, Tan RJ, et al. Oxidative stress in pulmonary fibrosis: a possible role for redox modulatory therapy. Am J Respir Crit Care Med 2005; 172: 417-422.
-
(2005)
Am J Respir Crit Care Med
, vol.172
, pp. 417-422
-
-
Kinnula, V.L.1
Fattman, C.L.2
Tan, R.J.3
-
33
-
-
38049079133
-
Serum levels of oxidative stress as a marker of disease severity in idiopathic pulmonary fibrosis
-
Daniil ZD, Papageorgiou E, Koutsokera A, et al. Serum levels of oxidative stress as a marker of disease severity in idiopathic pulmonary fibrosis. Pulm Pharmacol Ther 2008; 21: 26-31.
-
(2008)
Pulm Pharmacol Ther
, vol.21
, pp. 26-31
-
-
Daniil, Z.D.1
Papageorgiou, E.2
Koutsokera, A.3
-
34
-
-
0029148261
-
Increased oxidation of extracellular glutathione by bronchoalveolar inflammatory cells in diffuse fibrosing alveolitis
-
Behr J, Degenkolb B, Maier K, et al. Increased oxidation of extracellular glutathione by bronchoalveolar inflammatory cells in diffuse fibrosing alveolitis. Eur Respir J 1995; 8: 1286-1292.
-
(1995)
Eur Respir J
, vol.8
, pp. 1286-1292
-
-
Behr, J.1
Degenkolb, B.2
Maier, K.3
-
35
-
-
0024578662
-
Glutathione deficiency in the epithelial lining fluid of the lower respiratory tract in idiopathic pulmonary fibrosis
-
Cantin AM, Hubbard RC, Crystal RG. Glutathione deficiency in the epithelial lining fluid of the lower respiratory tract in idiopathic pulmonary fibrosis. Am Rev Respir Dis 1989; 139: 370-372.
-
(1989)
Am Rev Respir Dis
, vol.139
, pp. 370-372
-
-
Cantin, A.M.1
Hubbard, R.C.2
Crystal, R.G.3
-
36
-
-
0031280268
-
Transforming growth factor-beta1 is a potent inhibitor of glutathione synthesis in the lung epithelial cell line A549: Transcriptional effect on the GSH rate-limiting enzyme gamma-glutamylcysteine synthetase
-
Arsalane K, Dubois CM, Muanza T, et al. Transforming growth factor-beta1 is a potent inhibitor of glutathione synthesis in the lung epithelial cell line A549: transcriptional effect on the GSH rate-limiting enzyme gamma-glutamylcysteine synthetase. Am J Respir Cell Mol Biol 1997; 17: 599-607.
-
(1997)
Am J Respir Cell Mol Biol
, vol.17
, pp. 599-607
-
-
Arsalane, K.1
Dubois, C.M.2
Muanza, T.3
-
37
-
-
0031449645
-
Antioxidative and clinical effects of high-dose N-acetylcysteine in fibrosing alveolitis. Adjunctive therapy to maintenance immunosuppression
-
Behr J, Maier K, Degenkolb B, et al. Antioxidative and clinical effects of high-dose N-acetylcysteine in fibrosing alveolitis. Adjunctive therapy to maintenance immunosuppression. Am J Respir Crit Care Med 1997; 156: 1897-1901.
-
(1997)
Am J Respir Crit Care Med
, vol.156
, pp. 1897-1901
-
-
Behr, J.1
Maier, K.2
Degenkolb, B.3
-
38
-
-
0036014536
-
Intracellular glutathione and bronchoalveolar cells in fibrosing alveolitis: Effects of N-acetylcysteine
-
Behr J, Degenkolb B, Krombach F, et al. Intracellular glutathione and bronchoalveolar cells in fibrosing alveolitis: effects of N-acetylcysteine. Eur Respir J 2002; 19: 906-911.
-
(2002)
Eur Respir J
, vol.19
, pp. 906-911
-
-
Behr, J.1
Degenkolb, B.2
Krombach, F.3
-
39
-
-
0035198813
-
Ceramide-mediated apoptosis in lung epithelial cells is regulated by glutathione
-
Lavrentiadou SN, Chan C, Kawcak T, et al. Ceramide-mediated apoptosis in lung epithelial cells is regulated by glutathione. Am J Respir Cell Mol Biol 2001; 25: 676-684.
-
(2001)
Am J Respir Cell Mol Biol
, vol.25
, pp. 676-684
-
-
Lavrentiadou, S.N.1
Chan, C.2
Kawcak, T.3
-
40
-
-
71249107919
-
N-acetyl-L-cysteine inhibits TGF-beta1-induced profibrotic responses in fibroblasts
-
Sugiura H, Ichikawa T, Liu X, et al. N-acetyl-L-cysteine inhibits TGF-beta1-induced profibrotic responses in fibroblasts. Pulm Pharmacol Ther 2009; 22: 487-491.
-
(2009)
Pulm Pharmacol Ther
, vol.22
, pp. 487-491
-
-
Sugiura, H.1
Ichikawa, T.2
Liu, X.3
-
41
-
-
77950829907
-
N-acetylcysteine inhibits IL-8 and MMP-9 release and ICAM-1 expression by bronchoalveolar cells from interstitial lung disease patients
-
Radomska-Leśniewska DM, Skopińska-Rózewska E, Jankowska-Steifer E, et al. N-acetylcysteine inhibits IL-8 and MMP-9 release and ICAM-1 expression by bronchoalveolar cells from interstitial lung disease patients. Pharmacol Rep 2010; 62: 131-138.
