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Journal Abstract Search

294 related items for PubMed ID: 24249707

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  • 2. 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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  • 4. 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; 65(7):594-9. PubMed ID: 20627915
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  • 5. 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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  • 6. Cystic fibrosis: need for mass deployable screening methods.
    Sengar AS, Agarwal A, Singh MK.
    Appl Biochem Biotechnol; 2014 Oct 01; 174(3):1127-36. PubMed ID: 24880895
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  • 8. A simplified cyclic adenosine monophosphate-mediated sweat rate test for quantitative measure of cystic fibrosis transmembrane regulator (CFTR) function.
    Callen A, Diener-West M, Zeitlin PL, Rubenstein RC.
    J Pediatr; 2000 Dec 01; 137(6):849-55. PubMed ID: 11113843
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  • 10. Sweat Proteomics in Cystic Fibrosis: Discovering Companion Biomarkers for Precision Medicine and Therapeutic Development.
    Burat B, Reynaerts A, Baiwir D, Fléron M, Gohy S, Eppe G, Leal T, Mazzucchelli G.
    Cells; 2022 Jul 31; 11(15):. PubMed ID: 35954202
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  • 12. Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis.
    Goubau C, Wilschanski M, Skalická V, Lebecque P, Southern KW, Sermet I, Munck A, Derichs N, Middleton PG, Hjelte L, Padoan R, Vasar M, De Boeck K.
    Thorax; 2009 Aug 31; 64(8):683-91. PubMed ID: 19318346
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  • 17. Diagnosis of cystic fibrosis by sweat testing: age-specific reference intervals.
    Mishra A, Greaves R, Smith K, Carlin JB, Wootton A, Stirling R, Massie J.
    J Pediatr; 2008 Dec 31; 153(6):758-63. PubMed ID: 18589442
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  • 18. Iontophoretic beta-adrenergic stimulation of human sweat glands: possible assay for cystic fibrosis transmembrane conductance regulator activity in vivo.
    Shamsuddin AK, Reddy MM, Quinton PM.
    Exp Physiol; 2008 Aug 31; 93(8):969-81. PubMed ID: 18441335
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  • 19. [Comparison of the classical Gibson-Cooke methods and the chloride-sensitive electrode in sweat testing for diagnosis of cystic fibrosis].
    Riedler J, Arrer E.
    Padiatr Padol; 1991 Aug 31; 26(4):173-5. PubMed ID: 1749624
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  • 20. 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 31; 51():345-8. PubMed ID: 12723646
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