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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1961 1
1965 1
2005 1
2008 1
2009 1
2010 2
2011 4
2012 2
2015 2
2017 3
2018 1
2019 2
2020 1
2021 3
2022 5
2023 1

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Page 1
British Lung Foundation/United Kingdom Primary Immunodeficiency Network Consensus Statement on the Definition, Diagnosis, and Management of Granulomatous-Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency Disorders.
Hurst JR, Verma N, Lowe D, Baxendale HE, Jolles S, Kelleher P, Longhurst HJ, Patel SY, Renzoni EA, Sander CR, Avery GR, Babar JL, Buckland MS, Burns S, Egner W, Gompels MM, Gordins P, Haddock JA, Hart SP, Hayman GR, Herriot R, Hoyles RK, Huissoon AP, Jacob J, Nicholson AG, Rassl DM, Sargur RB, Savic S, Seneviratne SL, Sheaff M, Vaitla PM, Walters GI, Whitehouse JL, Wright PA, Condliffe AM. Hurst JR, et al. Among authors: whitehouse jl. J Allergy Clin Immunol Pract. 2017 Jul-Aug;5(4):938-945. doi: 10.1016/j.jaip.2017.01.021. Epub 2017 Mar 25. J Allergy Clin Immunol Pract. 2017. PMID: 28351785 Free article. Review.
Retinopathy and microalbuminuria are common microvascular complications in cystic fibrosis-related diabetes.
Kempegowda P, Sunsoa H, Chandan JS, Quinn LM, Amrelia PM, Atta SN, Amir S, Teh YS, Chaudhry S, de Bray A, Rashid R, Whitehouse JL, Nash EF, Syed A. Kempegowda P, et al. Among authors: whitehouse jl. Ther Adv Endocrinol Metab. 2020 Oct 21;11:2042018820966428. doi: 10.1177/2042018820966428. eCollection 2020. Ther Adv Endocrinol Metab. 2020. PMID: 35154634 Free PMC article.
Novel detection of specific bacterial quorum sensing molecules in saliva: Potential non-invasive biomarkers for pulmonary Pseudomonas aeruginosa in cystic fibrosis.
Webb K, Cámara M, Zain NMM, Halliday N, Bruce KD, Nash EF, Whitehouse JL, Knox A, Forrester D, Smyth AR, Williams P, Fogarty A, Barr HL. Webb K, et al. Among authors: whitehouse jl. J Cyst Fibros. 2022 Jul;21(4):626-629. doi: 10.1016/j.jcf.2021.08.030. Epub 2021 Sep 11. J Cyst Fibros. 2022. PMID: 34518117
Porphyromonas pasteri and Prevotella nanceiensis in the sputum microbiota are associated with increased decline in lung function in individuals with cystic fibrosis.
Webb K, Zain NMM, Stewart I, Fogarty A, Nash EF, Whitehouse JL, Smyth AR, Lilley AK, Knox A, Williams P, Cámara M, Bruce K, Barr HL. Webb K, et al. Among authors: whitehouse jl. J Med Microbiol. 2022 Feb;71(2):001481. doi: 10.1099/jmm.0.001481. J Med Microbiol. 2022. PMID: 35113780 Free PMC article.
2-Alkyl-4-quinolone quorum sensing molecules are biomarkers for culture-independent Pseudomonas aeruginosa burden in adults with cystic fibrosis.
Zain NMM, Webb K, Stewart I, Halliday N, Barrett DA, Nash EF, Whitehouse JL, Honeybourne D, Smyth AR, Forrester DL, Knox AJ, Williams P, Fogarty A, Cámara M, Bruce KD, Barr HL. Zain NMM, et al. Among authors: whitehouse jl. J Med Microbiol. 2021 Oct;70(10):001420. doi: 10.1099/jmm.0.001420. J Med Microbiol. 2021. PMID: 34596013 Free PMC article.
27 results