-
(2010)
Pharmacol Rep
, vol.62
, pp. 131-138
-
-
Radomska-Leśniewska, D.M.1
Skopińska-Rózewska, E.2
Jankowska-Steifer, E.3
-
42
-
-
77955881563
-
Diminished prostaglan-din E2 contributes to the apoptosis paradox in idiopathic pulmonary fibrosis
-
Maher TM, Evans IC, Bottoms SE, et al. Diminished prostaglan-din E2 contributes to the apoptosis paradox in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2010; 182: 73-82.
-
(2010)
Am J Respir Crit Care Med
, vol.182
, pp. 73-82
-
-
Maher, T.M.1
Evans, I.C.2
Bottoms, S.E.3
-
43
-
-
70349115049
-
Endothelin-1 and transforming growth factor-beta1 independently induce fibro-blast resistance to apoptosis via AKT activation
-
Kulasekaran P, Scavone CA, Rogers DS, et al. Endothelin-1 and transforming growth factor-beta1 independently induce fibro-blast resistance to apoptosis via AKT activation. Am J Respir Cell Mol Biol 2009; 41: 484-493.
-
(2009)
Am J Respir Cell Mol Biol
, vol.41
, pp. 484-493
-
-
Kulasekaran, P.1
Scavone, C.A.2
Rogers, D.S.3
-
44
-
-
30344485686
-
Negative regulation of myofibroblast differentiation by PTEN (Phosphatase and Tensin Homolog Deleted on chromosome 10)
-
White ES, Atrasz RG, Hu B, et al. Negative regulation of myofibroblast differentiation by PTEN (Phosphatase and Tensin Homolog Deleted on chromosome 10). Am J Respir Crit Care Med 2006; 173: 112-121.
-
(2006)
Am J Respir Crit Care Med
, vol.173
, pp. 112-121
-
-
White, E.S.1
Atrasz, R.G.2
Hu, B.3
-
46
-
-
33646481327
-
Cutting edge: Nonproliferating mature immune cells form a novel type of organized lymphoid structure in idiopathic pulmonary fibrosis
-
Marchal-Sommé J, Uzunhan Y, Marchand-Adam S, et al. Cutting edge: nonproliferating mature immune cells form a novel type of organized lymphoid structure in idiopathic pulmonary fibrosis. J Immunol 2006; 176: 5735-5739.
-
(2006)
J Immunol
, vol.176
, pp. 5735-5739
-
-
Marchal-Sommé, J.1
Uzunhan, Y.2
Marchand-Adam, S.3
-
47
-
-
34848884629
-
Cellular and humoral autoreactivity in idiopathic pulmonary fibrosis
-
Feghali-Bostwick CA, Tsai CG, Valentine VG, et al. Cellular and humoral autoreactivity in idiopathic pulmonary fibrosis. J Immunol 2007; 179: 2592-2599.
-
(2007)
J Immunol
, vol.179
, pp. 2592-2599
-
-
Feghali-Bostwick, C.A.1
Tsai, C.G.2
Valentine, V.G.3
-
48
-
-
79952719285
-
Identification of periplakin as a new target for autoreactivity in idiopathic pulmonary fibrosis
-
Taillé C, Grootenboer-Mignot S, Boursier C, et al. Identification of periplakin as a new target for autoreactivity in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2011; 183: 759-766.
-
(2011)
Am J Respir Crit Care Med
, vol.183
, pp. 759-766
-
-
Taillé, C.1
Grootenboer-Mignot, S.2
Boursier, C.3
-
49
-
-
52949084684
-
Factor Xa: At the crossroads between coagulation and signaling in physiology and disease
-
Borensztajn K, Peppelenbosch MP, Spek CA. Factor Xa: at the crossroads between coagulation and signaling in physiology and disease. Trends Mol Med 2008; 14: 429-440.
-
(2008)
Trends Mol Med
, vol.14
, pp. 429-440
-
-
Borensztajn, K.1
Peppelenbosch, M.P.2
Spek, C.A.3
-
50
-
-
0032126368
-
Thrombin stimulates fibroblast procollagen production via proteolytic activation of protease-activated receptor 1
-
Chambers RC, Dabbagh K, McAnulty RJ, et al. Thrombin stimulates fibroblast procollagen production via proteolytic activation of protease-activated receptor 1. Biochem J 1998; 333: 121-127.
-
(1998)
Biochem J
, vol.333
, pp. 121-127
-
-
Chambers, R.C.1
Dabbagh, K.2
McAnulty, R.J.3
-
51
-
-
63349085645
-
Pulmonary epithelium is a prominent source of proteinase-activated receptor-1-inducible CCL2 in pulmonary fibrosis
-
Mercer PF, Johns RH, Scotton CJ, et al. Pulmonary epithelium is a prominent source of proteinase-activated receptor-1-inducible CCL2 in pulmonary fibrosis. Am J Respir Crit Care Med 2009; 179: 414-425.
-
(2009)
Am J Respir Crit Care Med
, vol.179
, pp. 414-425
-
-
Mercer, P.F.1
Johns, R.H.2
Scotton, C.J.3
-
52
-
-
0034634622
-
Thrombin is a potent inducer of connective tissue growth factor production via proteolytic activation of protease-activated receptor-1
-
Chambers RC, Leoni P, Blanc-Brude OP, et al. Thrombin is a potent inducer of connective tissue growth factor production via proteolytic activation of protease-activated receptor-1. J Biol Chem 2000; 275: 35584-35591.
