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Volumn 20, Issue 120, 2011, Pages 108-113

Towards a better diagnosis of idiopathic pulmonary fibrosis

Author keywords

Diagnosis; Idiopathic pulmonary fibrosis

Indexed keywords

CD28 ANTIGEN; GLYCOPROTEIN; INTERLEUKIN 8; INTERSTITIAL COLLAGENASE; KREBS VON LUNGEN FACTOR 6; MATRILYSIN; SURFACTANT PROTEIN A; SURFACTANT PROTEIN D; UNCLASSIFIED DRUG; VASCULOTROPIN;

EID: 79958245658     PISSN: 09059180     EISSN: None     Source Type: Journal    
DOI: 10.1183/09059180.00001611     Document Type: Review
Times cited : (22)

References (58)
  • 1
    • 0037080547 scopus 로고    scopus 로고
    • American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias
    • American Thoracic Society, European Respiratory Society
    • American Thoracic Society, European Respiratory Society. American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. Am J Respir Crit Care Med 2002; 165: 277-304.
    • (2002) Am J Respir Crit Care Med , vol.165 , pp. 277-304
  • 2
    • 33749444308 scopus 로고    scopus 로고
    • Incidence and prevalence of idiopathic pulmonary fibrosis
    • Raghu G, Weycker D, Edelsberg J, et al. Incidence and prevalence of idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2006; 174: 810-816.
    • (2006) Am J Respir Crit Care Med , vol.174 , pp. 810-816
    • Raghu, G.1    Weycker, D.2    Edelsberg, J.3
  • 3
    • 0034011982 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis: Diagnosis and treatment. International consensus statement. American Thoracic Society (ATS), and the European Respiratory Society (ERS)
    • American Thoracic Society
    • American Thoracic Society. Idiopathic pulmonary fibrosis: diagnosis and treatment. International consensus statement. American Thoracic Society (ATS), and the European Respiratory Society (ERS). Am J Respir Crit Care Med 2000; 161: 646-664.
    • (2000) Am J Respir Crit Care Med , vol.161 , pp. 646-664
  • 5
    • 33744914050 scopus 로고    scopus 로고
    • 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
  • 6
    • 28044447391 scopus 로고    scopus 로고
    • Pathogenesis and natural history of usual interstitial pneumonia: The whole story or the last chapter of a long novel
    • Strieter RM. Pathogenesis and natural history of usual interstitial pneumonia: the whole story or the last chapter of a long novel. Chest 2005; 128: Suppl. 1, 526S-532S.
    • (2005) Chest , vol.128 , Issue.SUPPL. 1
    • Strieter, R.M.1
  • 7
    • 80053644482 scopus 로고    scopus 로고
    • The TrkB/NT4 signaling axis is perturbed in clinical and experimental pulmonary fibrosis
    • [Epub ahead of print DOI:10.1165/rcmb.2010-0195OC]
    • Avcuoglu S, Wygrecka M, Marsh LM, et al. The TrkB/NT4 signaling axis is perturbed in clinical and experimental pulmonary fibrosis. Am J Respir Cell Mol Biol 2011; [Epub ahead of print DOI:10.1165/rcmb.2010-0195OC].
    • (2011) Am J Respir Cell Mol Biol
    • Avcuoglu, S.1    Wygrecka, M.2    Marsh, L.M.3
  • 8
    • 24344473068 scopus 로고    scopus 로고
    • Back to the future: Historical perspective on the pathogenesis of idiopathic pulmonary fibrosis
    • Noble PW, Homer RJ. Back to the future: historical perspective on the pathogenesis of idiopathic pulmonary fibrosis. Am J Respir Cell Mol Biol 2005; 33: 113-120.
    • (2005) Am J Respir Cell Mol Biol , vol.33 , pp. 113-120
    • Noble, P.W.1    Homer, R.J.2
  • 10
    • 79958283372 scopus 로고    scopus 로고
    • The development of evidence-based guidelines of the ATS, ERS, JRS and ALAT Joint Task Force for the management of IPF: New diagnostic criteria, natural course and approach to the diagnosis of IPF
    • New Orleans, USA. B82
    • Raghu G. The development of evidence-based guidelines of the ATS, ERS, JRS and ALAT Joint Task Force for the management of IPF: new diagnostic criteria, natural course and approach to the diagnosis of IPF. 2010 American Thoracic Society Congress, New Orleans, USA. B82.
    • 2010 American Thoracic Society Congress
    • Raghu, G.1
  • 11
    • 20544443765 scopus 로고    scopus 로고
    • 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: 963-967.
