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Volumn 67, Issue 6, 2012, Pages 471-472

'To CT or not to CT? That is the question': Outcome surrogates for surveillance in childhood cystic fibrosis

Author keywords

[No Author keywords available]

Indexed keywords

TRANSMEMBRANE CONDUCTANCE REGULATOR;

EID: 84861907602     PISSN: 00406376     EISSN: 14683296     Source Type: Journal    
DOI: 10.1136/thoraxjnl-2011-201549     Document Type: Editorial
Times cited : (3)

References (12)
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    • (2012) Thorax , vol.67 , pp. 509-516
    • Mott, L.S.1    Park, J.2    Murray, C.P.3
  • 3
    • 79956360940 scopus 로고    scopus 로고
    • Lung clearance index and HRCT are complementary markers of lung abnormalities in young children with CF
    • Owens CM, Aurora P, Stanojevic S, et al. Lung clearance index and HRCT are complementary markers of lung abnormalities in young children with CF. Thorax 2011;66:481-8.
    • (2011) Thorax , vol.66 , pp. 481-488
    • Owens, C.M.1    Aurora, P.2    Stanojevic, S.3
  • 4
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    • 78650016662 scopus 로고    scopus 로고
    • Sensitivity of lung clearance index and chest CT in early CF lung disease
    • Ellemunter H, Fuchs SI, Unsinn KM, et al. Sensitivity of lung clearance index and chest CT in early CF lung disease. Respir Med 2010;104:1834-42.
    • (2010) Respir Med , vol.104 , pp. 1834-1842
    • Ellemunter, H.1    Fuchs, S.I.2    Unsinn, K.M.3
  • 7
    • 70449434777 scopus 로고    scopus 로고
    • Cancer risk among patients with cystic fibrosis and their first degree relatives
    • Johannesson M, Askling J, Montgomery SM, et al. Cancer risk among patients with cystic fibrosis and their first degree relatives. Int J Cancer 2009;125:2953-6.
    • (2009) Int J Cancer , vol.125 , pp. 2953-2956
    • Johannesson, M.1    Askling, J.2    Montgomery, S.M.3
  • 9
    • 80455162465 scopus 로고    scopus 로고
    • A CFTR potentiator in patients with CF and the G551D mutation
    • Ramsey BW, Davies J, McElvaney NG, et al. A CFTR potentiator in patients with CF and the G551D mutation. N Engl J Med 2011;365:1663-72.
    • (2011) N Engl J Med , vol.365 , pp. 1663-1672
    • Ramsey, B.W.1    Davies, J.2    McElvaney, N.G.3
  • 10
    • 84855202429 scopus 로고    scopus 로고
    • Results of a phase IIa study VX-809, an investigational CFRT corrector compound, in subjects with CF homozygous for the F508del-CFTR mutation
    • Clancy JP, Rowe SM, Accurso FJ, et al. Results of a phase IIa study VX-809, an investigational CFRT corrector compound, in subjects with CF homozygous for the F508del-CFTR mutation. Thorax 2012;67:12-18.
    • (2012) Thorax , vol.67 , pp. 12-18
    • Clancy, J.P.1    Rowe, S.M.2    Accurso, F.J.3
  • 11
    • 70350508400 scopus 로고    scopus 로고
    • Cystic fibrosis: Are volumetric ultra-low-dose expiratory CT scans sufficient for monitoring related lung disease?
    • Loeve M, Lequin MH, de Bruijne M, et al. Cystic fibrosis: are volumetric ultra-low-dose expiratory CT scans sufficient for monitoring related lung disease? Radiology 2009;253:223-9.
    • (2009) Radiology , vol.253 , pp. 223-229
    • Loeve, M.1    Lequin, M.H.2    De Bruijne, M.3
  • 12
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    • Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis
    • DOI 10.1136/thx.2007.077784
    • Gustaffson PM, De Jong PA, Tiddens HA. Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis. Thorax 2008;63:129-34. (Pubitemid 351236476)
    • (2008) Thorax , vol.63 , Issue.2 , pp. 129-134
    • Gustafsson, P.M.1    De Jong, P.A.2    Tiddens, H.A.W.M.3    Lindblad, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.