-
(2000)
J Biol Chem
, vol.275
, pp. 35584-35591
-
-
Chambers, R.C.1
Leoni, P.2
Blanc-Brude, O.P.3
-
53
-
-
2942644636
-
Inter-observer variation between pathologists in diffuse parenchymal lung disease
-
Nicholson AG, Addis BJ, Bharucha H, et al. Inter-observer variation between pathologists in diffuse parenchymal lung disease. Thorax 2004; 59: 500-505.
-
(2004)
Thorax
, vol.59
, pp. 500-505
-
-
Nicholson, A.G.1
Addis, B.J.2
Bharucha, H.3
-
54
-
-
0035508478
-
Histopathologic variability in usual and nonspecific interstitial pneumonias
-
Flaherty KR, Travis WD, Colby TV, et al. Histopathologic variability in usual and nonspecific interstitial pneumonias. Am J Respir Crit Care Med 2001; 164: 1722-1727.
-
(2001)
Am J Respir Crit Care Med
, vol.164
, pp. 1722-1727
-
-
Flaherty, K.R.1
Travis, W.D.2
Colby, T.V.3
-
55
-
-
1242351701
-
Prognostic implications of histologic patterns in multiple surgical lung biopsies from patients with idiopathic interstitial pneumonias
-
Monaghan H, Wells AU, Colby TV, et al. Prognostic implications of histologic patterns in multiple surgical lung biopsies from patients with idiopathic interstitial pneumonias. Chest 2004; 125: 522-526.
-
(2004)
Chest
, vol.125
, pp. 522-526
-
-
Monaghan, H.1
Wells, A.U.2
Colby, T.V.3
-
56
-
-
5144222998
-
Idiopathic interstitial pneumonia: What is the effect of a multidisciplinary approach to diagnosis?
-
Flaherty KR, King TE, Raghu G, et al. Idiopathic interstitial pneumonia: what is the effect of a multidisciplinary approach to diagnosis? Am J Respir Crit Care Med 2004; 170: 904-910.
-
(2004)
Am J Respir Crit Care Med
, vol.170
, pp. 904-910
-
-
Flaherty, K.R.1
King, T.E.2
Raghu, G.3
-
57
-
-
0035185842
-
Nonspecific interstitial pneumonia and usual interstitial pneumonia: Comparative appearances at and diagnostic accuracy of thin-section CT
-
MacDonald SL, Rubens MB, Hansell DM, et al. Nonspecific interstitial pneumonia and usual interstitial pneumonia: comparative appearances at and diagnostic accuracy of thin-section CT. Radiology 2001; 221: 600-605.
-
(2001)
Radiology
, vol.221
, pp. 600-605
-
-
Macdonald, S.L.1
Rubens, M.B.2
Hansell, D.M.3
-
58
-
-
63849343420
-
Pivotal clinical dilemmas in collagen vascular diseases associated with interstitial lung involvement
-
Antoniou KM, Margaritopoulos G, Economidou F, et al. Pivotal clinical dilemmas in collagen vascular diseases associated with interstitial lung involvement. Eur Respir J 2009; 33: 882-896.
-
(2009)
Eur Respir J
, vol.33
, pp. 882-896
-
-
Antoniou, K.M.1
Margaritopoulos, G.2
Economidou, F.3
-
59
-
-
77957948534
-
Diffuse interstitial lung disease: Overlaps and uncertainties
-
Walsh SL, Hansell DM. Diffuse interstitial lung disease: overlaps and uncertainties. Eur Radiol 2010; 20: 1859-1867.
-
(2010)
Eur Radiol
, vol.20
, pp. 1859-1867
-
-
Walsh, S.L.1
Hansell, D.M.2
-
60
-
-
0032717980
-
Respiratory bronchio-litis, respiratory bronchiolitis-associated interstitial lung disease, and desquamative interstitial pneumonia: Different entities or part of the spectrum of the same disease process?
-
Heyneman LE, Ward S, Lynch DA, et al. Respiratory bronchio-litis, respiratory bronchiolitis-associated interstitial lung disease, and desquamative interstitial pneumonia: different entities or part of the spectrum of the same disease process? AJR Am J Roentgenol 1999; 173: 1617-1622.
-
(1999)
AJR Am J Roentgenol
, vol.173
, pp. 1617-1622
-
-
Heyneman, L.E.1
Ward, S.2
Lynch, D.A.3
-
62
-
-
0029066559
-
Nonspecific interstitial pneumonia with fibrosis: Radiographic and CT findings in seven patients
-
Park JS, Lee KS, Kim JS, et al. Nonspecific interstitial pneumonia with fibrosis: radiographic and CT findings in seven patients. Radiology 1995; 195: 645-648.
-
(1995)
Radiology
, vol.195
, pp. 645-648
-
-
Park, J.S.1
Lee, K.S.2
Kim, J.S.3
-
63
-
-
0031793935
-
Nonspecific interstitial pneumonia. Individualization of a clinicopathologic entity in a series of 12 patients
-
Cottin V, Donsbeck AV, Revel D, et al. Nonspecific interstitial pneumonia. Individualization of a clinicopathologic entity in a series of 12 patients. Am J Respir Crit Care Med 1998; 158: 1286-1293.