    • (2005) Ann Intern Med , vol.142 , pp. 963-967
    • Martinez, F.J.1    Safrin, S.2    Weycker, D.3
  • 12
    • 31144455105 scopus 로고    scopus 로고
    • Interstitial lung disease: Effects of thin-section CT on clinical decision making
    • Aziz ZA, Wells AU, Bateman ED, et al. Interstitial lung disease: effects of thin-section CT on clinical decision making. Radiology 2006; 238: 725-733.
    • (2006) Radiology , vol.238 , pp. 725-733
    • Aziz, Z.A.1    Wells, A.U.2    Bateman, E.D.3
  • 13
    • 70049115332 scopus 로고    scopus 로고
    • Diagnosing fibrotic lung disease: When is high-resolution computed tomography sufficient to make a diagnosis of idiopathic pulmonary fibrosis?
    • Schmidt SL, Sundaram B, Flaherty KR. Diagnosing fibrotic lung disease: when is high-resolution computed tomography sufficient to make a diagnosis of idiopathic pulmonary fibrosis? Respirology 2009; 14: 934-939.
    • (2009) Respirology , vol.14 , pp. 934-939
    • Schmidt, S.L.1    Sundaram, B.2    Flaherty, K.R.3
  • 14
    • 39849111240 scopus 로고    scopus 로고
    • Computed tomography findings in pathological usual interstitial pneumonia: Relationship to survival
    • Sumikawa H, Johkoh T, Colby TV, et al. Computed tomography findings in pathological usual interstitial pneumonia: relationship to survival. Am J Respir Crit Care Med 2008; 177: 433-439.
    • (2008) Am J Respir Crit Care Med , vol.177 , pp. 433-439
    • Sumikawa, H.1    Johkoh, T.2    Colby, T.V.3
  • 15
    • 34250340389 scopus 로고    scopus 로고
    • Challenges in pulmonary fibrosis. 1: Use of high resolution CT scanning of the lung for the evaluation of patients with idiopathic interstitial pneumonias
    • Gotway MB, Freemer MM, King TE Jr. Challenges in pulmonary fibrosis. 1: Use of high resolution CT scanning of the lung for the evaluation of patients with idiopathic interstitial pneumonias. Thorax 2007; 62: 546-553.
    • (2007) Thorax , vol.62 , pp. 546-553
    • Gotway, M.B.1    Freemer, M.M.2    King Jr., T.E.3
  • 16
    • 34548031633 scopus 로고    scopus 로고
    • Recent advances in idiopathic pulmonary fibrosis
    • Noth I, Martinez FJ. Recent advances in idiopathic pulmonary fibrosis. Chest 2007; 132: 637-650.
    • (2007) Chest , vol.132 , pp. 637-650
    • Noth, I.1    Martinez, F.J.2
  • 17
    • 5144222998 scopus 로고    scopus 로고
    • Idiopathic interstitial pneumonia: What is the effect of a multidisciplinary approach to diagnosis?
    • Flaherty KR, King TE Jr, 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 Jr., T.E.2    Raghu, G.3
  • 18
    • 34248372493 scopus 로고    scopus 로고
    • Idiopathic interstitial pneumonia: Do community and academic physicians agree on diagnosis?
    • Flaherty KR, Andrei AC, King TE Jr, et al. Idiopathic interstitial pneumonia: do community and academic physicians agree on diagnosis? Am J Respir Crit Care Med 2007; 175: 1054-1060.
    • (2007) Am J Respir Crit Care Med , vol.175 , pp. 1054-1060
    • Flaherty, K.R.1    Andrei, A.C.2    King Jr., T.E.3
  • 19
    • 0034074826 scopus 로고    scopus 로고
    • Sarcoidosis with pulmonary fibrosis: CT patterns and correlation with pulmonary function
    • Abehsera M, Valeyre D, Grenier P, et al. Sarcoidosis with pulmonary fibrosis: CT patterns and correlation with pulmonary function. AJR Am J Roentgenol 2000; 174: 1751-1757.
    • (2000) AJR Am J Roentgenol , vol.174 , pp. 1751-1757
    • Abehsera, M.1    Valeyre, D.2    Grenier, P.3
  • 20
    • 22644439391 scopus 로고    scopus 로고
    • Pulmonary sarcoidosis mimicking cryptogenic fibrosing alveolitis on CT
    • Padley SP, Padhani AR, Nicholson A, et al. Pulmonary sarcoidosis mimicking cryptogenic fibrosing alveolitis on CT. Clin Radiol 1996; 51: 807-810.
