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Journal Abstract Search

174 related items for PubMed ID: 23677424

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  • 23. Aortopulmonary collateral flow is related to pulmonary artery size and affects ventricular dimensions in patients after the fontan procedure.
    Latus H, Gummel K, Diederichs T, Bauer A, Rupp S, Kerst G, Jux C, Akintuerk H, Schranz D, Apitz C.
    PLoS One; 2013; 8(11):e81684. PubMed ID: 24303064
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  • 24. End-expiratory lung volume during arm and leg exercise in normal subjects and patients with cystic fibrosis.
    Alison JA, Regnis JA, Donnelly PM, Adams RD, Sullivan CE, Bye PT.
    Am J Respir Crit Care Med; 1998 Nov; 158(5 Pt 1):1450-8. PubMed ID: 9817692
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  • 25. The relationship between sleep disturbance and pulmonary function in stable pediatric cystic fibrosis patients.
    Amin R, Bean J, Burklow K, Jeffries J.
    Chest; 2005 Sep; 128(3):1357-63. PubMed ID: 16162729
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  • 29. Evaluation of ventilation maldistribution as an early indicator of lung disease in children with cystic fibrosis.
    Gustafsson PM, Aurora P, Lindblad A.
    Eur Respir J; 2003 Dec; 22(6):972-9. PubMed ID: 14680088
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  • 36. Aortopulmonary collaterals in single-ventricle congenital heart disease: how much do they count?
    Powell AJ.
    Circ Cardiovasc Imaging; 2009 May; 2(3):171-3. PubMed ID: 19808589
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  • 40. Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis.
    Gustafsson PM, De Jong PA, Tiddens HA, Lindblad A.
    Thorax; 2008 Feb; 63(2):129-34. PubMed ID: 17675316
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