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Journal Abstract Search
200 related items for PubMed ID: 28152602
1. Feasibility of Early Detection of Cystic Fibrosis Acute Pulmonary Exacerbations by Exhaled Breath Condensate Metabolomics: A Pilot Study. Zang X, Monge ME, McCarty NA, Stecenko AA, Fernández FM. J Proteome Res; 2017 Feb 03; 16(2):550-558. PubMed ID: 28152602 [Abstract] [Full Text] [Related]
2. Early Detection of Cystic Fibrosis Acute Pulmonary Exacerbations by Exhaled Breath Condensate Metabolomics. Zang X, Monge ME, Gaul DA, McCarty NA, Stecenko A, Fernández FM. J Proteome Res; 2020 Jan 03; 19(1):144-152. PubMed ID: 31621328 [Abstract] [Full Text] [Related]
3. Comparison of Ambient and Atmospheric Pressure Ion Sources for Cystic Fibrosis Exhaled Breath Condensate Ion Mobility-Mass Spectrometry Metabolomics. Zang X, Pérez JJ, Jones CM, Monge ME, McCarty NA, Stecenko AA, Fernández FM. J Am Soc Mass Spectrom; 2017 Aug 03; 28(8):1489-1496. PubMed ID: 28364225 [Abstract] [Full Text] [Related]
4. Asymmetric dimethylarginine and related metabolites in exhaled breath condensate of children with cystic fibrosis. Lucca F, Da Dalt L, Ros M, Gucciardi A, Pirillo P, Naturale M, Perilongo G, Giordano G, Baraldi E. Clin Respir J; 2018 Jan 03; 12(1):140-148. PubMed ID: 27216780 [Abstract] [Full Text] [Related]
10. Biomarkers in exhaled breath condensate indicate presence and severity of cystic fibrosis in children. Robroeks CM, Rosias PP, van Vliet D, Jöbsis Q, Yntema JB, Brackel HJ, Damoiseaux JG, den Hartog GM, Wodzig WK, Dompeling E. Pediatr Allergy Immunol; 2008 Nov 03; 19(7):652-9. PubMed ID: 18312532 [Abstract] [Full Text] [Related]
11. Plasma metabolomics in adults with cystic fibrosis during a pulmonary exacerbation: A pilot randomized study of high-dose vitamin D3 administration. Alvarez JA, Chong EY, Walker DI, Chandler JD, Michalski ES, Grossmann RE, Uppal K, Li S, Frediani JK, Tirouvanziam R, Tran VT, Tangpricha V, Jones DP, Ziegler TR. Metabolism; 2017 May 03; 70():31-41. PubMed ID: 28403943 [Abstract] [Full Text] [Related]
12. Distinctive metabolic profiles between Cystic Fibrosis mutational subclasses and lung function. Masood A, Jacob M, Gu X, Abdel Jabar M, Benabdelkamel H, Nizami I, Li L, Dasouki M, Abdel Rahman AM. Metabolomics; 2021 Jan 04; 17(1):4. PubMed ID: 33394183 [Abstract] [Full Text] [Related]
13. Exhaled breath condensate pH and ammonia in cystic fibrosis and response to treatment of acute pulmonary exacerbations. Newport S, Amin N, Dozor AJ. Pediatr Pulmonol; 2009 Sep 04; 44(9):866-72. PubMed ID: 19670404 [Abstract] [Full Text] [Related]