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Journal Abstract Search

390 related items for PubMed ID: 20503286

  • 1. Long-term effects of birth order and age at diagnosis in cystic fibrosis: a sibling cohort study.
    Slieker MG, van den Berg JM, Kouwenberg J, van Berkhout FT, Heijerman HG, van der Ent CK.
    Pediatr Pulmonol; 2010 Jun; 45(6):601-7. PubMed ID: 20503286
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  • 2. 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; 38(4):292-7. PubMed ID: 15334505
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  • 3. Disease severity in siblings with cystic fibrosis.
    Katz SL, Strug LJ, Coates AL, Corey M.
    Pediatr Pulmonol; 2004 May; 37(5):407-12. PubMed ID: 15095323
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  • 5. Baseline characteristics and factors associated with nutritional and pulmonary status at enrollment in the cystic fibrosis EPIC observational cohort.
    Rosenfeld M, Emerson J, McNamara S, Joubran K, Retsch-Bogart G, Graff GR, Gutierrez HH, Kanga JF, Lahiri T, Noyes B, Ramsey B, Ren CL, Schechter M, Morgan W, Gibson RL, EPIC Study Group Participating Clinical Sites.
    Pediatr Pulmonol; 2010 Sep; 45(9):934-44. PubMed ID: 20597081
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  • 6. 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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  • 7. Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype.
    De Boeck K, Weren M, Proesmans M, Kerem E.
    Pediatrics; 2005 Apr; 115(4):e463-9. PubMed ID: 15772171
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  • 10. The importance of sweat testing for older siblings of patients with cystic fibrosis identified by newborn screening.
    Munck A, Houssin E, Roussey M.
    J Pediatr; 2009 Dec; 155(6):928-930.e1. PubMed ID: 19914431
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  • 11. Non-classic cystic fibrosis associated with D1152H CFTR mutation.
    Burgel PR, Fajac I, Hubert D, Grenet D, Stremler N, Roussey M, Siret D, Languepin J, Mely L, Fanton A, Labbé A, Domblides P, Vic P, Dagorne M, Reynaud-Gaubert M, Counil F, Varaigne F, Bienvenu T, Bellis G, Dusser D.
    Clin Genet; 2010 Apr; 77(4):355-64. PubMed ID: 19843100
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  • 12. 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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  • 13. 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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  • 17. Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis.
    Nixon GM, Armstrong DS, Carzino R, Carlin JB, Olinsky A, Robertson CF, Grimwood K.
    J Pediatr; 2001 May; 138(5):699-704. PubMed ID: 11343046
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  • 18. Long-term pulmonary outcome after meconium ileus in cystic fibrosis.
    Kappler M, Feilcke M, Schröter C, Kraxner A, Griese M.
    Pediatr Pulmonol; 2009 Dec; 44(12):1201-6. PubMed ID: 19911366
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  • 19. Infant care patterns at epidemiologic study of cystic fibrosis sites that achieve superior childhood lung function.
    Padman R, McColley SA, Miller DP, Konstan MW, Morgan WJ, Schechter MS, Ren CL, Wagener JS, Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis.
    Pediatrics; 2007 Mar; 119(3):e531-7. PubMed ID: 17332172
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  • 20. Neonatal screening for cystic fibrosis: long-term clinical balance.
    Mastella G, Zanolla L, Castellani C, Altieri S, Furnari M, Giglio L, Lombardo M, Miano A, Sciuto C, Pardo F, Magazzù G.
    Pancreatology; 2001 Mar; 1(5):531-7. PubMed ID: 12120233
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