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136 related items for PubMed ID: 21449922

  • 21. Pseudo-Bartter's Syndrome in Patients with Cystic Fibrosis: A Case Series and Review of the Literature.
    Vilotijević-Dautović G, Stojanović V.
    Srp Arh Celok Lek; 2015; 143(11-12):748-51. PubMed ID: 26946774
    [Abstract] [Full Text] [Related]

  • 22. Clinical outcomes in infants with cystic fibrosis transmembrane conductance regulator (CFTR) related metabolic syndrome.
    Ren CL, Desai H, Platt M, Dixon M.
    Pediatr Pulmonol; 2011 Nov; 46(11):1079-84. PubMed ID: 21538969
    [Abstract] [Full Text] [Related]

  • 23. Early aggressive eradication therapy for intermittent Pseudomonas aeruginosa airway colonization in cystic fibrosis patients: 15 years experience.
    Hansen CR, Pressler T, Høiby N.
    J Cyst Fibros; 2008 Nov; 7(6):523-30. PubMed ID: 18693078
    [Abstract] [Full Text] [Related]

  • 24. [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
    [Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. Longitudinal assessment of Pseudomonas aeruginosa in young children with cystic fibrosis.
    Burns JL, Gibson RL, McNamara S, Yim D, Emerson J, Rosenfeld M, Hiatt P, McCoy K, Castile R, Smith AL, Ramsey BW.
    J Infect Dis; 2001 Feb 01; 183(3):444-52. PubMed ID: 11133376
    [Abstract] [Full Text] [Related]

  • 27. Emergence and persistence of Pseudomonas aeruginosa in the cystic fibrosis airway.
    Fick RB, Sonoda F, Hornick DB.
    Semin Respir Infect; 1992 Sep 01; 7(3):168-78. PubMed ID: 1475541
    [Abstract] [Full Text] [Related]

  • 28. Strategies of Pseudomonas aeruginosa to colonize and to persist in the cystic fibrosis lung.
    Kubesch P, Lingner M, Grothues D, Wehsling M, Tümmler B.
    Scand J Gastroenterol Suppl; 1988 Sep 01; 143():77-80. PubMed ID: 3133755
    [Abstract] [Full Text] [Related]

  • 29. Relationship between cystic fibrosis respiratory tract bacterial communities and age, genotype, antibiotics and Pseudomonas aeruginosa.
    Klepac-Ceraj V, Lemon KP, Martin TR, Allgaier M, Kembel SW, Knapp AA, Lory S, Brodie EL, Lynch SV, Bohannan BJ, Green JL, Maurer BA, Kolter R.
    Environ Microbiol; 2010 May 01; 12(5):1293-303. PubMed ID: 20192960
    [Abstract] [Full Text] [Related]

  • 30. Diverse genotypical features and impacts on clinical course and severity of cystic fibrosis: early childhood experience.
    Halicioglu O, Akman SA, Sutcuoglu S, Coker I.
    Minerva Pediatr; 2011 Jun 01; 63(3):169-75. PubMed ID: 21654597
    [Abstract] [Full Text] [Related]

  • 31. Severe episodes of extra cellular dehydration: an atypical adult presentation of cystic fibrosis.
    Augusto JF, Sayegh J, Malinge MC, Illouz F, Subra JF, Ducluzeau PH.
    Clin Nephrol; 2008 Apr 01; 69(4):302-5. PubMed ID: 18397707
    [Abstract] [Full Text] [Related]

  • 32. A novel exon duplication of the cystic fibrosis transmembrane conductance regulator in a patient presenting with adult-onset recurrent pancreatitis.
    Kopp BT, Pastore MT, Sturm AC, Holtzlander MJ, Westman JA.
    Pancreas; 2011 Jul 01; 40(5):773-7. PubMed ID: 21673536
    [Abstract] [Full Text] [Related]

  • 33. Cystic fibrosis in Saudi Arabia: common and rare presentations.
    Al-Mobaireek KF, Abdullah AM.
    Ann Trop Paediatr; 1995 Dec 01; 15(4):269-72. PubMed ID: 8687200
    [Abstract] [Full Text] [Related]

  • 34. Familial concordance of phenotype and microbial variation among siblings with CF.
    Picard E, Aviram M, Yahav Y, Rivlin J, Blau H, Bentur L, Avital A, Villa Y, Schwartz S, Kerem B, Kerem E.
    Pediatr Pulmonol; 2004 Oct 01; 38(4):292-7. PubMed ID: 15334505
    [Abstract] [Full Text] [Related]

  • 35. Pathophysiology and management of pulmonary infections in cystic fibrosis.
    Gibson RL, Burns JL, Ramsey BW.
    Am J Respir Crit Care Med; 2003 Oct 15; 168(8):918-51. PubMed ID: 14555458
    [Abstract] [Full Text] [Related]

  • 36. Identification of a novel mutation of CFTR gene in a Korean patient with cystic fibrosis.
    Ko JM, Kim GH, Kim KM, Hong SJ, Yoo HW.
    J Korean Med Sci; 2008 Oct 15; 23(5):912-5. PubMed ID: 18955805
    [Abstract] [Full Text] [Related]

  • 37. [Isolated pathogen microorganisms in respiratory samples from children with cystic fibrosis].
    Anzaudo MM, Busquets NP, Ronchi S, Mayoral C.
    Rev Argent Microbiol; 2005 Oct 15; 37(3):129-34. PubMed ID: 16323660
    [Abstract] [Full Text] [Related]

  • 38. [Cystic fibrosis primarily presenting with pseudo-Bartter syndrome: a report of three cases and literature review].
    Zhang JY, Sun LJ, Duan XJ, Zhang ZM, Xiao ZH, Chen YP, You JY.
    Zhongguo Dang Dai Er Ke Za Zhi; 2024 May 15; 26(5):506-511. PubMed ID: 38802912
    [Abstract] [Full Text] [Related]

  • 39. [Cystic fibrosis revealed by dehydration with hypochloronatremic alkalosis in 3 infants and a neonate].
    Bérard E, Maillotte AM, Albertini M, Delalandre E, Boutté P, Mariani R.
    Arch Pediatr; 1994 Jan 15; 1(1):42-5. PubMed ID: 8087218
    [Abstract] [Full Text] [Related]

  • 40. Association of beta-defensin-1 gene polymorphisms with Pseudomonas aeruginosa airway colonization in cystic fibrosis.
    Tesse R, Cardinale F, Santostasi T, Polizzi A, Manca A, Mappa L, Iacoviello G, De Robertis F, Logrillo VP, Armenio L.
    Genes Immun; 2008 Jan 15; 9(1):57-60. PubMed ID: 17960157
    [Abstract] [Full Text] [Related]

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