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Journal Abstract Search

327 related items for PubMed ID: 26996268

  • 61. Borderline sweat test: Utility and limits of genetic analysis for the diagnosis of cystic fibrosis.
    Seia M, Costantino L, Paracchini V, Porcaro L, Capasso P, Coviello D, Corbetta C, Torresani E, Magazzù D, Consalvo V, Monti A, Costantini D, Colombo C.
    Clin Biochem; 2009 May; 42(7-8):611-6. PubMed ID: 19318035
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  • 62. Molecular diagnosis of cystic fibrosis in Indian patients--a preliminary report.
    Ashavaid TF, Dherai AJ, Kondkar AA, Raghavan R, Udani SV, Udwadia ZF, Desai D.
    J Assoc Physicians India; 2003 Apr; 51():345-8. PubMed ID: 12723646
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  • 63. Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations.
    Wilschanski M, Zielenski J, Markiewicz D, Tsui LC, Corey M, Levison H, Durie PR.
    J Pediatr; 1995 Nov; 127(5):705-10. PubMed ID: 7472820
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  • 64. 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; 64(11):932-8. PubMed ID: 19734129
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  • 65. A mutation in the cystic fibrosis transmembrane conductance regulator gene associated with elevated sweat chloride concentrations in the absence of cystic fibrosis.
    Mickle JE, Macek M, Fulmer-Smentek SB, Egan MM, Schwiebert E, Guggino W, Moss R, Cutting GR.
    Hum Mol Genet; 1998 Apr; 7(4):729-35. PubMed ID: 9499426
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  • 66. The magnitude of ivacaftor effects on fluid secretion via R117H-CFTR channels: Human in vivo measurements.
    Char JE, Dunn C, Davies Z, Milla C, Moss RB, Wine JJ.
    PLoS One; 2017 Apr; 12(4):e0175486. PubMed ID: 28419121
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  • 67. Overexpression of RANK and M-CSFR in Monocytes of G551D-Bearing Patients with Cystic Fibrosis.
    Velard F, Jourdain ML, Abdallah D, Jacquot J, Ronan N, McCarthy Y, Flanagan E, Plant B.
    Am J Respir Crit Care Med; 2018 Oct 01; 198(7):968-970. PubMed ID: 29940131
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  • 73. [Cystic fibrosis and normal sweat chloride values: a case-report].
    Lebecque P, Leal T, Godding V.
    Rev Mal Respir; 2001 Sep 01; 18(4 Pt 1):443-5. PubMed ID: 11547256
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  • 74. Mutations of the cystic fibrosis gene and intermediate sweat chloride levels in children.
    Lebecque P, Leal T, De Boeck C, Jaspers M, Cuppens H, Cassiman JJ.
    Am J Respir Crit Care Med; 2002 Mar 15; 165(6):757-61. PubMed ID: 11897640
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  • 76. Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR.
    Wainwright CE, Elborn JS, Ramsey BW, Marigowda G, Huang X, Cipolli M, Colombo C, Davies JC, De Boeck K, Flume PA, Konstan MW, McColley SA, McCoy K, McKone EF, Munck A, Ratjen F, Rowe SM, Waltz D, Boyle MP, TRAFFIC Study Group, TRANSPORT Study Group.
    N Engl J Med; 2015 Jul 16; 373(3):220-31. PubMed ID: 25981758
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  • 80. 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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