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Bibliografia
Fibrosi cistica: il ruolo della riabilitazione respiratoria nel trattamento del bambino
pubblicato nel Marzo - Aprile 2009 ne Il Fisioterapista - fascicolo n.2

Bibliografia

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  3. Connett GJ, Yeatman SL. Delayed diagnosis in cystic fibrosis patients homozygous for the Delta F508 mutation results in increased treatment to maintain health in childhood. Pediatr Pulmonol 2002; Suppl 24: A407.

  4. Goss CH. Airway clearance in cystic fibrosis. Respir Care 2003; 48: 20-1.

  5. O’Riordan TG. Inhaled antimicrobial therapy: from cystic fibrosis to flu. Respir Care 2000; 45: 836-45.

  6. Borsje P, de Jongste JC, Mouton JW, Tiddens HA. Aerosol therapy in cystic fibrosis: a survey of 54 centres. Pediatr Pulmonol 2000; 30: 368-76.

  7. Van der Schans C, Prasad A, Main E. Chest physiotherapy compared to no physiotherapy for cystic fibrosis. Cochrane Database Syst Rev 2000; 2: CD001401.

  8. Elkin SL, Fairney A, Burnett S et al. Vertebral deformities and low bone mineral density in adults with cystic fibrosis: a cross-sectional study. Osteoporos Int 2001; 12: 366-72.

  9. Nixon PA, Orenstein DM, Kelsey SF. Habitual physical activity in children and adolescents with cystic fibrosis. Med Sci Sports Exerc 2001; 33: 30-5.

  10. Andreasson B, Jonsson B, Kornfalt R, Nordmark E, Sandstrom S. Long-term effects of physical exercise on working capacity and pulmonary function in cystic fibrosis. Acta Pediatr Scand 1987; 76: 70-5.

  11. Hebestreit A, Kersting U, Basler B, Jeschke R, Hebestreit H. Exercise inhibits epithelial sodium channels in patients with cystic fibrosis. Am J Respir Crit Care Med 2001; 164: 443-6.

  12. Flower KA, Eden RI, Lomax L, Mann NM, Burgess J. New mechanical aid to physiotherapy in cystic fibrosis. Br Med J 1979; II: 630-1.

  13. Wood RE, Wanner A, Hirsch J, Farrell PM. Tracheal mucociliary transport in patients with cystic fibrosis and its stimulation by terbutaline. Am Rev Respir Dis 1975; 111: 733-8.

  14. Wong JW, Keens TG, Wannemaker EM, Douglas PT, Crozier N, Levison H. Effects of gravity on tracheal mucus transport rates in normal subjects and in patients with cystic fibrosis. Pediatrics 1977; 60: 146-52.

  15. Prasad SA, Main E. Finding evidence to support airway clearance techniques in cystic fibrosis. Disabil Rehabil 1998; 20: 235-46.

  16. Pryor JA, Webber BA. Physiotherapy techniques. In: Pryor JA, Prasad SA, eds Physiotherapy for Respiratory and Cardiac Problems, 3rd edn. Edinburgh: Churchill-Livingstone, 2002: 161-242.

  17. CF Family Education Program. Managing lung problems in cystic fibrosis. Baylor College of Medicine, Texas Children’s Hospital, Houston, Texas, 1994 (copies from Genentech, stock number LE0059).

  18. 18. McIlwaine PM, Wong LT, Peacock D, Davidson AG. Long-termcomparative trial of conventional postural drainage and percussion versus positive expiratory pressure physiotherapy in the treatment of cystic fibrosis. J Pediatr 1997; 131: 570-4.