    • (1996) Clin Radiol , vol.51 , pp. 807-810
    • Padley, S.P.1    Padhani, A.R.2    Nicholson, A.3
  • 21
    • 77951192926 scopus 로고    scopus 로고
    • Chronic interstitial pneumonitis in end-stage sarcoidosis
    • Shigemitsu H, Oblad JM, Sharma OP, et al. Chronic interstitial pneumonitis in end-stage sarcoidosis. Eur Respir J 2010; 35: 695-697.
    • (2010) Eur Respir J , vol.35 , pp. 695-697
    • Shigemitsu, H.1    Oblad, J.M.2    Sharma, O.P.3
  • 22
    • 42949087510 scopus 로고    scopus 로고
    • Multidisciplinary interobserver agreement in the diagnosis of idiopathic pulmonary fibrosis
    • Thomeer M, Demedts M, Behr J, et al. Multidisciplinary interobserver agreement in the diagnosis of idiopathic pulmonary fibrosis. Eur Respir J 2008; 31: 585-591.
    • (2008) Eur Respir J , vol.31 , pp. 585-591
    • Thomeer, M.1    Demedts, M.2    Behr, J.3
  • 23
    • 77953077453 scopus 로고    scopus 로고
    • 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
  • 24
    • 28144437469 scopus 로고    scopus 로고
    • Multi-detector row CT and postprocessing techniques in the assessment of diffuse lung disease
    • Beigelman-Aubry C, Hill C, Guibal A, et al. Multi-detector row CT and postprocessing techniques in the assessment of diffuse lung disease. Radiographics 2005; 25: 1639-1652.
    • (2005) Radiographics , vol.25 , pp. 1639-1652
    • Beigelman-Aubry, C.1    Hill, C.2    Guibal, A.3
  • 25
    • 56349090868 scopus 로고    scopus 로고
    • Automated classification of normal and pathologic pulmonary tissue by topological texture features extracted from multi-detector CT in 3D
    • Boehm HF, Fink C, Attenberger U, et al. Automated classification of normal and pathologic pulmonary tissue by topological texture features extracted from multi-detector CT in 3D. Eur Radiol 2008; 18: 2745-2755.
    • (2008) Eur Radiol , vol.18 , pp. 2745-2755
    • Boehm, H.F.1    Fink, C.2    Attenberger, U.3
  • 26
    • 78449269444 scopus 로고    scopus 로고
    • 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
  • 27
    • 77953187384 scopus 로고    scopus 로고
    • Update on diffuse parenchymal lung disease
    • Harari S, Caminati A. Update on diffuse parenchymal lung disease. Eur Respir Rev 2010; 19: 97-108.
    • (2010) Eur Respir Rev , vol.19 , pp. 97-108
    • Harari, S.1    Caminati, A.2
  • 28
    • 38349060783 scopus 로고    scopus 로고
    • 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
  • 29
    • 0041374155 scopus 로고    scopus 로고
    • Fibrotic idiopathic interstitial pneumonia: The prognostic value of longitudinal functional trends
    • 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: 531-537.
    • (2003) Am J Respir Crit Care Med , vol.168 , pp. 531-537
    • Latsi, P.I.1    du Bois, R.M.2    Nicholson, A.G.3
  • 30
    • 33749434364 scopus 로고    scopus 로고
    • Idiopathic pulmonary fibrosis: Prognostic value of changes in physiology and sixminute- walk test
    • Flaherty KR, Andrei AC, Murray S, et al. Idiopathic pulmonary fibrosis: prognostic value of changes in physiology and sixminute- walk test. Am J Respir Crit Care Med 2006; 174: 803-809.
    • (2006) Am J Respir Crit Care Med , vol.174 , pp. 803-809
    • Flaherty, K.R.1    Andrei, A.C.2    Murray, S.3
  • 31
    • 0041874992 scopus 로고    scopus 로고
    • 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: 538-542.
    • (2003) Am J Respir Crit Care Med , vol.168 , pp. 538-542
    • Collard, H.R.1    King Jr., T.E.2    Bartelson, B.B.3
  • 32
    • 20144381640 scopus 로고    scopus 로고
    • 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: 639-644.
    • (2005) Am J Respir Crit Care Med , vol.171 , pp. 639-644
    • Jegal, Y.1    Kim, D.S.2    Shim, T.S.3
  • 33
    • 0029091234 scopus 로고
    • Changes in pulmonary function test results after 1 year of therapy as predictors of survival in patients with idiopathic pulmonary fibrosis
    • Hanson D, Winterbauer RH, Kirtland SH, et al. Changes in pulmonary function test results after 1 year of therapy as predictors of survival in patients with idiopathic pulmonary fibrosis. Chest 1995; 108: 305-310.
