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Journal Abstract Search

194 related items for PubMed ID: 24847094

  • 41. Effects of noninvasive ventilation on treadmill 6-min walk distance and regional chest wall volumes in cystic fibrosis: randomized controlled trial.
    Lima CA, Andrade Ade F, Campos SL, Brandão DC, Fregonezi G, Mourato IP, Aliverti A, Britto MC.
    Respir Med; 2014 Oct; 108(10):1460-8. PubMed ID: 25195137
    [Abstract] [Full Text] [Related]

  • 42. Comparison of Flutter device and chest physical therapy in the treatment of cystic fibrosis pulmonary exacerbation.
    Gondor M, Nixon PA, Mutich R, Rebovich P, Orenstein DM.
    Pediatr Pulmonol; 1999 Oct; 28(4):255-60. PubMed ID: 10497374
    [Abstract] [Full Text] [Related]

  • 43. Small airway deposition of dornase alfa during exacerbations in cystic fibrosis; a randomized controlled clinical trial.
    Bakker EM, Volpi S, Salonini E, Müllinger B, Kroneberg P, Bakker M, Hop WC, Assael BM, Tiddens HA.
    Pediatr Pulmonol; 2014 Feb; 49(2):154-61. PubMed ID: 23913868
    [Abstract] [Full Text] [Related]

  • 44. What is the best airway clearance technique in cystic fibrosis?
    Main E.
    Paediatr Respir Rev; 2013 May; 14 Suppl 1():10-2. PubMed ID: 23541002
    [Abstract] [Full Text] [Related]

  • 45. Physiotherapy in cystic fibrosis: optimising techniques to improve outcomes.
    Rand S, Hill L, Prasad SA.
    Paediatr Respir Rev; 2013 Dec; 14(4):263-9. PubMed ID: 24209461
    [Abstract] [Full Text] [Related]

  • 46. Lung function in the aging Swedish cystic fibrosis population.
    Dennersten U, Lannefors L, Höglund P, Hellberg K, Johansson H, Lagerkvist AL, Ortfelt M, Sahlberg M, Eriksson L.
    Respir Med; 2009 Jul; 103(7):1076-82. PubMed ID: 19233629
    [Abstract] [Full Text] [Related]

  • 47. Lung clearance index predicts pulmonary exacerbations in young patients with cystic fibrosis.
    Vermeulen F, Proesmans M, Boon M, Havermans T, De Boeck K.
    Thorax; 2014 Jan; 69(1):39-45. PubMed ID: 24021874
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  • 51. The immediate effect of physiotherapy and aerosol treatment on pulmonary function in children with cystic fibrosis.
    Kerrebijn KF, Veentjer R, Bonzet-vd Water E.
    Eur J Respir Dis; 1982 Jan; 63(1):35-42. PubMed ID: 7067754
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  • 52. Airway responsiveness to hyperosmolar saline challenge in cystic fibrosis: a pilot study.
    Rodwell LT, Anderson SD.
    Pediatr Pulmonol; 1996 May; 21(5):282-9. PubMed ID: 8726153
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  • 54. Multiple breath inert gas washout as a measure of ventilation distribution in children with cystic fibrosis.
    Aurora P, Gustafsson P, Bush A, Lindblad A, Oliver C, Wallis CE, Stocks J.
    Thorax; 2004 Dec; 59(12):1068-73. PubMed ID: 15563707
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  • 55. Effects of a short-term rehabilitation program on airway inflammation in children with cystic fibrosis.
    Moeller A, Stämpfli SF, Rueckert B, Rechsteiner T, Hamacher J, Wildhaber JH.
    Pediatr Pulmonol; 2010 Jun; 45(6):541-51. PubMed ID: 20503278
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  • 56. The impact of re-education of airway clearance techniques (REACT) on adherence and pulmonary function in patients with cystic fibrosis.
    Zanni RL, Sembrano EU, Du DT, Marra B, Bantang R.
    BMJ Qual Saf; 2014 Apr; 23 Suppl 1():i50-5. PubMed ID: 24608551
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  • 57. Effect of supervised training on FEV1 in cystic fibrosis: a randomised controlled trial.
    Kriemler S, Kieser S, Junge S, Ballmann M, Hebestreit A, Schindler C, Stüssi C, Hebestreit H.
    J Cyst Fibros; 2013 Dec; 12(6):714-20. PubMed ID: 23588193
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  • 59. Long-term multicentre randomised controlled study of high frequency chest wall oscillation versus positive expiratory pressure mask in cystic fibrosis.
    McIlwaine MP, Alarie N, Davidson GF, Lands LC, Ratjen F, Milner R, Owen B, Agnew JL.
    Thorax; 2013 Aug; 68(8):746-51. PubMed ID: 23407019
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