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Journal Abstract Search

960 related items for PubMed ID: 15930234

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  • 24. 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
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  • 25. Delayed diagnosis of cystic fibrosis and the family perspective.
    Kharrazi M, Kharrazi LD.
    J Pediatr; 2005 Sep; 147(3 Suppl):S21-5. PubMed ID: 16202777
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  • 27. Cystic fibrosis detection in high-risk Egyptian children and CFTR mutation analysis.
    Naguib ML, Schrijver I, Gardner P, Pique LM, Doss SS, Abu Zekry MA, Aziz M, Nasr SZ.
    J Cyst Fibros; 2007 Apr; 6(2):111-6. PubMed ID: 16837250
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  • 28. Implementation of informed consent for a cystic fibrosis newborn screening program in France: low refusal rates for optional testing.
    Dhondt JL.
    J Pediatr; 2005 Sep; 147(3 Suppl):S106-8. PubMed ID: 16202772
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  • 29. Diagnosis of cystic fibrosis after newborn screening: the Australasian experience--twenty years and five million babies later: a consensus statement from the Australasian Paediatric Respiratory Group.
    Massie J, Clements B, Australian Paediatric Respiratory Group.
    Pediatr Pulmonol; 2005 May; 39(5):440-6. PubMed ID: 15704202
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  • 31. A sweat test centered protocol for the disclosure and diagnosis of cystic fibrosis in a newborn screening program.
    Doull IJ, Hall SJ, Bradley DM.
    Pediatr Pulmonol; 2007 Sep; 42(9):773-8. PubMed ID: 17659601
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  • 36. Emerging issues in cystic fibrosis newborn screening.
    Castellani C, Massie J.
    Curr Opin Pulm Med; 2010 Nov; 16(6):584-90. PubMed ID: 20814308
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  • 39. 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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