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Volumn 24, Issue , 2017, Pages 32-34

Ataluren and similar compounds (specific therapies for premature termination codon class I mutations) for cystic fibrosis

Author keywords

[No Author keywords available]

Indexed keywords

ATALUREN; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; OXADIAZOLE DERIVATIVE;

EID: 85019899702     PISSN: 15260542     EISSN: 15260550     Source Type: Journal    
DOI: 10.1016/j.prrv.2017.04.001     Document Type: Article
Times cited : (8)

References (7)
  • 1
    • 85011252770 scopus 로고    scopus 로고
    • Ataluren and similar compounds (specific therapies for premature termination codon class I mutations) for cystic fibrosis
    • Art. No.: CD012040
    • Aslam, A.A., Higgins, C., Sinha, I.P., Southern, K.W., Ataluren and similar compounds (specific therapies for premature termination codon class I mutations) for cystic fibrosis. Cochrane Database of Systematic Reviews(1), 2017, 10.1002/14651858.CD012040.pub2 Art. No.: CD012040.
    • (2017) Cochrane Database of Systematic Reviews , Issue.1
    • Aslam, A.A.1    Higgins, C.2    Sinha, I.P.3    Southern, K.W.4
  • 3
    • 85029717072 scopus 로고    scopus 로고
    • Cystic Fibrosis Centre at the Hospital for Sick Children in Toronto, Canada. Cystic Fibrosis Mutation Database. (accessed 15.03.2015).
    • Cystic Fibrosis Centre at the Hospital for Sick Children in Toronto, Canada. Cystic Fibrosis Mutation Database. www.genet.sickkids.on.ca/StatisticsPage.html (accessed 15.03.2015).
  • 4
    • 84904016376 scopus 로고    scopus 로고
    • Ataluren for the treatment of nonsense-mutation cystic fibrosis: a randomised, double-blind, placebo-controlled phase 3 trial
    • Kerem, E., Konstan, M.W., De Boeck, K., Accurso, F.J., Sermet-Gaudelus, I., Wilschanski, M., et al. Ataluren for the treatment of nonsense-mutation cystic fibrosis: a randomised, double-blind, placebo-controlled phase 3 trial. The Lancet. Respiratory Medicine 2:7 (2014), 539–547.
    • (2014) The Lancet. Respiratory Medicine , vol.2 , Issue.7 , pp. 539-547
    • Kerem, E.1    Konstan, M.W.2    De Boeck, K.3    Accurso, F.J.4    Sermet-Gaudelus, I.5    Wilschanski, M.6
  • 5
    • 85029678394 scopus 로고    scopus 로고
    • Sterne JAC on behalf of the Cochrane Statistical Methods Group and the Cochrane Bias Methods Group editor(s). Chapter 8: Assessing risk of bias in included studies. In: Higgins JPT, Green S editor(s). Cochrane Handbook for Systematic Reviews of Interventions Version 5.1 (updated March 2011). The Cochrane Collaboration,, Available from
    • Higgins JPT, Altman DG, Sterne JAC on behalf of the Cochrane Statistical Methods Group and the Cochrane Bias Methods Group editor(s). Chapter 8: Assessing risk of bias in included studies. In: Higgins JPT, Green S editor(s). Cochrane Handbook for Systematic Reviews of Interventions Version 5.1 (updated March 2011). The Cochrane Collaboration, 2011. Available from handbook.cochrane.org/.
    • (2011)
    • Higgins, J.P.T.1    Altman, D.G.2
  • 6
    • 85029715535 scopus 로고    scopus 로고
    • Guyatt GH on behalf of the Cochrane Applicability and Recommendations Methods Group and the Cochrane Statistical Methods Group. Chapter 11: Presenting results and ‘Summary of findings’ tables. In: Higgins JPT, Green S (editors). Cochrane Handbook for Systematic Reviews of Interventions Version 5.1 (updated March 2011). The Cochrane Collaboration,, Available from
    • Schünemann HJ, Oxman AD, Higgins JPT, Vist GE, Glasziou P, Guyatt GH on behalf of the Cochrane Applicability and Recommendations Methods Group and the Cochrane Statistical Methods Group. Chapter 11: Presenting results and ‘Summary of findings’ tables. In: Higgins JPT, Green S (editors). Cochrane Handbook for Systematic Reviews of Interventions Version 5.1 (updated March 2011). The Cochrane Collaboration, 2011. Available from handbook.cochrane.org/.
    • (2011)
    • Schünemann, H.J.1    Oxman, A.D.2    Higgins, J.P.T.3    Vist, G.E.4    Glasziou, P.5
  • 7
    • 85029693362 scopus 로고    scopus 로고
    • ®) in patients with nonsense mutation cystic fibrosis
    • ®) in patients with nonsense mutation cystic fibrosis. https://clinicaltrials.gov/ct2/show/NCT02139306.
    • McIntosh, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.