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PUBMED FOR HANDHELDS

Journal Abstract Search


144 related items for PubMed ID: 25667564

  • 1. 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; 2015():306825. PubMed ID: 25667564
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  • 2. The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening.
    Sermet-Gaudelus I, Roussel D, Bui S, Deneuville E, Huet F, Reix P, Bellon G, Lenoir G, Edelman A.
    BMC Pediatr; 2006 Oct 03; 6():25. PubMed ID: 17018149
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  • 3. 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 03; 65(6):539-44. PubMed ID: 20522854
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  • 4. 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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  • 7. 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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  • 11. Nasal potential difference outcomes support diagnostic decisions in cystic fibrosis.
    Tridello G, Menin L, Pintani E, Bergamini G, Assael BM, Melotti P.
    J Cyst Fibros; 2016 Sep 01; 15(5):579-82. PubMed ID: 27423539
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  • 15. Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis.
    Bienvenu T, Sermet-Gaudelus I, Burgel PR, Hubert D, Crestani B, Bassinet L, Dusser D, Fajac I.
    Am J Respir Crit Care Med; 2010 May 15; 181(10):1078-84. PubMed ID: 20167849
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  • 17. Relevance of nasal potential difference in diagnosis of cystic fibrosis among children.
    Valiulis A, Skurvydienė I, Misevičienė V, Kasnauskienė J, Vaidelienė L, Utkus A.
    Medicina (Kaunas); 2013 May 15; 49(4):185-90. PubMed ID: 23985983
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  • 19. 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 15; 65(7):594-9. PubMed ID: 20627915
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