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Journal Abstract Search

232 related items for PubMed ID: 32022432

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  • 2. Non-invasive assessment of upper and lower airway infection and inflammation in CF patients.
    Fischer N, Hentschel J, Markert UR, Keller PM, Pletz MW, Mainz JG.
    Pediatr Pulmonol; 2014 Nov; 49(11):1065-75. PubMed ID: 24464968
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  • 4. Concordant genotype of upper and lower airways P aeruginosa and S aureus isolates in cystic fibrosis.
    Mainz JG, Naehrlich L, Schien M, Käding M, Schiller I, Mayr S, Schneider G, Wiedemann B, Wiehlmann L, Cramer N, Pfister W, Kahl BC, Beck JF, Tümmler B.
    Thorax; 2009 Jun; 64(6):535-40. PubMed ID: 19282318
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  • 6. Upper and lower airway cultures in children with cystic fibrosis: do not neglect the upper airways.
    Bonestroo HJ, de Winter-de Groot KM, van der Ent CK, Arets HG.
    J Cyst Fibros; 2010 Mar; 9(2):130-4. PubMed ID: 20110197
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  • 10. NET formation induced by Pseudomonas aeruginosa cystic fibrosis isolates measured as release of myeloperoxidase-DNA and neutrophil elastase-DNA complexes.
    Yoo DG, Floyd M, Winn M, Moskowitz SM, Rada B.
    Immunol Lett; 2014 Aug; 160(2):186-94. PubMed ID: 24670966
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  • 11. BPI-ANCA is expressed in the airways of cystic fibrosis patients and correlates to platelet numbers and Pseudomonas aeruginosa colonization.
    Hovold G, Lindberg U, Ljungberg JK, Shannon O, Påhlman LI.
    Respir Med; 2020 Aug; 170():105994. PubMed ID: 32843162
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  • 13. Inflammatory and immunological biomarkers are not related to survival in adults with Cystic Fibrosis.
    Moffitt KL, Martin SL, Jones AM, Webb AK, Cardwell C, Tunney MM, Elborn JS.
    J Cyst Fibros; 2014 Jan; 13(1):63-8. PubMed ID: 23860440
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  • 15. Antibody responses to lipid A, core, and O sugars of the Pseudomonas aeruginosa lipopolysaccharide in chronically infected cystic fibrosis patients.
    Kronborg G, Fomsgaard A, Galanos C, Freudenberg MA, Høiby N.
    J Clin Microbiol; 1992 Jul; 30(7):1848-55. PubMed ID: 1378455
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  • 16. Host inflammatory responses to first isolation of Pseudomonas aeruginosa from sputum in cystic fibrosis.
    Elborn JS, Cordon SM, Shale DJ.
    Pediatr Pulmonol; 1993 May; 15(5):287-91. PubMed ID: 8327287
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  • 17. IgA and IgG antibodies against surface antigens of Pseudomonas aeruginosa in sputum and serum from patients with cystic fibrosis.
    Schiøtz PO, Høiby N, Permin H, Wiik A.
    Acta Pathol Microbiol Scand C; 1979 Jun; 87C(3):229-33. PubMed ID: 113981
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  • 19. Assessment of pulmonary antibodies with induced sputum and bronchoalveolar lavage induced by nasal vaccination against Pseudomonas aeruginosa: a clinical phase I/II study.
    Baumann U, Göcke K, Gewecke B, Freihorst J, von Specht BU.
    Respir Res; 2007 Aug 05; 8(1):57. PubMed ID: 17683588
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  • 20. Serum IgG and sputum IgA antibody to core lipopolysaccharide antigen from Pseudomonas cepacia in patients with cystic fibrosis.
    Nelson JW, Butler SL, Brown PH, Greening AP, Govan JR.
    J Med Microbiol; 1993 Jul 05; 39(1):39-47. PubMed ID: 7686977
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