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Items: 1 to 20 of 126

1.

Detection of alveolar fibrocytes in idiopathic pulmonary fibrosis and systemic sclerosis.

Borie R, Quesnel C, Phin S, Debray MP, Marchal-Somme J, Tiev K, Bonay M, Fabre A, Soler P, Dehoux M, Crestani B.

PLoS One. 2013;8(1):e53736. doi: 10.1371/journal.pone.0053736. Epub 2013 Jan 16.

2.

BAL cytokine profile in different interstitial lung diseases: a focus on systemic sclerosis.

Meloni F, Caporali R, Marone Bianco A, Paschetto E, Morosini M, Fietta AM, Patrizio V, Bobbio-Pallavicini F, Pozzi E, Montecucco C.

Sarcoidosis Vasc Diffuse Lung Dis. 2004 Jun;21(2):111-8.

PMID:
15281432
3.

Role of inflammation in the lung disease of systemic sclerosis: comparison with idiopathic pulmonary fibrosis.

Owens GR, Paradis IL, Gryzan S, Medsger TA Jr, Follansbee WP, Klein HA, Dauber JH.

J Lab Clin Med. 1986 Mar;107(3):253-60.

PMID:
3950467
4.

Fibrocytes are a potential source of lung fibroblasts in idiopathic pulmonary fibrosis.

Andersson-Sjöland A, de Alba CG, Nihlberg K, Becerril C, Ramírez R, Pardo A, Westergren-Thorsson G, Selman M.

Int J Biochem Cell Biol. 2008;40(10):2129-40. doi: 10.1016/j.biocel.2008.02.012. Epub 2008 Mar 11.

PMID:
18374622
5.

Immunohistochemical and morphometric evaluation of COX 1 and COX-2 in the remodeled lung in idiopathic pulmonary fibrosis and systemic sclerosis.

Parra ER, Lin F, Martins V, Rangel MP, Capelozzi VL.

J Bras Pneumol. 2013 Nov-Dec;39(6):692-700. doi: 10.1590/S1806-37132013000600008. English, Portuguese.

6.

CCL18 in serum, BAL fluid and alveolar macrophage culture supernatant in interstitial lung diseases.

Cai M, Bonella F, He X, Sixt SU, Sarria R, Guzman J, Costabel U.

Respir Med. 2013 Sep;107(9):1444-52. doi: 10.1016/j.rmed.2013.06.004. Epub 2013 Jul 5.

7.

Sphingosine-1-phosphate is increased in patients with idiopathic pulmonary fibrosis and mediates epithelial to mesenchymal transition.

Milara J, Navarro R, Juan G, Peiró T, Serrano A, Ramón M, Morcillo E, Cortijo J.

Thorax. 2012 Feb;67(2):147-56. doi: 10.1136/thoraxjnl-2011-200026. Epub 2011 Nov 21.

PMID:
22106015
8.

Biomarkers to identify ILD and predict lung function decline in scleroderma lung disease or idiopathic pulmonary fibrosis.

Kennedy B, Branagan P, Moloney F, Haroon M, O'Connell OJ, O'Connor TM, O'Regan K, Harney S, Henry MT.

Sarcoidosis Vasc Diffuse Lung Dis. 2015 Sep 14;32(3):228-36.

PMID:
26422568
9.

Lung mast cell density defines a subpopulation of patients with idiopathic pulmonary fibrosis.

Cha SI, Chang CS, Kim EK, Lee JW, Matthay MA, Golden JA, Elicker BM, Jones K, Collard HR, Wolters PJ.

Histopathology. 2012 Jul;61(1):98-106. doi: 10.1111/j.1365-2559.2012.04197.x. Epub 2012 Mar 6.

10.

Elevated levels of platelet derived growth factor and transforming growth factor-beta 1 in bronchoalveolar lavage fluid from patients with scleroderma.

Ludwicka A, Ohba T, Trojanowska M, Yamakage A, Strange C, Smith EA, Leroy EC, Sutherland S, Silver RM.

J Rheumatol. 1995 Oct;22(10):1876-83.

PMID:
8991985
11.

Increased uptake of 111In-octreotide in idiopathic pulmonary fibrosis.

