Publikationen

Publikationen

Broschüren und Publikationen zum Thema Sport und Mukoviszidose finden Sie auf dieser Seite.



Literatur

  • Bradley, J., O'Neill, B., Kent, L., Hulzebos, E. H., Arets, B, Hebestreit, H. (2015). Physical activity assessment in cystic fibrosis: A position statement. Journal of Cystic Fibrosis, 14 (6), e25-e32.
  • Meer, K. de, Gulmans, V. A., Laag, J. van der (1999). Peripheral muscle weakness and exercise capacity in children with cystic fibrosis. American journal of respiratory and critical care medicine, 159 (3), 748-754.
  • Gruber, W., Orenstein, D. M., Braumann, K. M., Paul, K., Hüls, G. (2011). Effects of an exercise program in children with cystic fibrosis: are there differences between females and males? The Journal of pediatrics, 158 (1), 71-76.
  • Hebestreit, H., Arets, H. G., Aurora, P., Boas, S., Cerny, F., Hulzebos, E. H. et al. (2015). Statement on exercise testing in cystic fibrosis. Respiration, 90 (4), 332-351.
  • Hebestreit, A., Kersting, U., Basler, B., Jeschke, R., Hebestreit, H. (2001). Exercise inhibits epithelial sodium channels in patients with cystic fibrosis. American Journal of respiratory and critical care medicine, 164 (3), 443-6.
  • Hebestreit, H., Hulzebos, E. H., Schneiderman, J. E., Karila, C., Boas, S. R., Kriemler, S., Dwyer, T., Sahlberg, M., Urquhart, D. S., Lands, L. C., Ratjen, F., Takken, T., Varanistkaya, L., Rücker, V., Hebestreit, A., Usemann, J., Radtke, T. (2018). Prognostic value of CPET in CF study group. Cardiopulmonary exercise testing provides additional prognostic information in cystic fibrosis. American Journal of respiratory and critical care medicine, 15, Epub ahead of print.
  • Javadpour, S. M., Selvadurai, H., Wilkes, D. L., Schneiderman-Walker, J., Coates, A. L. (2005). Does carbon dioxide retention during exercise predict a more rapid decline in FEV1 in cystic fibrosis? Archives of disease in childhood, 90 (8), 792-795.
  • Klijn, P. H., Terheggen‐Lagro, S. W., Ent ,C. K. van der, Net, J. van der, Kimpen, J. L., Helders, P. J. (2003). Anaerobic exercise in pediatric cystic fibrosis. Pediatric pulmonology, 36 (3), 223-229.
  • Kriemler, S., Kieser, S., Junge, S., Ballmann, M., Hebestreit, A., Schindler, C., Stüssi, C., Hebestreit, H. (2013). Effect of supervised training on FEV1 in cystic fibrosis: A randomised controlled trial. Journal of Cystic Fibrosis, 12, 714-720.
  • Moorcroft, A. J., Dodd, M. E., Webb, A. K. (1997). Exercise testing and prognosis in adult cystic fibrosis. Thorax, 52 (3), 291-293.
  • Nixon, P. A., Orenstein, D. M., Kelsey, S. F., Doershuk, C. F. (1992). The prognostic value of exercise testing in patients with cystic fibrosis. The New England Journal, 327, 1785-1788.
  • Pianosi, P., LeBlanc, J., Almudevar, A. (2005). Relationship between FEV1 and peak oxygen uptake in children with cystic fibrosis. Pediatric pulmonology, 40 ( 4), 324-329.
  • Pianosi, P., LeBlanc, J., Almudevar, A. (2005). Peak oxygen uptake and mortality in children with cystic fibrosis. Thorax, 60 (1), 50-54.
  • Radtke, T., Nolan, S. J., Hebestreit, H., Kriemler, S. (2015). Physical exercise training for cystic fibrosis. Cochrane database of systematic reviews, 28 (6), CD002768.
  • Radtke, T., Nevitt, S. J., Hebestreit, H., Kriemler, S. (2017). Physical exercise training for cystic fibrosis. Cochrane database of systematic reviews, 11, CD002768.
  • Radtke, T., Hebestreit, H., Gallati, S., Schneiderman, J. E., Braun, J., Stevens, D., Hulzebos, E. H., Takken, T., Boas, S. R., Urquhart, D. S., Lands, L. C., Tejero, S., Sovtic, A., Dwyer, T., Petrovic, M., Harris, R. A., Karila, C., Savi, D., Usemann, J., Mei-Zahav, M., Hatziagorou, E., Ratjen, F., Kriemler, S.; CFTR-Exercise study group (2018). CFTR Genotype and Maximal Exercise Capacity in Cystic Fibrosis: A Cross-sectional Study. Annals of the American Thoracic Society, 15, 209-216.
  • Schneiderman-Walker, J., Wilkes, D.L., Strug, L., Lands, L. C., Pollock, S. L., Selvadurai, H. C., et al. (2005). Sex differences in habitual physical activity and lung function decline in children with cystic fibrosis. The Journal of pediatrics, 147 (3), 321-326.
  • Schneiderman, J. E., Wilkes, D. L., Atenafu, E. G., Nguyen, T., Wells, G. D., Alarie, N., Tullis, E., Lands, L. C., Coates, A. L., Corey, M., Ratjen, F. (2014). Longitudinal relationship between physical activity and lung health in patients with cystic fibrosis. European Respiratory Journal, 43 (3), 817-23.
  • Selvadurai, H. C., Allen, J., Sachinwalla, T., Macauley, J., Blimkie, C. J., Van Asperen, P. P. (2003). Muscle function and resting energy expenditure in female athletes with cystic fibrosis. American journal of respiratory and critical care medicine, 168 (12), 1476-1480.
  • Selvadurai, H. C., Blimkie, C. J., Cooper, P. J., Mellis, C. M., Asperen, P.P. van (2004). Gender differences in habitual activity in children with cystic fibrosis. Archives of disease in childhood, 89 (10), 928-933.
  • Swisher, A. K., Hebestreit, H., Mejia-Downs, A., Lowman, J. D., Gruber, W., Nippins, M., et al. (2015). Exercise and habitual physical activity for people with cystic fibrosis: expert consensus, evidence-based guide for advising patients. Cardiopulmonary Physical Therapy Journal, 26 (4), 85-98.
  • Williams, C. A., Benden, C., Stevens, D., Radtke, T. (2010). Exercise training in children and adolescents with cystic fibrosis: theory into practice. International journal of pediatrics, 2010: 670640. Doi: 10.1155/2010/670640.
Zuletzt aktualisiert: 17.01.2019