-
(1998)
Am J Respir Crit Care Med
, vol.158
, pp. 1286-1293
-
-
Cottin, V.1
Donsbeck, A.V.2
Revel, D.3
-
64
-
-
0025274632
-
Interstitial lung disease in polymyositis and dermatomyositis. Clinical features and prognosis as correlated with histologic findings
-
Tazelaar HD, Viggiano RW, Pickersgill J, et al. Interstitial lung disease in polymyositis and dermatomyositis. Clinical features and prognosis as correlated with histologic findings. Am Rev Respir Dis 1990; 141: 727-733.
-
(1990)
Am Rev Respir Dis
, vol.141
, pp. 727-733
-
-
Tazelaar, H.D.1
Viggiano, R.W.2
Pickersgill, J.3
-
65
-
-
0030845006
-
Pulmonary involvement in polymyositis and dermatomyositis: Sequential evaluation with CT
-
Mino M, Noma S, Taguchi Y, et al. Pulmonary involvement in polymyositis and dermatomyositis: sequential evaluation with CT. AJR Am J Roentgenol 1997; 169: 83-87.
-
(1997)
AJR Am J Roentgenol
, vol.169
, pp. 83-87
-
-
Mino, M.1
Noma, S.2
Taguchi, Y.3
-
66
-
-
78349261541
-
Alveolar proteinosis with hypersensitivity pneumonitis: A new clinical phenotype
-
Verma H, Nicholson AG, Kerr KM, et al. Alveolar proteinosis with hypersensitivity pneumonitis: a new clinical phenotype. Respirology 2010; 15: 1197-1202.
-
(2010)
Respirology
, vol.15
, pp. 1197-1202
-
-
Verma, H.1
Nicholson, A.G.2
Kerr, K.M.3
-
67
-
-
0031934678
-
The significance of bronchial dilatation on CT in patients with adult respiratory distress syndrome
-
Howling SJ, Evans TW, Hansell DM. The significance of bronchial dilatation on CT in patients with adult respiratory distress syndrome. Clin Radiol 1998; 53: 105-109.
-
(1998)
Clin Radiol
, vol.53
, pp. 105-109
-
-
Howling, S.J.1
Evans, T.W.2
Hansell, D.M.3
-
68
-
-
0028140298
-
Nonspecific interstitial pneumonia/ fibrosis. Histologic features and clinical significance
-
Katzenstein AL, Fiorelli RF. Nonspecific interstitial pneumonia/ fibrosis. Histologic features and clinical significance. Am J Surg Pathol 1994; 18: 136-147.
-
(1994)
Am J Surg Pathol
, vol.18
, pp. 136-147
-
-
Katzenstein, A.L.1
Fiorelli, R.F.2
-
69
-
-
78449269444
-
The clinical utility of bronchoalveolar lavage in diffuse parenchymal lung disease
-
Wells AU. The clinical utility of bronchoalveolar lavage in diffuse parenchymal lung disease. Eur Respir Rev 2010; 19: 237-241.
-
(2010)
Eur Respir Rev
, vol.19
, pp. 237-241
-
-
Wells, A.U.1
-
70
-
-
80053557379
-
Bronchoalveolar lavage for the evaluation of interstitial lung disease: Is it clinically useful?
-
Meyer KC, Raghu G. Bronchoalveolar lavage for the evaluation of interstitial lung disease: is it clinically useful? Eur Respir J 2011; 38: 761-769.
-
(2011)
Eur Respir J
, vol.38
, pp. 761-769
-
-
Meyer, K.C.1
Raghu, G.2
-
71
-
-
66249145452
-
Significance of broncho-alveolar lavage for the diagnosis of idiopathic pulmonary fibrosis
-
Ohshimo S, Bonella F, Cui A, et al. Significance of broncho-alveolar lavage for the diagnosis of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2009; 179: 1043-1047.
-
(2009)
Am J Respir Crit Care Med
, vol.179
, pp. 1043-1047
-
-
Ohshimo, S.1
Bonella, F.2
Cui, A.3
-
72
-
-
0018830853
-
Pulmonary alveolar proteinosis: The diagnosis by segmental lavage
-
Martin RJ, Coalson JJ, Rogers RM, et al. Pulmonary alveolar proteinosis: the diagnosis by segmental lavage. Am Rev Respir Dis 1980; 121: 819-825.
-
(1980)
Am Rev Respir Dis
, vol.121
, pp. 819-825
-
-
Martin, R.J.1
Coalson, J.J.2
Rogers, R.M.3
-
73
-
-
0028118882
-
Establishing diagnosis of pulmonary malignant lymphoma by gene rearrangement analysis of lymphocytes in bronchoalveolar lavage fluid
-
Betsuyaku T, Munakata M, Yamaguchi E, et al. Establishing diagnosis of pulmonary malignant lymphoma by gene rearrangement analysis of lymphocytes in bronchoalveolar lavage fluid. Am J Respir Crit Care Med 1994; 149: 526-529.
-
(1994)
Am J Respir Crit Care Med
, vol.149
, pp. 526-529
-
-
Betsuyaku, T.1
Munakata, M.2
Yamaguchi, E.3
-
75
-
-
0032725125
-
The accuracy of the clinical diagnosis of new-onset idiopathic pulmonary fibrosis and other interstitial lung disease: A prospective study
-
Raghu G, Mageto YN, Lockhart D, et al. The accuracy of the clinical diagnosis of new-onset idiopathic pulmonary fibrosis and other interstitial lung disease: a prospective study. Chest 1999; 116: 1168-1174.
