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Journal Abstract Search

261 related items for PubMed ID: 17469152

  • 1. Amiloride-insensitive nasal potential difference varies with the menstrual cycle in cystic fibrosis.
    Sweezey NB, Smith D, Corey M, Ellis L, Carpenter S, Tullis DE, Durie P, O'Brodovich HM.
    Pediatr Pulmonol; 2007 Jun; 42(6):519-24. PubMed ID: 17469152
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  • 3. Measurement of airway ion transport assists the diagnosis of cystic fibrosis.
    Middleton PG, House HH.
    Pediatr Pulmonol; 2010 Aug; 45(8):789-95. PubMed ID: 20597077
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  • 4. Parallel improvement of sodium and chloride transport defects by miglustat (n-butyldeoxynojyrimicin) in cystic fibrosis epithelial cells.
    Noël S, Wilke M, Bot AG, De Jonge HR, Becq F.
    J Pharmacol Exp Ther; 2008 Jun; 325(3):1016-23. PubMed ID: 18309088
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  • 5. Basic protocol for transepithelial nasal potential difference measurements.
    Schüler D, Sermet-Gaudelus I, Wilschanski M, Ballmann M, Dechaux M, Edelman A, Hug M, Leal T, Lebacq J, Lebecque P, Lenoir G, Stanke F, Wallemacq P, Tümmler B, Knowles MR.
    J Cyst Fibros; 2004 Aug; 3 Suppl 2():151-5. PubMed ID: 15463949
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  • 8. Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis.
    Knowles M, Gatzy J, Boucher R.
    N Engl J Med; 1981 Dec 17; 305(25):1489-95. PubMed ID: 7300874
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  • 11. Acidic pH hyperpolarizes nasal potential difference.
    Uwaifo O, Bamford P, Zeitlin PL, Blaisdell CJ.
    Pediatr Pulmonol; 2006 Feb 17; 41(2):151-7. PubMed ID: 16369925
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  • 12. Exercise reduces airway sodium ion reabsorption in cystic fibrosis but not in exercise asthma.
    Schmitt L, Wiebel M, Frese F, Dehnert C, Zugck C, Bärtsch P, Mairbäurl H.
    Eur Respir J; 2011 Feb 17; 37(2):342-8. PubMed ID: 20525718
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  • 13. Effect of macrolides on in vivo ion transport across cystic fibrosis nasal epithelium.
    Barker PM, Gillie DJ, Schechter MS, Rubin BK.
    Am J Respir Crit Care Med; 2005 Apr 15; 171(8):868-71. PubMed ID: 15657462
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  • 14. Minor role of Cl- secretion in non-cystic fibrosis and cystic fibrosis human nasal epithelium.
    Rückes-Nilges C, Weber U, Lindemann H, Münker G, Clauss W, Weber WM.
    Cell Physiol Biochem; 1999 Apr 15; 9(1):1-10. PubMed ID: 10352340
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  • 15. N-acetylcysteine inhibits Na+ absorption across human nasal epithelial cells.
    Rochat T, Lacroix JS, Jornot L.
    J Cell Physiol; 2004 Oct 15; 201(1):106-16. PubMed ID: 15281093
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  • 17. Nasal airway ion transport is linked to the cystic fibrosis phenotype in adult patients.
    Fajac I, Hubert D, Guillemot D, Honoré I, Bienvenu T, Volter F, Dall'Ava-Santucci J, Dusser DJ.
    Thorax; 2004 Nov 15; 59(11):971-6. PubMed ID: 15516474
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  • 18. Protocols for in vivo measurement of the ion transport defects in cystic fibrosis nasal epithelium.
    Middleton PG, Geddes DM, Alton EW.
    Eur Respir J; 1994 Nov 15; 7(11):2050-6. PubMed ID: 7875281
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  • 19. Effects of topically delivered benzamil and amiloride on nasal potential difference in cystic fibrosis.
    Hofmann T, Stutts MJ, Ziersch A, Rückes C, Weber WM, Knowles MR, Lindemann H, Boucher RC.
    Am J Respir Crit Care Med; 1998 Jun 15; 157(6 Pt 1):1844-9. PubMed ID: 9620916
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  • 20. Relationship between airway ion transport and a mild pulmonary disease mutation in CFTR.
    Walker LC, Venglarik CJ, Aubin G, Weatherly MR, McCarty NA, Lesnick B, Ruiz F, Clancy JP, Sorscher EJ.
    Am J Respir Crit Care Med; 1997 May 15; 155(5):1684-9. PubMed ID: 9154877
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