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Journal Abstract Search

119 related items for PubMed ID: 27496797

  • 1. Comparison of Nasal Potential Difference and Intestinal Current Measurements as Surrogate Markers for CFTR Function.
    Wilschanski M, Yaakov Y, Omari I, Zaman M, Martin CR, Cohen-Cymberknoh M, Shoseyov D, Kerem E, Dasilva D, Sheth S, Uluer A, OʼSullivan BP, Freedman S.
    J Pediatr Gastroenterol Nutr; 2016 Nov; 63(5):e92-e97. PubMed ID: 27496797
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  • 2. Intestinal current measurement versus nasal potential difference measurements for diagnosis of cystic fibrosis: a case-control study.
    Bagheri-Hanson A, Nedwed S, Rueckes-Nilges C, Naehrlich L.
    BMC Pulm Med; 2014 Oct 04; 14():156. PubMed ID: 25280757
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  • 3. Intestinal current measurement for diagnostic classification of patients with questionable cystic fibrosis: validation and reference data.
    Derichs N, Sanz J, Von Kanel T, Stolpe C, Zapf A, Tümmler B, Gallati S, Ballmann M.
    Thorax; 2010 Jul 04; 65(7):594-9. PubMed ID: 20627915
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  • 7. Multicenter intestinal current measurements in rectal biopsies from CF and non-CF subjects to monitor CFTR function.
    Clancy JP, Szczesniak RD, Ashlock MA, Ernst SE, Fan L, Hornick DB, Karp PH, Khan U, Lymp J, Ostmann AJ, Rezayat A, Starner TD, Sugandha SP, Sun H, Quinney N, Donaldson SH, Rowe SM, Gabriel SE.
    PLoS One; 2013 Jul 04; 8(9):e73905. PubMed ID: 24040112
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  • 9. Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport.
    Sermet-Gaudelus I, Girodon E, Sands D, Stremmler N, Vavrova V, Deneuville E, Reix P, Bui S, Huet F, Lebourgeois M, Munck A, Iron A, Skalicka V, Bienvenu T, Roussel D, Lenoir G, Bellon G, Sarles J, Macek M, Roussey M, Fajac I, Edelman A.
    Am J Respir Crit Care Med; 2010 Oct 01; 182(7):929-36. PubMed ID: 20538955
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  • 10. Transepithelial nasal potential difference (NPD) measurements in cystic fibrosis (CF).
    Sands D.
    Med Wieku Rozwoj; 2013 Oct 01; 17(1):13-7. PubMed ID: 23749691
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  • 11. Nasal potential difference: Best or average result for CFTR function as diagnostic criteria for cystic fibrosis?
    Keenan K, Avolio J, Rueckes-Nilges C, Tullis E, Gonska T, Naehrlich L.
    J Cyst Fibros; 2015 May 01; 14(3):310-6. PubMed ID: 25300456
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  • 12. Evaluation of the intestinal current measurement method as a diagnostic test for cystic fibrosis.
    Cohen-Cymberknoh M, Yaakov Y, Shoseyov D, Shteyer E, Schachar E, Rivlin J, Bentur L, Picard E, Aviram M, Israeli E, Kerem E, Wilschanski M.
    Pediatr Pulmonol; 2013 Mar 01; 48(3):229-35. PubMed ID: 22553157
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  • 15. Insights into the variability of nasal potential difference, a biomarker of CFTR activity.
    Kyrilli S, Henry T, Wilschanski M, Fajac I, Davies JC, Jais JP, Sermet-Gaudelus I.
    J Cyst Fibros; 2020 Jul 01; 19(4):620-626. PubMed ID: 31699569
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  • 16. Nasal potential difference outcomes support diagnostic decisions in cystic fibrosis.
    Tridello G, Menin L, Pintani E, Bergamini G, Assael BM, Melotti P.
    J Cyst Fibros; 2016 Sep 01; 15(5):579-82. PubMed ID: 27423539
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  • 17. Ex vivo CF diagnosis by intestinal current measurements (ICM) in small aperture, circulating Ussing chambers.
    De Jonge HR, Ballmann M, Veeze H, Bronsveld I, Stanke F, Tümmler B, Sinaasappel M.
    J Cyst Fibros; 2004 Aug 01; 3 Suppl 2():159-63. PubMed ID: 15463951
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  • 18. Cystic fibrosis in 65- and 67-year-old siblings. Clinical feature and nasal potential difference measurement in patients with genotypes F508del and 2789+5G-->A.
    Mainz J, Hammer U, Rokahr C, Hubler A, Zintl F, Ballmann M.
    Respiration; 2006 Aug 01; 73(5):698-704. PubMed ID: 16763370
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