-
(1999)
Chest
, vol.116
, pp. 1168-1174
-
-
Raghu, G.1
Mageto, Y.N.2
Lockhart, D.3
-
76
-
-
79958245658
-
Towards a better diagnosis of idiopathic pulmonary fibrosis
-
Valeyre D. Towards a better diagnosis of idiopathic pulmonary fibrosis. Eur Respir Rev 2011; 20: 108-113.
-
(2011)
Eur Respir Rev
, vol.20
, pp. 108-113
-
-
Valeyre, D.1
-
77
-
-
51549101867
-
Interstitial lung disease guideline: The British Thoracic Society in collaboration with the Thoracic Society of Australia and New Zealand and the Irish Thoracic Society
-
Bradley B, Branley HM, Egan JJ, et al. Interstitial lung disease guideline: the British Thoracic Society in collaboration with the Thoracic Society of Australia and New Zealand and the Irish Thoracic Society. Thorax 2008; 63: Suppl. 5, v1-v58.
-
(2008)
Thorax
, vol.63
, Issue.SUPPL. 5
-
-
Bradley, B.1
Branley, H.M.2
Egan, J.J.3
-
78
-
-
77953077453
-
Clinical predictors of a diagnosis of idiopathic pulmonary fibrosis
-
Fell CD, Martinez FJ, Liu LX, et al. Clinical predictors of a diagnosis of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2010; 181: 832-837.
-
(2010)
Am J Respir Crit Care Med
, vol.181
, pp. 832-837
-
-
Fell, C.D.1
Martinez, F.J.2
Liu, L.X.3
-
79
-
-
77957967906
-
Lung disease
-
In: Albert RK, Spiro SG, Jett JR, eds., 3rd Edn. London, Mosby
-
Wells AU. Lung disease. In: Albert RK, Spiro SG, Jett JR, eds. Clinical Respiratory Medicine. 3rd Edn. London, Mosby, 2008; pp. 655-666.
-
(2008)
Clinical Respiratory Medicine
, pp. 655-666
-
-
Wells, A.U.1
-
80
-
-
44449152061
-
Interstitial lung disease in systemic sclerosis: A simple staging system
-
Goh NS, Desai SR, Veeraraghavan S, et al. Interstitial lung disease in systemic sclerosis: a simple staging system. Am J Respir Crit Care Med 2008; 177: 1248-1254.
-
(2008)
Am J Respir Crit Care Med
, vol.177
, pp. 1248-1254
-
-
Goh, N.S.1
Desai, S.R.2
Veeraraghavan, S.3
-
81
-
-
38349039634
-
Idiopathic pulmonary fibrosis: Outcome in relation to smoking status
-
Antoniou KM, Hansell DM, Rubens MB, et al. Idiopathic pulmonary fibrosis: outcome in relation to smoking status. Am J Respir Crit Care Med 2008; 177: 190-194.
-
(2008)
Am J Respir Crit Care Med
, vol.177
, pp. 190-194
-
-
Antoniou, K.M.1
Hansell, D.M.2
Rubens, M.B.3
-
82
-
-
26844449508
-
Combined pulmonary fibrosis and emphysema: A distinct underrecognised entity
-
Cottin V, Nunes H, Brillet PY, et al. Combined pulmonary fibrosis and emphysema: a distinct underrecognised entity. Eur Respir J 2005; 26: 586-593.
-
(2005)
Eur Respir J
, vol.26
, pp. 586-593
-
-
Cottin, V.1
Nunes, H.2
Brillet, P.Y.3
-
83
-
-
67650786507
-
Idiopathic pulmonary fibrosis and emphysema: Decreased survival associated with severe pulmonary arterial hypertension
-
Mejía M, Carrillo G, Rojas-Serrano J, et al. Idiopathic pulmonary fibrosis and emphysema: decreased survival associated with severe pulmonary arterial hypertension. Chest 2009; 136: 10-15.
-
(2009)
Chest
, vol.136
, pp. 10-15
-
-
Mejía, M.1
Carrillo, G.2
Rojas-Serrano, J.3
-
84
-
-
75149155845
-
Pulmonary hypertension in patients with combined pulmonary fibrosis and emphysema syndrome
-
Cottin V, Le Pavec J, Prévot G, et al. Pulmonary hypertension in patients with combined pulmonary fibrosis and emphysema syndrome. Eur Respir J 2010; 35: 105-111.
-
(2010)
Eur Respir J
, vol.35
, pp. 105-111
-
-
Cottin, V.1
le Pavec, J.2
Prévot, G.3
-
85
-
-
76149105846
-
Smoking-related lung diseases: A clinical perspective
-
Balbi B, Cottin V, Singh S, et al. Smoking-related lung diseases: a clinical perspective. Eur Respir J 2010; 35: 231-233.
-
(2010)
Eur Respir J
, vol.35
, pp. 231-233
-
-
Balbi, B.1
Cottin, V.2
Singh, S.3
-
86
-
-
78650783836
-
Combined pulmonary fibrosis and emphysema syndrome in connective tissue disease
-
Cottin V, Nunes H, Mouthon L, et al. Combined pulmonary fibrosis and emphysema syndrome in connective tissue disease. Arthritis Rheum 2011; 63: 295-304.