    • (1995) Chest , vol.108 , pp. 305-310
    • Hanson, D.1    Winterbauer, R.H.2    Kirtland, S.H.3
  • 34
    • 77951170794 scopus 로고    scopus 로고
    • 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: 830-836.
    • (2010) Eur Respir J , vol.35 , pp. 830-836
    • Zappala, C.J.1    Latsi, P.I.2    Nicholson, A.G.3
  • 35
    • 0024332651 scopus 로고
    • New serum indicator of interstitial pneumonitis activity. Sialylated carbohydrate antigen KL-6
    • Kohno N, Kyoizumi S, Awaya Y, et al. New serum indicator of interstitial pneumonitis activity. Sialylated carbohydrate antigen KL-6. Chest 1989; 96: 68-73.
    • (1989) Chest , vol.96 , pp. 68-73
    • Kohno, N.1    Kyoizumi, S.2    Awaya, Y.3
  • 36
    • 33750018921 scopus 로고    scopus 로고
    • Increased levels of KL-6 and subsequent mortality in patients with interstitial lung diseases
    • Satoh H, Kurishima K, Ishikawa H, et al. Increased levels of KL-6 and subsequent mortality in patients with interstitial lung diseases. J Intern Med 2006; 260: 429-434.
    • (2006) J Intern Med , vol.260 , pp. 429-434
    • Satoh, H.1    Kurishima, K.2    Ishikawa, H.3
  • 37
    • 33644828168 scopus 로고    scopus 로고
    • 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
  • 38
    • 0029111616 scopus 로고
    • Serum surfactant protein-A levels in patients with acute cardiogenic pulmonary oedema and adult respiratory distress syndrome
    • Doyle IR, Nicholas TE, Bersten AD. Serum surfactant protein-A levels in patients with acute cardiogenic pulmonary oedema and adult respiratory distress syndrome. Am J Respir Crit Care Med 1995; 152: 307-317.
    • (1995) Am J Respir Crit Care Med , vol.152 , pp. 307-317
    • Doyle, I.R.1    Nicholas, T.E.2    Bersten, A.D.3
  • 39
    • 0036196542 scopus 로고    scopus 로고
    • Serum surfactant proteins-A and -D as biomarkers in idiopathic pulmonary fibrosis
    • Greene KE, King TE Jr, 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 Jr., T.E.2    Kuroki, Y.3
  • 40
    • 0031795795 scopus 로고    scopus 로고
    • Surfactant proteins A and D: Disease markers
    • Kuroki Y, Takahashi H, Chiba H, et al. Surfactant proteins A and D: disease markers. Biochim Biophys Acta 1998; 1408: 334-345.
    • (1998) Biochim Biophys Acta , vol.1408 , pp. 334-345
    • Kuroki, Y.1    Takahashi, H.2    Chiba, H.3
  • 41
    • 0027418167 scopus 로고
    • 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
  • 42
    • 0037260159 scopus 로고    scopus 로고
    • 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
  • 43
    • 0037251554 scopus 로고    scopus 로고
    • 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
  • 44
    • 63849228099 scopus 로고    scopus 로고
    • 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
  • 45
    • 77952489797 scopus 로고    scopus 로고
    • CD28 down-regulation on circulating CD4 T-cells is associated with poor prognoses of patients with idiopathic pulmonary fibrosis
    • Gilani SR, Vuga LJ, Lindell KO, et al. CD28 down-regulation on circulating CD4 T-cells is associated with poor prognoses of patients with idiopathic pulmonary fibrosis. PLoS One 2010; 5: e8959.
    • (2010) PLoS One , vol.5
    • Gilani, S.R.1    Vuga, L.J.2    Lindell, K.O.3
  • 46
    • 33845639241 scopus 로고    scopus 로고
    • Circulating peripheral blood fibrocytes in human fibrotic interstitial lung disease
    • Mehrad B, Burdick MD, Zisman DA, et al. Circulating peripheral blood fibrocytes in human fibrotic interstitial lung disease. Biochem Biophys Res Commun 2007; 353: 104-108.
    • (2007) Biochem Biophys Res Commun , vol.353 , pp. 104-108
    • Mehrad, B.1    Burdick, M.D.2    Zisman, D.A.3
  • 47
    • 35748946038 scopus 로고    scopus 로고
    • Reduction of bleomycin-induced pulmonary fibrosis by serum amyloid P
    • Pilling D, Roife D, Wang M, et al. Reduction of bleomycin-induced pulmonary fibrosis by serum amyloid P. J Immunol 2007; 179: 4035-4044.
