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Journal Abstract Search

211 related items for PubMed ID: 25280757

  • 1. 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. 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 04; 63(5):e92-e97. PubMed ID: 27496797
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  • 4. Does integration of various ion channel measurements improve diagnostic performance in cystic fibrosis?
    Ooi CY, Dupuis A, Gonska T, Ellis L, Ni A, Jarvi K, Martin S, Ray P, Steele L, Kortan P, Dorfman R, Solomon M, Zielenski J, Corey M, Tullis E, Durie P.
    Ann Am Thorac Soc; 2014 May 04; 11(4):562-70. PubMed ID: 24697796
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  • 5. The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening.
    Sermet-Gaudelus I, Roussel D, Bui S, Deneuville E, Huet F, Reix P, Bellon G, Lenoir G, Edelman A.
    BMC Pediatr; 2006 Oct 03; 6():25. PubMed ID: 17018149
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  • 6. Intestinal current measurement and nasal potential difference to make a diagnosis of cases with inconclusive CFTR genetics and sweat test.
    Minso R, Schulz A, Dopfer C, Alfeis N, Barneveld AV, Makartian-Gyulumyan L, Hansen G, Junge S, Müller C, Ringshausen FCC, Sauer-Heilborn A, Stanke F, Stolpe C, Tamm S, Welte T, Dittrich AM, Tümmler B.
    BMJ Open Respir Res; 2020 Oct 03; 7(1):. PubMed ID: 33020115
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  • 7. Nasal potential difference in suspected cystic fibrosis patients with 5T polymorphism.
    Aalbers BL, Yaakov Y, Derichs N, Simmonds NJ, De Wachter E, Melotti P, De Boeck K, Leal T, Tümmler B, Wilschanski M, Bronsveld I.
    J Cyst Fibros; 2020 Jul 03; 19(4):627-631. PubMed ID: 31331863
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  • 11. Relevance of nasal potential difference in diagnosis of cystic fibrosis among children.
    Valiulis A, Skurvydienė I, Misevičienė V, Kasnauskienė J, Vaidelienė L, Utkus A.
    Medicina (Kaunas); 2013 Jul 03; 49(4):185-90. PubMed ID: 23985983
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  • 12. Cystic fibrosis transmembrane conductance regulator ion channel function testing in recurrent acute pancreatitis.
    Segal I, Yaakov Y, Adler SN, Blau H, Broide E, Santo M, Yahav Y, Klar A, Lerner A, Aviram M, Ellis I, Mountford R, Shteyer E, Kerem E, Wilschanski M.
    J Clin Gastroenterol; 2008 Aug 03; 42(7):810-4. PubMed ID: 18360295
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  • 14. Sweat gland bioelectrics differ in cystic fibrosis: a new concept for potential diagnosis and assessment of CFTR function in cystic fibrosis.
    Gonska T, Ip W, Turner D, Han WS, Rose J, Durie P, Quinton P.
    Thorax; 2009 Nov 03; 64(11):932-8. PubMed ID: 19734129
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  • 15. Role of CFTR mutation analysis in the diagnostic algorithm for cystic fibrosis.
    Ratkiewicz M, Pastore M, McCoy KS, Thompson R, Hayes D, Sheikh SI.
    World J Pediatr; 2017 Apr 03; 13(2):129-135. PubMed ID: 28194692
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  • 17. 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 Apr 03; 73(5):698-704. PubMed ID: 16763370
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  • 18. In vivo and in vitro ivacaftor response in cystic fibrosis patients with residual CFTR function: N-of-1 studies.
    McGarry ME, Illek B, Ly NP, Zlock L, Olshansky S, Moreno C, Finkbeiner WE, Nielson DW.
    Pediatr Pulmonol; 2017 Apr 03; 52(4):472-479. PubMed ID: 28068001
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