Lebtahi R, Moreau S, Marchand-Adam S, Debray MP, Brauner M, Soler P, Marchal J, Raguin O, Gruaz-Guyon A, Reubi JC, Le Guludec D, Crestani B.

J Nucl Med. 2006 Aug;47(8):1281-7.

12.

[The Role of Bronchoalveolar Lavage in the Diagnosis of Idiopathic Pulmonary Fibrosis: An Investigation of the Relevance of the Protein Content].

Schildge J, Frank J, Klar B.

Pneumologie. 2016 Jul;70(7):435-41. doi: 10.1055/s-0042-107267. Epub 2016 May 24. German.

PMID:
27218212
13.

Regional differences in bronchoalveolar lavage and thoracic high-resolution computed tomography results in dyspneic patients with systemic sclerosis.

Clements PJ, Goldin JG, Kleerup EC, Furst DE, Elashoff RM, Tashkin DP, Roth MD.

Arthritis Rheum. 2004 Jun;50(6):1909-17.

14.

Induced sputum in systemic sclerosis interstitial lung disease: comparison to healthy controls and bronchoalveolar lavage.

Damjanov N, Ostojic P, Kaloudi O, Alari S, Guiducci S, Stanflin N, Nestorovic B, Knezevic J, Camiciottoli G, Porta F, Pistolesi M, Ibba-Manneschi L, Conforti ML, Candelieri A, Matucci Cerinic M.

Respiration. 2009;78(1):56-62. doi: 10.1159/000164720. Epub 2008 Oct 16.

PMID:
18931474
15.

CYFRA 21.1 in bronchoalveolar lavage of idiopathic pulmonary fibrosis patients.

Vercauteren IM, Verleden SE, McDonough JE, Vandermeulen E, Ruttens D, Lammertyn EJ, Bellon H, De Dycker E, Dooms C, Yserbyt J, Verleden GM, Vanaudenaerde BM, Wuyts WA.

Exp Lung Res. 2015;41(8):459-65. doi: 10.3109/01902148.2015.1073407.

PMID:
26381718
16.

Mucin 5B promoter polymorphism is associated with idiopathic pulmonary fibrosis but not with development of lung fibrosis in systemic sclerosis or sarcoidosis.

Stock CJ, Sato H, Fonseca C, Banya WA, Molyneaux PL, Adamali H, Russell AM, Denton CP, Abraham DJ, Hansell DM, Nicholson AG, Maher TM, Wells AU, Lindahl GE, Renzoni EA.

Thorax. 2013 May;68(5):436-41. doi: 10.1136/thoraxjnl-2012-201786. Epub 2013 Jan 15.

PMID:
23321605
17.

Morphological and biochemical properties of alveolar fibroblasts in interstitial lung diseases.

Fireman E, Shahar I, Shoval S, Messer G, Dvash S, Grief J.

Lung. 2001;179(2):105-17.

PMID:
11733853
18.

Oxygen radical production by alveolar inflammatory cells in idiopathic pulmonary fibrosis.

Strausz J, Müller-Quernheim J, Steppling H, Ferlinz R.

Am Rev Respir Dis. 1990 Jan;141(1):124-8.

PMID:
2297170
19.

Circulating monocytes from systemic sclerosis patients with interstitial lung disease show an enhanced profibrotic phenotype.

Mathai SK, Gulati M, Peng X, Russell TR, Shaw AC, Rubinowitz AN, Murray LA, Siner JM, Antin-Ozerkis DE, Montgomery RR, Reilkoff RA, Bucala RJ, Herzog EL.

Lab Invest. 2010 Jun;90(6):812-23. doi: 10.1038/labinvest.2010.73. Epub 2010 Apr 19.

20.

Increased Expression of CC16 in Patients with Idiopathic Pulmonary Fibrosis.

Buendía-Roldán I, Ruiz V, Sierra P, Montes E, Ramírez R, Vega A, Salgado A, Vargas MH, Mejía M, Pardo A, Selman M.

PLoS One. 2016 Dec 15;11(12):e0168552. doi: 10.1371/journal.pone.0168552. eCollection 2016.

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