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PUBMED FOR HANDHELDS

Journal Abstract Search


137 related items for PubMed ID: 16177157

  • 1.
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  • 2. Growth in prepubertal children with cystic fibrosis, homozygous for the Delta F508 mutation.
    Keller BM, Aebischer CC, Kraemer R, Schöni MH.
    J Cyst Fibros; 2003 Jun; 2(2):76-83. PubMed ID: 15463854
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  • 3. Clinical outcome of cystic fibrosis presenting with or without meconium ileus: a matched cohort study.
    Munck A, Gérardin M, Alberti C, Ajzenman C, Lebourgeois M, Aigrain Y, Navarro J.
    J Pediatr Surg; 2006 Sep; 41(9):1556-60. PubMed ID: 16952591
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  • 5. Achromobacter xylosoxidans in cystic fibrosis: prevalence and clinical relevance.
    De Baets F, Schelstraete P, Van Daele S, Haerynck F, Vaneechoutte M.
    J Cyst Fibros; 2007 Jan; 6(1):75-8. PubMed ID: 16793350
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  • 7. Modifier effect of the Toll-like receptor 4 D299G polymorphism in children with cystic fibrosis.
    Urquhart DS, Allen J, Elrayess M, Fidler K, Klein N, Jaffé A.
    Arch Immunol Ther Exp (Warsz); 2006 Jan; 54(4):271-6. PubMed ID: 16830219
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  • 8. Cystic fibrosis diagnosed after 2 months of age leads to worse outcomes and requires more therapy.
    Sims EJ, Clark A, McCormick J, Mehta G, Connett G, Mehta A, United Kingdom Cystic Fibrosis Database Steering Committee.
    Pediatrics; 2007 Jan; 119(1):19-28. PubMed ID: 17200267
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  • 10. Does presenting with meconium ileus affect the prognosis of children with cystic fibrosis?
    Johnson JA, Bush A, Buchdahl R.
    Pediatr Pulmonol; 2010 Oct; 45(10):951-8. PubMed ID: 20672292
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  • 11. Association of mannose-binding lectin gene heterogeneity with severity of lung disease and survival in cystic fibrosis.
    Garred P, Pressler T, Madsen HO, Frederiksen B, Svejgaard A, Høiby N, Schwartz M, Koch C.
    J Clin Invest; 1999 Aug; 104(4):431-7. PubMed ID: 10449435
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  • 12. Comparing the clinical evolution of cystic fibrosis screened neonatally to that of cystic fibrosis diagnosed from clinical symptoms: a 10-year retrospective study in a French region (Brittany).
    Siret D, Bretaudeau G, Branger B, Dabadie A, Dagorne M, David V, de Braekeleer M, Moisan-Petit V, Picherot G, Rault G, Storni V, Roussey M.
    Pediatr Pulmonol; 2003 May; 35(5):342-9. PubMed ID: 12687590
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  • 13. Association of body composition and lung function in children with cystic fibrosis.
    Pedreira CC, Robert RG, Dalton V, Oliver MR, Carlin JB, Robinson P, Cameron FJ.
    Pediatr Pulmonol; 2005 Mar; 39(3):276-80. PubMed ID: 15668934
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  • 15. Changes in lung function in young cystic fibrosis patients between two courses of intravenous antibiotics against Pseudomonas aeruginosa.
    Béghin L, Michaud L, Loeuille GA, Wizla-Derambure N, Sayah H, Sardet A, Thumerelle C, Deschildre A, Turck D, Gottrand F.
    Pediatr Pulmonol; 2009 May; 44(5):464-71. PubMed ID: 19360849
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  • 17. Growth assessment of paediatric patients with CF comparing different auxologic indicators: A multicentre Italian study.
    Lucidi V, Alghisi F, Raia V, Russo B, Valmarana L, Valmarana R, Coruzzo A, Beschi S, Dester S, Rinaldi D, Maglieri M, Guidotti ML, Ravaioli E, Pesola M, De Alessandri A, Padoan R, Grynzich L, Ratclif L, Repetto T, Ambroni M, Provenzano E, Tozzi AE, Colombo C.
    J Pediatr Gastroenterol Nutr; 2009 Sep; 49(3):335-42. PubMed ID: 19543116
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  • 18. Nutritional intake and status in children with cystic fibrosis: does age matter?
    White H, Wolfe SP, Foy J, Morton A, Conway SP, Brownlee KB.
    J Pediatr Gastroenterol Nutr; 2007 Jan; 44(1):116-23. PubMed ID: 17204964
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  • 19. 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
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  • 20. Adolescent development and energy expenditure in females with cystic fibrosis.
    Stallings VA, Tomezsko JL, Schall JI, Mascarenhas MR, Stettler N, Scanlin TF, Zemel BS.
    Clin Nutr; 2005 Oct; 24(5):737-45. PubMed ID: 16182037
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