-
(2011)
Arthritis Rheum
, vol.63
, pp. 295-304
-
-
Cottin, V.1
Nunes, H.2
Mouthon, L.3
-
87
-
-
0032433225
-
Increased prevalence of gastroesophageal reflux in patients with idiopathic pulmonary fibrosis
-
Tobin RW, Pope CE 2nd, Pellegrini CA, et al. Increased prevalence of gastroesophageal reflux in patients with idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 1998; 158: 1804-1808.
-
(1998)
Am J Respir Crit Care Med
, vol.158
, pp. 1804-1808
-
-
Tobin, R.W.1
Pope, C.E.2
Pellegrini, C.A.3
-
88
-
-
30744455313
-
High prevalence of abnormal acid gastro-oesophageal reflux in idiopathic pulmonary fibrosis
-
Raghu G, Freudenberger TD, Yang S, et al. High prevalence of abnormal acid gastro-oesophageal reflux in idiopathic pulmonary fibrosis. Eur Respir J 2006; 27: 136-142.
-
(2006)
Eur Respir J
, vol.27
, pp. 136-142
-
-
Raghu, G.1
Freudenberger, T.D.2
Yang, S.3
-
89
-
-
79951950906
-
Progression of idiopathic pulmonary fibrosis: Lessons from asymmetrical disease
-
Tcherakian C, Cottin V, Brillet PY, et al. Progression of idiopathic pulmonary fibrosis: lessons from asymmetrical disease. Thorax 2011; 66: 226-231.
-
(2011)
Thorax
, vol.66
, pp. 226-231
-
-
Tcherakian, C.1
Cottin, V.2
Brillet, P.Y.3
-
90
-
-
79951947819
-
If it was good enough for Aristotle
-
Maher TM, Wells AU. If it was good enough for Aristotle. Thorax 2011; 66: 183-184.
-
(2011)
Thorax
, vol.66
, pp. 183-184
-
-
Maher, T.M.1
Wells, A.U.2
-
91
-
-
30144438578
-
The impact of pulmonary hypertension on survival in patients with idiopathic pulmonary fibrosis
-
Nadrous HF, Pellikka PA, Krowka MJ, et al. The impact of pulmonary hypertension on survival in patients with idiopathic pulmonary fibrosis. Chest 2005; 128: Suppl. 6, 616S-617S.
-
(2005)
Chest
, vol.128
, Issue.SUPPL. 6
-
-
Nadrous, H.F.1
Pellikka, P.A.2
Krowka, M.J.3
-
92
-
-
33947370516
-
Significance of pulmonary arterial pressure and diffusion capacity of the lung as prog-nosticator in patients with idiopathic pulmonary fibrosis
-
Hamada K, Nagai S, Tanaka S, et al. Significance of pulmonary arterial pressure and diffusion capacity of the lung as prog-nosticator in patients with idiopathic pulmonary fibrosis. Chest 2007; 131: 650-656.
-
(2007)
Chest
, vol.131
, pp. 650-656
-
-
Hamada, K.1
Nagai, S.2
Tanaka, S.3
-
93
-
-
33645118315
-
Prevalence and outcomes of pulmonary arterial hypertension in advanced idiopathic pulmonary fibrosis
-
Lettieri CJ, Nathan SD, Barnett SD, et al. Prevalence and outcomes of pulmonary arterial hypertension in advanced idiopathic pulmonary fibrosis. Chest 2006; 129: 746-752.
-
(2006)
Chest
, vol.129
, pp. 746-752
-
-
Lettieri, C.J.1
Nathan, S.D.2
Barnett, S.D.3
-
94
-
-
27144547143
-
Pulmonary hypertension in patients with idiopathic pulmonary fibrosis
-
Nadrous HF, Pellikka PA, Krowka MJ, et al. Pulmonary hypertension in patients with idiopathic pulmonary fibrosis. Chest 2005; 128: 2393-2399.
-
(2005)
Chest
, vol.128
, pp. 2393-2399
-
-
Nadrous, H.F.1
Pellikka, P.A.2
Krowka, M.J.3
-
95
-
-
38449102031
-
Pulmonary hypertension in patients with pulmonary fibrosis awaiting lung transplant
-
Shorr AF, Wainright JL, Cors CS, et al. Pulmonary hypertension in patients with pulmonary fibrosis awaiting lung transplant. Eur Respir J 2007; 30: 715-721.
-
(2007)
Eur Respir J
, vol.30
, pp. 715-721
-
-
Shorr, A.F.1
Wainright, J.L.2
Cors, C.S.3
-
96
-
-
32944476373
-
Noninvasive estimation of clinically asymptomatic pulmonary hypertension in idiopathic pulmonary fibrosis
-
Agarwal R, Gupta D, Verma JS, et al. Noninvasive estimation of clinically asymptomatic pulmonary hypertension in idiopathic pulmonary fibrosis. Indian J Chest Dis Allied Sci 2005; 47: 267-271.
-
(2005)
Indian J Chest Dis Allied Sci
, vol.47
, pp. 267-271
-
-
Agarwal, R.1
Gupta, D.2
Verma, J.S.3
-
97
-
-
53149152248
-
Serial development of pulmonary hypertension in patients with idiopathic pulmonary fibrosis
-
Nathan SD, Shlobin OA, Ahmad S, et al. Serial development of pulmonary hypertension in patients with idiopathic pulmonary fibrosis. Respiration 2008; 76: 288-294.
