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Journal Abstract Search

189 related items for PubMed ID: 23985983

  • 21.
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  • 22. CFTR genotype and clinical outcomes of adult patients carried as cystic fibrosis disease.
    Bonadia LC, de Lima Marson FA, Ribeiro JD, Paschoal IA, Pereira MC, Ribeiro AF, Bertuzzo CS.
    Gene; 2014 May 01; 540(2):183-90. PubMed ID: 24583165
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  • 23. Nasal potential difference in congenital bilateral absence of the vas deferens.
    Pradal U, Castellani C, Delmarco A, Mastella G.
    Am J Respir Crit Care Med; 1998 Sep 01; 158(3):896-901. PubMed ID: 9731023
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  • 24. Modified method to measure nasal potential difference.
    Leal T, Lebacq J, Lebecque P, Cumps J, Wallemacq P.
    Clin Chem Lab Med; 2003 Jan 01; 41(1):61-7. PubMed ID: 12636051
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  • 26. 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 01; 132(4):596-9. PubMed ID: 9580755
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  • 27. Nasal potential difference in cystic fibrosis considering severe CFTR mutations.
    Ng RT, Marson FA, Ribeiro JD, Ribeiro AF, Bertuzzo CS, Ribeiro MA, Severino SD, Sakano E.
    Dis Markers; 2015 Apr 01; 2015():306825. PubMed ID: 25667564
    [Abstract] [Full Text] [Related]

  • 28. β-adrenergic sweat test in children with inconclusive cystic fibrosis diagnosis: Do we need new reference ranges?
    Zampoli M, Verstraete J, Nguyen-Khoa T, Sermet-Gaudelus I, Zar HJ, Gonska T, Morrow BM.
    Pediatr Pulmonol; 2023 Jan 01; 58(1):187-196. PubMed ID: 36193559
    [Abstract] [Full Text] [Related]

  • 29. [Nasal potential difference test to diagnose cystic fibrosis].
    Domingo-Ribas C, Bosque-García M.
    Arch Bronconeumol; 2006 Jan 01; 42(1):33-8. PubMed ID: 16426521
    [Abstract] [Full Text] [Related]

  • 30. 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 01; 42(7):810-4. PubMed ID: 18360295
    [Abstract] [Full Text] [Related]

  • 31. Serum lipase levels as a diagnostic marker in cystic fibrosis patients with normal or borderline sweat tests.
    Augarten A, Shmilovich H, Doolman R, Aviram M, Akons H, Ben Tur L, Blau H, Kerem E, Rivlin J, Sela BA, Szeinberg A, Yahav Y.
    Pediatr Pulmonol; 2000 Oct 01; 30(4):320-3. PubMed ID: 11015133
    [Abstract] [Full Text] [Related]

  • 32. Diagnosing cystic fibrosis in newborn screening in Poland - 15 years of experience.
    Sands D, Zybert K, Mierzejewska E, Ołtarzewski M.
    Dev Period Med; 2015 Oct 01; 19(1):16-24. PubMed ID: 26003066
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  • 38. Cystic fibrosis in Korean children:a case report identified by a quantitative pilocarpine iontophoresis sweat test and genetic analysis.
    Ahn KM, Park HY, Lee JH, Lee MG, Kim JH, Kang IJ, Lee SI.
    J Korean Med Sci; 2005 Feb 01; 20(1):153-7. PubMed ID: 15716623
    [Abstract] [Full Text] [Related]

  • 39. [Aquagenic palmoplantar keratoderma in children with cystic fibrosis].
    Weil B, Chaillou E, Troussier F, Pelatan C, Chiffoleau M, Darviot E, Chevalier MC, Martin L, Giniès JL.
    Arch Pediatr; 2013 Dec 01; 20(12):1306-9. PubMed ID: 24210985
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  • 40. Distribution of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mutations in a Cohort of Patients Residing in Palestine.
    Siryani I, Jama M, Rumman N, Marzouqa H, Kannan M, Lyon E, Hindiyeh M.
    PLoS One; 2015 Dec 01; 10(7):e0133890. PubMed ID: 26208274
    [Abstract] [Full Text] [Related]

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