    • (2007) J Immunol , vol.179 , pp. 4035-4044
    • Pilling, D.1    Roife, D.2    Wang, M.3
  • 48
    • 65249098301 scopus 로고    scopus 로고
    • Circulating fibrocytes are an indicator of poor prognosis in idiopathic pulmonary fibrosis
    • Moeller A, Gilpin SE, Ask K, et al. Circulating fibrocytes are an indicator of poor prognosis in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2009; 179: 588-594.
    • (2009) Am J Respir Crit Care Med , vol.179 , pp. 588-594
    • Moeller, A.1    Gilpin, S.E.2    Ask, K.3
  • 49
    • 2542481862 scopus 로고    scopus 로고
    • Heterogeneous increase in CD34-positive alveolar capillaries in idiopathic pulmonary fibrosis
    • Ebina M, Shimizukawa M, Shibata N, et al. Heterogeneous increase in CD34-positive alveolar capillaries in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2004; 169: 1203-1208.
    • (2004) Am J Respir Crit Care Med , vol.169 , pp. 1203-1208
    • Ebina, M.1    Shimizukawa, M.2    Shibata, N.3
  • 50
    • 3142521656 scopus 로고    scopus 로고
    • Angiogenic cytokines in patients with idiopathic interstitial pneumonia
    • Simler NR, Brenchley PE, Horrocks AW, et al. Angiogenic cytokines in patients with idiopathic interstitial pneumonia. Thorax 2004; 59: 581-585.
    • (2004) Thorax , vol.59 , pp. 581-585
    • Simler, N.R.1    Brenchley, P.E.2    Horrocks, A.W.3
  • 51
    • 0036848469 scopus 로고    scopus 로고
    • Matrix metalloproteinases and tissue inhibitor of metalloproteinase-1 in sarcoidosis and IPF
    • Henry MT, McMahon K, Mackarel AJ, et al. Matrix metalloproteinases and tissue inhibitor of metalloproteinase-1 in sarcoidosis and IPF. Eur Respir J 2002; 20: 1220-1227.
    • (2002) Eur Respir J , vol.20 , pp. 1220-1227
    • Henry, M.T.1    McMahon, K.2    McKarel, A.J.3
  • 52
    • 0033679330 scopus 로고    scopus 로고
    • Characteristic elevation of matrix metalloproteinase activity in idiopathic interstitial pneumonias
    • Suga M, Iyonaga K, Okamoto T, et al. Characteristic elevation of matrix metalloproteinase activity in idiopathic interstitial pneumonias. Am J Respir Crit Care Med 2000; 162: 1949-1956.
    • (2000) Am J Respir Crit Care Med , vol.162 , pp. 1949-1956
    • Suga, M.1    Iyonaga, K.2    Okamoto, T.3
  • 53
    • 43649106124 scopus 로고    scopus 로고
    • Is metalloproteinase-7 specific for idiopathic pulmonary fibrosis?
    • Huh JW, Kim DS, Oh YM, et al. Is metalloproteinase-7 specific for idiopathic pulmonary fibrosis? Chest 2008; 133: 1101-1106.
    • (2008) Chest , vol.133 , pp. 1101-1106
    • Huh, J.W.1    Kim, D.S.2    Oh, Y.M.3
  • 54
    • 31944436620 scopus 로고    scopus 로고
    • Gene expression profiles distinguish idiopathic pulmonary fibrosis from hypersensitivity pneumonitis
    • Selman M, Pardo A, Barrera L, et al. Gene expression profiles distinguish idiopathic pulmonary fibrosis from hypersensitivity pneumonitis. Am J Respir Crit Care Med 2006; 173: 188-198.
    • (2006) Am J Respir Crit Care Med , vol.173 , pp. 188-198
    • Selman, M.1    Pardo, A.2    Barrera, L.3
  • 55
    • 43249084804 scopus 로고    scopus 로고
    • 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
    • Rosas, I.O.1    Richards, T.J.2    Konishi, K.3
  • 56
    • 77955092333 scopus 로고    scopus 로고
    • Oxidative stress, extracellular matrix targets, and idiopathic pulmonary fibrosis
    • Kliment CR, Oury TD. Oxidative stress, extracellular matrix targets, and idiopathic pulmonary fibrosis. Free Radic Biol Med 2010; 49: 707-717.
    • (2010) Free Radic Biol Med , vol.49 , pp. 707-717
    • Kliment, C.R.1    Oury, T.D.2
  • 57
    • 38049079133 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.