BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

445 related articles for article (PubMed ID: 23598952)

  • 1. Factors associated with FEV1 decline in cystic fibrosis: analysis of the ECFS patient registry.
    Kerem E; Viviani L; Zolin A; MacNeill S; Hatziagorou E; Ellemunter H; Drevinek P; Gulmans V; Krivec U; Olesen H;
    Eur Respir J; 2014 Jan; 43(1):125-33. PubMed ID: 23598952
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chronic Pseudomonas aeruginosa infection and respiratory muscle impairment in cystic fibrosis.
    Dassios TG; Katelari A; Doudounakis S; Dimitriou G
    Respir Care; 2014 Mar; 59(3):363-70. PubMed ID: 23983273
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Increased rate of lung function decline in Australian adolescents with cystic fibrosis.
    Welsh L; Robertson CF; Ranganathan SC
    Pediatr Pulmonol; 2014 Sep; 49(9):873-7. PubMed ID: 24178906
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Co-colonisation with Aspergillus fumigatus and Pseudomonas aeruginosa is associated with poorer health in cystic fibrosis patients: an Irish registry analysis.
    Reece E; Segurado R; Jackson A; McClean S; Renwick J; Greally P
    BMC Pulm Med; 2017 Apr; 17(1):70. PubMed ID: 28431569
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical expression of cystic fibrosis in a large cohort of Italian siblings.
    Terlizzi V; Lucarelli M; Salvatore D; Angioni A; Bisogno A; Braggion C; Buzzetti R; Carnovale V; Casciaro R; Castaldo G; Cirilli N; Collura M; Colombo C; Di Lullo AM; Elce A; Lucidi V; Madarena E; Padoan R; Quattrucci S; Raia V; Seia M; Termini L; Zarrilli F
    BMC Pulm Med; 2018 Dec; 18(1):196. PubMed ID: 30577776
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chronic Stenotrophomonas maltophilia infection and mortality or lung transplantation in cystic fibrosis patients.
    Waters V; Atenafu EG; Lu A; Yau Y; Tullis E; Ratjen F
    J Cyst Fibros; 2013 Sep; 12(5):482-6. PubMed ID: 23294530
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cystic fibrosis related diabetes in Europe: Prevalence, risk factors and outcome; Olesen et al.
    Olesen HV; Drevinek P; Gulmans VA; Hatziagorou E; Jung A; Mei-Zahav M; Stojnic N; Thomas M; Zolin A;
    J Cyst Fibros; 2020 Mar; 19(2):321-327. PubMed ID: 31680042
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pancreatic enzyme replacement therapy dosing and nutritional outcomes in children with cystic fibrosis.
    Haupt ME; Kwasny MJ; Schechter MS; McColley SA
    J Pediatr; 2014 May; 164(5):1110-1115.e1. PubMed ID: 24560182
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Staphylococcus aureus and Pseudomonas aeruginosa co-infection is associated with cystic fibrosis-related diabetes and poor clinical outcomes.
    Limoli DH; Yang J; Khansaheb MK; Helfman B; Peng L; Stecenko AA; Goldberg JB
    Eur J Clin Microbiol Infect Dis; 2016 Jun; 35(6):947-53. PubMed ID: 26993289
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Risk factors for lung disease progression in children with cystic fibrosis.
    van Horck M; van de Kant K; Winkens B; Wesseling G; Gulmans V; Hendriks H; van der Grinten C; Jöbsis Q; Dompeling E
    Eur Respir J; 2018 Jun; 51(6):. PubMed ID: 29773689
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cystic-fibrosis related-diabetes (CFRD) is preceded by and associated with growth failure and deteriorating lung function.
    Terliesner N; Vogel M; Steighardt A; Gausche R; Henn C; Hentschel J; Kapellen T; Klamt S; Gebhardt J; Kiess W; Prenzel F
    J Pediatr Endocrinol Metab; 2017 Aug; 30(8):815-821. PubMed ID: 28245190
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mucus removal is impaired in children with cystic fibrosis who have been infected by Pseudomonas aeruginosa.
    Laube BL; Sharpless G; Benson J; Carson KA; Mogayzel PJ
    J Pediatr; 2014 Apr; 164(4):839-45. PubMed ID: 24373575
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Effect of allergic bronchopulmonary aspergillosis on FEV
    Kaditis AG; Miligkos M; Bossi A; Colombo C; Hatziagorou E; Kashirskaya N; de Monestrol I; Thomas M; Mei-Zahav M; Chrousos G; Zolin A
    Arch Dis Child; 2017 Aug; 102(8):742-747. PubMed ID: 28325727
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Monitoring clinical and microbiological evolution of a cystic fibrosis patient over 26 years: experience of a Brazilian CF Centre.
    da Costa Ferreira Leite C; Folescu TW; de Cássia Firmida M; Cohen RWF; Leão RS; de Freitas FAD; Albano RM; da Costa CH; Marques EA
    BMC Pulm Med; 2017 Jul; 17(1):100. PubMed ID: 28705217
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Effect of exocrine pancreatic function on resting energy expenditure in cystic fibrosis.
    Moudiou T; Galli-Tsinopoulou A; Nousia-Arvanitakis S
    Acta Paediatr; 2007 Oct; 96(10):1521-5. PubMed ID: 17880419
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Risk factors for cystic fibrosis arthropathy: Data from the German cystic fibrosis registry.
    Grehn C; Dittrich AM; Wosniok J; Holz F; Hafkemeyer S; Naehrlich L; Schwarz C;
    J Cyst Fibros; 2021 Nov; 20(6):e87-e92. PubMed ID: 34034985
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Improvements in lung function outcomes in children with cystic fibrosis are associated with better nutrition, fewer chronic pseudomonas aeruginosa infections, and dornase alfa use.
    McPhail GL; Acton JD; Fenchel MC; Amin RS; Seid M
    J Pediatr; 2008 Dec; 153(6):752-7. PubMed ID: 18760423
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Airway nitric oxide in patients with cystic fibrosis is associated with pancreatic function, Pseudomonas infection, and polyunsaturated fatty acids.
    Keen C; Olin AC; Edentoft A; Gronowitz E; Strandvik B
    Chest; 2007 Jun; 131(6):1857-64. PubMed ID: 17400678
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Bronchiectases at early chest computed tomography in children with cystic fibrosis are associated with increased risk of subsequent pulmonary exacerbations and chronic pseudomonas infection.
    Bortoluzzi CF; Volpi S; D'Orazio C; Tiddens HA; Loeve M; Tridello G; Assael BM
    J Cyst Fibros; 2014 Sep; 13(5):564-71. PubMed ID: 24726420
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association between genotype and pulmonary phenotype in cystic fibrosis patients with severe mutations.
    Geborek A; Hjelte L
    J Cyst Fibros; 2011 May; 10(3):187-92. PubMed ID: 21354377
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.