-
(2008)
Respiration
, vol.76
, pp. 288-294
-
-
Nathan, S.D.1
Shlobin, O.A.2
Ahmad, S.3
-
98
-
-
18744381053
-
Pulmonary hypertension in advanced sarcoidosis: Epidemiology and clinical characteristics
-
Shorr AF, Helman DL, Davies DB, et al. Pulmonary hypertension in advanced sarcoidosis: epidemiology and clinical characteristics. Eur Respir J 2005; 25: 783-788.
-
(2005)
Eur Respir J
, vol.25
, pp. 783-788
-
-
Shorr, A.F.1
Helman, D.L.2
Davies, D.B.3
-
99
-
-
70349673627
-
Pulmonary vascular resistance predicts early mortality in patients with diffuse fibrotic lung disease and suspected pulmonary hypertension
-
Corte TJ, Wort SJ, Gatzoulis MA, et al. Pulmonary vascular resistance predicts early mortality in patients with diffuse fibrotic lung disease and suspected pulmonary hypertension. Thorax 2009; 64: 883-888.
-
(2009)
Thorax
, vol.64
, pp. 883-888
-
-
Corte, T.J.1
Wort, S.J.2
Gatzoulis, M.A.3
-
100
-
-
58249092608
-
Echocardiography and brain natriuretic peptide as prognostic indicators in idiopathic pulmonary fibrosis
-
Song JW, Song JK, Kim DS. Echocardiography and brain natriuretic peptide as prognostic indicators in idiopathic pulmonary fibrosis. Respir Med 2009; 103: 180-186.
-
(2009)
Respir Med
, vol.103
, pp. 180-186
-
-
Song, J.W.1
Song, J.K.2
Kim, D.S.3
-
101
-
-
77957852320
-
Elevated brain natriuretic peptide predicts mortality in interstitial lung disease
-
Corte TJ, Wort SJ, Gatzoulis MA, et al. Elevated brain natriuretic peptide predicts mortality in interstitial lung disease. Eur Respir J 2010; 36: 819-825.
-
(2010)
Eur Respir J
, vol.36
, pp. 819-825
-
-
Corte, T.J.1
Wort, S.J.2
Gatzoulis, M.A.3
-
102
-
-
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: 164-168.
-
(2006)
Respirology
, vol.11
, pp. 164-168
-
-
Yokoyama, A.1
Kondo, K.2
Nakajima, M.3
-
103
-
-
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: 439-446.
-
(2002)
Eur Respir J
, vol.19
, pp. 439-446
-
-
Greene, K.E.1
King, T.E.2
Kuroki, Y.3
-
104
-
-
0027418167
-
Elevated levels of lung surfactant protein A in sera from patients with idiopathic pulmonary fibrosis and pulmonary alveolar proteinosis
-
Kuroki Y, Tsutahara S, Shijubo N, et al. Elevated levels of lung surfactant protein A in sera from patients with idiopathic pulmonary fibrosis and pulmonary alveolar proteinosis. Am Rev Respir Dis 1993; 147: 723-729.
-
(1993)
Am Rev Respir Dis
, vol.147
, pp. 723-729
-
-
Kuroki, Y.1
Tsutahara, S.2
Shijubo, N.3
-
105
-
-
0037260159
-
High serum concentrations of surfactant protein A in usual interstitial pneumonia compared with non-specific interstitial pneumonia
-
Ishii H, Mukae H, Kadota J, et al. High serum concentrations of surfactant protein A in usual interstitial pneumonia compared with non-specific interstitial pneumonia. Thorax 2003; 58: 52-57.
-
(2003)
Thorax
, vol.58
, pp. 52-57
-
-
Ishii, H.1
Mukae, H.2
Kadota, J.3
-
106
-
-
0037251554
-
Prognostic value of surfactant proteins A and D in patients with acute lung injury
-
Cheng IW, Ware LB, Greene KE, et al. Prognostic value of surfactant proteins A and D in patients with acute lung injury. Crit Care Med 2003; 31: 20-27.
-
(2003)
Crit Care Med
, vol.31
, pp. 20-27
-
-
Cheng, I.W.1
Ware, L.B.2
Greene, K.E.3
-
107
-
-
63849228099
-
Serum surfactant protein-A is a strong predictor of early mortality in idiopathic pulmonary fibrosis
-
Kinder BW, Brown KK, McCormack FX, et al. Serum surfactant protein-A is a strong predictor of early mortality in idiopathic pulmonary fibrosis. Chest 2009; 135: 1557-1563.
-
(2009)
Chest
, vol.135
, pp. 1557-1563
-
-
Kinder, B.W.1
Brown, K.K.2
McCormack, F.X.3
-
108
-
-
58849094483
-
MMP expression and abnormal lung permeability are important determinants of outcome in IPF
-
McKeown S, Richter AG, O'Kane C, et al. MMP expression and abnormal lung permeability are important determinants of outcome in IPF. Eur Respir J 2009; 33: 77-84.
-
(2009)
Eur Respir J
, vol.33
, pp. 77-84
-
-
McKeown, S.1
Richter, A.G.2
O'Kane, C.3
-
109
-
-
65249160219
-
Serum CC-chemokine ligand 18 concentration predicts outcome in idiopathic pulmonary fibrosis
-
Prasse A, Probst C, Bargagli E, et al. Serum CC-chemokine ligand 18 concentration predicts outcome in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2009; 179: 717-723.
