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Journal Abstract Search

538 related items for PubMed ID: 29370786

  • 1. 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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  • 2. Baseline characteristics of idiopathic pulmonary fibrosis: analysis from the Australian Idiopathic Pulmonary Fibrosis Registry.
    Jo HE, Glaspole I, Grainge C, Goh N, Hopkins PM, Moodley Y, Reynolds PN, Chapman S, Walters EH, Zappala C, Allan H, Keir GJ, Hayen A, Cooper WA, Mahar AM, Ellis S, Macansh S, Corte TJ.
    Eur Respir J; 2017 Feb 25; 49(2):. PubMed ID: 28232409
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  • 3. Baseline characteristics and survival of patients of idiopathic pulmonary fibrosis: a longitudinal analysis of the Swedish IPF Registry.
    Gao J, Kalafatis D, Carlson L, Pesonen IHA, Li CX, Wheelock Å, Magnusson JM, Sköld CM.
    Respir Res; 2021 Feb 05; 22(1):40. PubMed ID: 33546682
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  • 4. EMPIRE Registry, Czech Part: Impact of demographics, pulmonary function and HRCT on survival and clinical course in idiopathic pulmonary fibrosis.
    Doubková M, Švancara J, Svoboda M, Šterclová M, Bartoš V, Plačková M, Lacina L, Žurková M, Binková I, Bittenglová R, Lošťáková V, Merta Z, Šišková L, Tyl R, Lisá P, Šuldová H, Petřík F, Pšikalová J, Řihák V, Snížek T, Reiterer P, Homolka J, Musilová P, Lněnička J, Palúch P, Hrdina R, Králová R, Hortvíková H, Strenková J, Vašáková M.
    Clin Respir J; 2018 Apr 05; 12(4):1526-1535. PubMed ID: 28862397
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  • 9. 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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  • 10. 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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  • 14. [Idiopathic pulmonary fibrosis prognostic factors - analysis of the Czech registry].
    Doubková M, Uher M, Bartoš V, Šterclová M, Lacina L, Lošťáková V, Binková I, Plačková M, Žurková M, Bittenglová R, Pšikalová J, Šišková L, Lisá P, Petřík F, Polák J, Řihák V, Skřičková J, Vašáková M.
    Cas Lek Cesk; 2016 Apr 29; 155(4):22-8. PubMed ID: 27481198
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  • 15. Idiopathic pulmonary fibrosis patients with severe physiologic impairment: characteristics and outcomes.
    Pastre J, Barnett S, Ksovreli I, Taylor J, Brown AW, Shlobin OA, Ahmad K, Khangoora V, Aryal S, King CS, Nathan SD.
    Respir Res; 2021 Jan 06; 22(1):5. PubMed ID: 33407450
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  • 19. Longitudinal clinical outcomes in a real-world population of patients with idiopathic pulmonary fibrosis: the PROOF registry.
    Wuyts WA, Dahlqvist C, Slabbynck H, Schlesser M, Gusbin N, Compere C, Maddens S, Lee YC, Kirchgaessler KU, Bartley K, Bondue B.
    Respir Res; 2019 Oct 24; 20(1):231. PubMed ID: 31651324
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