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Journal Abstract Search

211 related items for PubMed ID: 31331863

  • 1. 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; 19(4):627-631. PubMed ID: 31331863
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  • 2. Measurement of nasal potential difference in young children with an equivocal sweat test following newborn screening for cystic fibrosis.
    Sermet-Gaudelus I, Girodon E, Roussel D, Deneuville E, Bui S, Huet F, Guillot M, Aboutaam R, Renouil M, Munck A, des Georges M, Iron A, Thauvin-Robinet C, Fajac I, Lenoir G, Roussey M, Edelman A.
    Thorax; 2010 Jun; 65(6):539-44. PubMed ID: 20522854
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  • 4. 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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  • 10. 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 04; 42(7):810-4. PubMed ID: 18360295
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  • 13. 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 04; 13(2):129-135. PubMed ID: 28194692
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  • 14. Uncertainty in the diagnosis of cystic fibrosis: possible role of in vivo nasal potential difference measurements.
    Wilson DC, Ellis L, Zielenski J, Corey M, Ip WF, Tsui LC, Tullis E, Knowles MR, Durie PR.
    J Pediatr; 1998 Apr 04; 132(4):596-9. PubMed ID: 9580755
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  • 15. Lung disease associated with the IVS8 5T allele of the CFTR gene.
    Noone PG, Pue CA, Zhou Z, Friedman KJ, Wakeling EL, Ganeshananthan M, Simon RH, Silverman LM, Knowles MR.
    Am J Respir Crit Care Med; 2000 Nov 04; 162(5):1919-24. PubMed ID: 11069835
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  • 16. A pilot clinical trial of oral sodium 4-phenylbutyrate (Buphenyl) in deltaF508-homozygous cystic fibrosis patients: partial restoration of nasal epithelial CFTR function.
    Rubenstein RC, Zeitlin PL.
    Am J Respir Crit Care Med; 1998 Feb 04; 157(2):484-90. PubMed ID: 9476862
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  • 18. N1303K and IVS8-5T, clinical presentation within a family with atypical cystic fibrosis.
    Van Hoorenbeeck K, Storm K, van den Ende J, Biervliet M, Desager KN.
    J Cyst Fibros; 2007 May 04; 6(3):220-2. PubMed ID: 17127107
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