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Volumn 72, Issue 8, 2017, Pages 760-762

Detection of early subclinical lung disease in children with cystic fibrosis by lung ventilation imaging with hyperpolarised gas MRI

Author keywords

Cystic Fibrosis; Imaging CT MRI etc; Respiratory Measurement

Indexed keywords

HELIUM; HYDROGEN;

EID: 85021219355     PISSN: 00406376     EISSN: 14683296     Source Type: Journal    
DOI: 10.1136/thoraxjnl-2016-208948     Document Type: Letter
Times cited : (73)

References (10)
  • 1
    • 39049105720 scopus 로고    scopus 로고
    • Lung clearance index is a sensitive, repeatable and practical measure of airways disease in adults with cystic fibrosis
    • Horsley AR, Gustafsson PM, Macleod KA, et al. Lung clearance index is a sensitive, repeatable and practical measure of airways disease in adults with cystic fibrosis. Thorax 2008;63:135-40.
    • (2008) Thorax , vol.63 , pp. 135-140
    • Horsley, A.R.1    Gustafsson, P.M.2    Macleod, K.A.3
  • 2
    • 77950396804 scopus 로고    scopus 로고
    • Hyperpolarized 3He MR for sensitive imaging of ventilation function and treatment efficiency in young cystic fibrosis patients with normal lung function
    • Bannier E, Cieslar K, Mosbah K, et al. Hyperpolarized 3He MR for sensitive imaging of ventilation function and treatment efficiency in young cystic fibrosis patients with normal lung function. Radiology 2010;255:225-32.
    • (2010) Radiology , vol.255 , pp. 225-232
    • Bannier, E.1    Cieslar, K.2    Mosbah, K.3
  • 3
    • 0347766074 scopus 로고    scopus 로고
    • Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis
    • de Jong PA, Nakano Y, Lequin MH, et al. Progressive damage on high resolution computed tomography despite stable lung function in cystic fibrosis. Eur Respir J 2004;23:93-7.
    • (2004) Eur Respir J , vol.23 , pp. 93-97
    • De Jong, P.A.1    Nakano, Y.2    Lequin, M.H.3
  • 4
    • 84943776255 scopus 로고    scopus 로고
    • Ventilation heterogeneity and the benefits and challenges of multiple breath washout testing in patients with cystic fibrosis
    • Horsley A, Wild JM. Ventilation heterogeneity and the benefits and challenges of multiple breath washout testing in patients with cystic fibrosis. Paediatr Respir Rev 2015;16(Suppl 1):15-18.
    • (2015) Paediatr Respir Rev , vol.16 , pp. 15-18
    • Horsley, A.1    Wild, J.M.2
  • 5
    • 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
  • 6
    • 0346121620 scopus 로고    scopus 로고
    • Evaluation of ventilation maldistribution as an early indicator of lung disease in children with cystic fibrosis
    • Gustafsson PM, Aurora P, Lindblad A. Evaluation of ventilation maldistribution as an early indicator of lung disease in children with cystic fibrosis. Eur Respir J 2003;22:972-9.
    • (2003) Eur Respir J , vol.22 , pp. 972-979
    • Gustafsson, P.M.1    Aurora, P.2    Lindblad, A.3
  • 7
    • 50849128461 scopus 로고    scopus 로고
    • Effects of cystic fibrosis lung disease on gas mixing indices derived from alveolar slope analysis
    • Horsley AR, Macleod KA, Robson AG, et al. Effects of cystic fibrosis lung disease on gas mixing indices derived from alveolar slope analysis. Respir Physiol Neurobiol 2008;162:197-203.
    • (2008) Respir Physiol Neurobiol , vol.162 , pp. 197-203
    • Horsley, A.R.1    Macleod, K.A.2    Robson, A.G.3
  • 8
    • 84938501003 scopus 로고    scopus 로고
    • A quantitative structural lung disease computed tomography outcome in young children with cystic fibrosis
    • Rosenow T, Oudraad MC, Murray CP, et al., Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST CF). PRAGMA-CF. A quantitative structural lung disease computed tomography outcome in young children with cystic fibrosis. Am J Respir Crit Care Med 2015;191:1158-65.
    • (2015) Am J Respir Crit Care Med , vol.191 , pp. 1158-1165
    • Rosenow, T.1    Oudraad, M.C.2    Murray, C.P.3
  • 9
    • 84885071273 scopus 로고    scopus 로고
    • Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D-CFTR mutation and preserved spirometry: A randomised controlled trial
    • Davies J, Sheridan H, Bell N, et al. Assessment of clinical response to ivacaftor with lung clearance index in cystic fibrosis patients with a G551D-CFTR mutation and preserved spirometry: a randomised controlled trial. Lancet Respir Med 2013;1:630-8.
    • (2013) Lancet Respir Med , vol.1 , pp. 630-638
    • Davies, J.1    Sheridan, H.2    Bell, N.3
  • 10
    • 84937735823 scopus 로고    scopus 로고
    • Feasibility of human lung ventilation imaging using highly polarized naturally abundant xenon and optimized three-dimensional steady-state free precession
    • Stewart NJ, Norquay G, Griffiths PD, et al. Feasibility of human lung ventilation imaging using highly polarized naturally abundant xenon and optimized three-dimensional steady-state free precession. Magn Reson Med 2015;74:346-52.
    • (2015) Magn Reson Med , vol.74 , pp. 346-352
    • Stewart, N.J.1    Norquay, G.2    Griffiths, P.D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.