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Journal Abstract Search


335 related items for PubMed ID: 25862941

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  • 4. Change in forced vital capacity and associated subsequent outcomes in patients with newly diagnosed idiopathic pulmonary fibrosis.
    Reichmann WM, Yu YF, Macaulay D, Wu EQ, Nathan SD.
    BMC Pulm Med; 2015 Dec 29; 15():167. PubMed ID: 26714746
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  • 6. Marginal decline in forced vital capacity is associated with a poor outcome in idiopathic pulmonary fibrosis.
    Zappala CJ, Latsi PI, Nicholson AG, Colby TV, Cramer D, Renzoni EA, Hansell DM, du Bois RM, Wells AU.
    Eur Respir J; 2010 Apr 29; 35(4):830-6. PubMed ID: 19840957
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  • 9. Risk factors for acute exacerbation of idiopathic pulmonary fibrosis: A systematic review and meta-analysis.
    Qiu M, Chen Y, Ye Q.
    Clin Respir J; 2018 Mar 29; 12(3):1084-1092. PubMed ID: 28332341
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  • 10. Composite Physiologic Index, Percent Forced Vital Capacity and Percent Diffusing Capacity for Carbon Monoxide Could Be Predictors of Pirfenidone Tolerability in Patients with Idiopathic Pulmonary Fibrosis.
    Konishi S, Arita M, Ito I, Tachibana H, Takaiwa T, Fukuda Y, Watanabe N, Tsubouchi K, Masuda G, Tanaka M, Kourogi Y, Kunimasa K, Nishiyama A, Iwasaku M, Ito A, Tokioka F, Yoshioka H, Hashimoto T, Ishida T.
    Intern Med; 2015 Mar 29; 54(22):2835-41. PubMed ID: 26567995
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  • 12. Disease progression in idiopathic pulmonary fibrosis without pulmonary function impairment.
    Kondoh Y, Taniguchi H, Ogura T, Johkoh T, Fujimoto K, Sumikawa H, Kataoka K, Baba T, Colby TV, Kitaichi M.
    Respirology; 2013 Jul 29; 18(5):820-6. PubMed ID: 23489318
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  • 13. Disease progression in idiopathic pulmonary fibrosis with mild physiological impairment: analysis from the Australian IPF registry.
    Jo HE, Glaspole I, Moodley Y, Chapman S, Ellis S, Goh N, Hopkins P, Keir G, Mahar A, Cooper W, Reynolds P, Haydn Walters E, Zappala C, Grainge C, Allan H, Macansh S, Corte TJ.
    BMC Pulm Med; 2018 Jan 25; 18(1):19. PubMed ID: 29370786
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  • 14. Baseline KL-6 predicts increased risk for acute exacerbation of idiopathic pulmonary fibrosis.
    Ohshimo S, Ishikawa N, Horimasu Y, Hattori N, Hirohashi N, Tanigawa K, Kohno N, Bonella F, Guzman J, Costabel U.
    Respir Med; 2014 Jul 25; 108(7):1031-9. PubMed ID: 24835074
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  • 15. Serum carcinoembryonic antigen correlates with severity of idiopathic pulmonary fibrosis.
    Fahim A, Crooks MG, Wilmot R, Campbell AP, Morice AH, Hart SP.
    Respirology; 2012 Nov 25; 17(8):1247-52. PubMed ID: 22816375
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  • 16. Predictors of acute exacerbation in biopsy-proven idiopathic pulmonary fibrosis.
    Kishaba T, Hozumi H, Fujisawa T, Nei Y, Enomoto N, Sugiura H, Kitani M, Suda T.
    Respir Investig; 2020 May 25; 58(3):177-184. PubMed ID: 32205147
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  • 17. The serum KL-6 levels in untreated idiopathic pulmonary fibrosis can naturally decline in association with disease progression.
    Ishii H, Kushima H, Kinoshita Y, Fujita M, Watanabe K.
    Clin Respir J; 2018 Sep 25; 12(9):2411-2418. PubMed ID: 30015394
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