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Journal Abstract Search

459 related items for PubMed ID: 7472820

  • 21. [Cystic fibrosis and normal sweat chloride values: a case-report].
    Lebecque P, Leal T, Godding V.
    Rev Mal Respir; 2001 Sep; 18(4 Pt 1):443-5. PubMed ID: 11547256
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  • 22. Refining the continuum of CFTR-associated disorders in the era of newborn screening.
    Levy H, Nugent M, Schneck K, Stachiw-Hietpas D, Laxova A, Lakser O, Rock M, Dahmer MK, Biller J, Nasr SZ, Baker M, McColley SA, Simpson P, Farrell PM.
    Clin Genet; 2016 May; 89(5):539-49. PubMed ID: 26671754
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  • 27. A multicenter evaluation of sweat chloride concentration and variation in infants with cystic fibrosis.
    LeGrys VA, Moon TC, Laux J, Accurso F, Martiniano SA.
    J Cyst Fibros; 2019 Mar; 18(2):190-193. PubMed ID: 30583934
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  • 28. Mutations in the cystic fibrosis transmembrane regulator gene and in vivo transepithelial potentials.
    Wilschanski M, Dupuis A, Ellis L, Jarvi K, Zielenski J, Tullis E, Martin S, Corey M, Tsui LC, Durie P.
    Am J Respir Crit Care Med; 2006 Oct 01; 174(7):787-94. PubMed ID: 16840743
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  • 29. Genotype-phenotype correlation and functional studies in patients with cystic fibrosis bearing CFTR complex alleles.
    Terlizzi V, Castaldo G, Salvatore D, Lucarelli M, Raia V, Angioni A, Carnovale V, Cirilli N, Casciaro R, Colombo C, Di Lullo AM, Elce A, Iacotucci P, Comegna M, Scorza M, Lucidi V, Perfetti A, Cimino R, Quattrucci S, Seia M, Sofia VM, Zarrilli F, Amato F.
    J Med Genet; 2017 Apr 01; 54(4):224-235. PubMed ID: 27738188
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  • 35. Variability of sweat chloride concentration in subjects with cystic fibrosis and G551D mutations.
    Vermeulen F, Le Camus C, Davies JC, Bilton D, Milenković D, De Boeck K.
    J Cyst Fibros; 2017 Jan 01; 16(1):36-40. PubMed ID: 26996268
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  • 37. 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 01; 52(4):472-479. PubMed ID: 28068001
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  • 38. Screening for cystic fibrosis: the importance of using the correct tools.
    Shah U, Moatter T.
    J Ayub Med Coll Abbottabad; 2006 Apr 01; 18(1):7-10. PubMed ID: 16773960
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  • 39. Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport.
    Sermet-Gaudelus I, Girodon E, Sands D, Stremmler N, Vavrova V, Deneuville E, Reix P, Bui S, Huet F, Lebourgeois M, Munck A, Iron A, Skalicka V, Bienvenu T, Roussel D, Lenoir G, Bellon G, Sarles J, Macek M, Roussey M, Fajac I, Edelman A.
    Am J Respir Crit Care Med; 2010 Oct 01; 182(7):929-36. PubMed ID: 20538955
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  • 40. Cystic Fibrosis Gene Mutation Frequency Among a Group of Suspected Children in King Hussein Medical Center.
    Al-Abadi B, Al-Hiary M, Khasawneh R, Al-Momani A, Bani-Salameh A, Al-Saeidat S, Al-Khlaifat A, Aboalsondos O.
    Med Arch; 2019 Apr 01; 73(2):118-120. PubMed ID: 31391700
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