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Journal Abstract Search

426 related items for PubMed ID: 28100601

  • 1. Use of Selective Fungal Culture Media Increases Rates of Detection of Fungi in the Respiratory Tract of Cystic Fibrosis Patients.
    Hong G, Miller HB, Allgood S, Lee R, Lechtzin N, Zhang SX.
    J Clin Microbiol; 2017 Apr; 55(4):1122-1130. PubMed ID: 28100601
    [Abstract] [Full Text] [Related]

  • 2. Detection of hyphomycetes in the upper respiratory tract of patients with cystic fibrosis.
    Horré R, Marklein G, Siekmeier R, Reiffert SM.
    Mycoses; 2011 Nov; 54(6):514-22. PubMed ID: 20492536
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  • 3. Toward the Standardization of Mycological Examination of Sputum Samples in Cystic Fibrosis: Results from a French Multicenter Prospective Study.
    Coron N, Pihet M, Fréalle E, Lemeille Y, Pinel C, Pelloux H, Gargala G, Favennec L, Accoceberry I, Durand-Joly I, Dalle F, Huet F, Fanton A, Boldron A, Loeuille GA, Domblides P, Coltey B, Pin I, Llerena C, Troussier F, Person C, Marguet C, Wizla N, Thumerelle C, Turck D, Bui S, Fayon M, Duhamel A, Prévotat A, Wallaert B, Leroy S, Bouchara JP, Delhaes L.
    Mycopathologia; 2018 Feb; 183(1):101-117. PubMed ID: 28748285
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  • 4. Modified culture method detects a high diversity of fungal species in cystic fibrosis patients.
    Masoud-Landgraf L, Badura A, Eber E, Feierl G, Marth E, Buzina W.
    Med Mycol; 2014 Feb; 52(2):179-86. PubMed ID: 23651180
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  • 5. Prevalence and diversity of filamentous fungi in the airways of cystic fibrosis patients - A Dutch, multicentre study.
    Engel TGP, Slabbers L, de Jong C, Melchers WJG, Hagen F, Verweij PE, Merkus P, Meis JF, Dutch Cystic Fibrosis Fungal Collection Consortium.
    J Cyst Fibros; 2019 Mar; 18(2):221-226. PubMed ID: 30514613
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  • 6. Development of selective media for the isolation of yeasts and filamentous fungi from the sputum of adult patients with cystic fibrosis (CF).
    Nagano Y, Millar BC, Goldsmith CE, Walker JM, Elborn JS, Rendall J, Moore JE.
    J Cyst Fibros; 2008 Nov; 7(6):566-72. PubMed ID: 18723404
    [Abstract] [Full Text] [Related]

  • 7. Exophiala (Wangiella) dermatitidis and cystic fibrosis - Prevalence and risk factors.
    Lebecque P, Leonard A, Huang D, Reychler G, Boeras A, Leal T, Symoens F.
    Med Mycol; 2010 Nov; 48 Suppl 1():S4-9. PubMed ID: 21067329
    [Abstract] [Full Text] [Related]

  • 8. Selective isolation of Pseudallescheria and Scedosporium species from respiratory tract specimens of cystic fibrosis patients.
    Horré R, Marklein G, Siekmeier R, Nidermajer S, Reiffert SM.
    Respiration; 2009 Nov; 77(3):320-4. PubMed ID: 18957840
    [Abstract] [Full Text] [Related]

  • 9. Comparison of techniques to examine the diversity of fungi in adult patients with cystic fibrosis.
    Nagano Y, Elborn JS, Millar BC, Walker JM, Goldsmith CE, Rendall J, Moore JE.
    Med Mycol; 2010 Feb; 48(1):166-76.e1. PubMed ID: 19672783
    [Abstract] [Full Text] [Related]

  • 10. Characteristics of pathogenic fungi and antifungal therapy in cystic fibrosis.
    Müller FM, Seidler M.
    Expert Rev Anti Infect Ther; 2010 Aug; 8(8):957-64. PubMed ID: 20695750
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  • 12. Lack of standardization in the procedures for mycological examination of sputum samples from CF patients: a possible cause for variations in the prevalence of filamentous fungi.
    Borman AM, Palmer MD, Delhaes L, Carrère J, Favennec L, Ranque S, Gangneux JP, Horré R, Bouchara JP.
    Med Mycol; 2010 Nov; 48 Suppl 1():S88-97. PubMed ID: 21067335
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  • 14. Direct detection of Exophiala and Scedosporium species in sputa of patients with cystic fibrosis.
    Chen M, Kondori N, Deng S, Gerrits van den Ende AHG, Lackner M, Liao W, de Hoog GS.
    Med Mycol; 2018 Aug 01; 56(6):695-702. PubMed ID: 29228273
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  • 15. Airway colonisation by Candida and Aspergillus species in Iranian cystic fibrosis patients.
    Nasri E, Fakhim H, Vaezi A, Khalilzadeh S, Ahangarkani F, Laal Kargar M, Abtahian Z, Badali H.
    Mycoses; 2019 May 01; 62(5):434-440. PubMed ID: 30681747
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  • 20. Development of a novel PCR assay for the identification of the black yeast, Exophiala (Wangiella) dermatitidis from adult patients with cystic fibrosis (CF).
    Nagano Y, Elborn JS, Millar BC, Goldsmith CE, Rendall J, Moore JE.
    J Cyst Fibros; 2008 Nov 01; 7(6):576-80. PubMed ID: 18571996
    [Abstract] [Full Text] [Related]

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