-
(2009)
Am J Respir Crit Care Med
, vol.179
, pp. 717-723
-
-
Prasse, A.1
Probst, C.2
Bargagli, E.3
-
110
-
-
33645845729
-
Exhaled markers of oxidative stress in idiopathic pulmonary fibrosis
-
Psathakis K, Mermigkis D, Papatheodorou G, et al. Exhaled markers of oxidative stress in idiopathic pulmonary fibrosis. Eur J Clin Invest 2006; 36: 362-367.
-
(2006)
Eur J Clin Invest
, vol.36
, pp. 362-367
-
-
Psathakis, K.1
Mermigkis, D.2
Papatheodorou, G.3
-
111
-
-
38349060783
-
Baseline BAL neutrophilia predicts early mortality in idiopathic pulmonary fibrosis
-
Kinder BW, Brown KK, Schwarz MI, et al. Baseline BAL neutrophilia predicts early mortality in idiopathic pulmonary fibrosis. Chest 2008; 133: 226-232.
-
(2008)
Chest
, vol.133
, pp. 226-232
-
-
Kinder, B.W.1
Brown, K.K.2
Schwarz, M.I.3
-
112
-
-
10744222693
-
BAL findings in idiopathic nonspecific interstitial pneumonia and usual interstitial pneumonia
-
Veeraraghavan S, Latsi PI, Wells AU, et al. BAL findings in idiopathic nonspecific interstitial pneumonia and usual interstitial pneumonia. Eur Respir J 2003; 22: 239-24.4.
-
(2003)
Eur Respir J
, vol.22
, pp. 239-244
-
-
Veeraraghavan, S.1
Latsi, P.I.2
Wells, A.U.3
-
113
-
-
0027953965
-
Fibrosing alveolitis in systemic sclerosis. Bronchoalveolar lavage findings in relation to computed tomographic appearance
-
Wells AU, Hansell DM, Rubens MB, et al. Fibrosing alveolitis in systemic sclerosis. Bronchoalveolar lavage findings in relation to computed tomographic appearance. Am J Respir Crit Care Med 1994; 150: 462-468.
-
(1994)
Am J Respir Crit Care Med
, vol.150
, pp. 462-468
-
-
Wells, A.U.1
Hansell, D.M.2
Rubens, M.B.3
-
114
-
-
34447520311
-
Bronchoalveolar lavage cellular profiles in patients with systemic sclerosis-associated interstitial lung disease are not predictive of disease progression
-
Goh NS, Veeraraghavan S, Desai SR, et al. Bronchoalveolar lavage cellular profiles in patients with systemic sclerosis-associated interstitial lung disease are not predictive of disease progression. Arthritis Rheum 2007; 56: 2005-2012.
-
(2007)
Arthritis Rheum
, vol.56
, pp. 2005-2012
-
-
Goh, N.S.1
Veeraraghavan, S.2
Desai, S.R.3
-
115
-
-
79955674250
-
Periostin, a matrix protein, is a novel biomarker for idiopathic interstitial pneumonias
-
Okamoto M, Hoshino T, Kitasato Y, et al. Periostin, a matrix protein, is a novel biomarker for idiopathic interstitial pneumonias. Eur Respir J 2011; 37: 1119-1127.
-
(2011)
Eur Respir J
, vol.37
, pp. 1119-1127
-
-
Okamoto, M.1
Hoshino, T.2
Kitasato, Y.3
-
116
-
-
77951160564
-
Pirfenidone in idiopathic pulmonary fibrosis
-
Taniguchi H, Ebina M, Kondoh Y, et al. Pirfenidone in idiopathic pulmonary fibrosis. Eur Respir J 2010; 35: 821-829.
-
(2010)
Eur Respir J
, vol.35
, pp. 821-829
-
-
Taniguchi, H.1
Ebina, M.2
Kondoh, Y.3
-
117
-
-
80052591490
-
A first step against idiopathic pulmonary fibrosis
-
Crestani B. A first step against idiopathic pulmonary fibrosis. Eur Respir Rev 2011; 20: 130-131.
-
(2011)
Eur Respir Rev
, vol.20
, pp. 130-131
-
-
Crestani, B.1
-
118
-
-
80052536198
-
Emerging potential treatments: New hope for idiopathic pulmonary fibrosis patients?
-
Costabel U. Emerging potential treatments: new hope for idiopathic pulmonary fibrosis patients? Eur Respir Rev 2011; 20: 201-207.
-
(2011)
Eur Respir Rev
, vol.20
, pp. 201-207
-
-
Costabel, U.1
-
119
-
-
80052533421
-
Idiopathic pulmonary fibrosis: Present understanding and future options
-
du Bois RM. Idiopathic pulmonary fibrosis: present understanding and future options. Eur Respir Rev 2011; 20: 132-133.
-
(2011)
Eur Respir Rev
, vol.20
, pp. 132-133
-
-
du Bois, R.M.1
-
120
-
-
38849178850
-
Idiopathic pulmonary fibrosis: Multiple causes and multiple mechanisms?
-
Maher TM, Wells AU, Laurent GJ. Idiopathic pulmonary fibrosis: multiple causes and multiple mechanisms? Eur Respir J 2007; 30: 835-839.
-
(2007)
Eur Respir J
, vol.30
, pp. 835-839
-
-
Maher, T.M.1
Wells, A.U.2
Laurent, G.J.3
|