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References
Fisioterapia e riabilitazione in fibrosi cistica
published in May - June 2006 - in Il Fisioterapista - issue n.3

There are no translations available.

Bibliografia

  1. Godfey S, Mearns M. Pulmonary function and response to exercise in cystic fibrosis. Arch Dis Child 1971; 46: 144-51.

  2. Coates AL, Boyce P, Muller D et al. The role of nutritional status, airway obstruction, hypoxia, and abnormalities in serum lipid composition in limiting exercise tolerance in children with cystic fibrosis. Acta Paediatr Scand 1980; 69: 353-8.

  3. Marcotte JE, Grisdale RK, Levison H et al. Multiple factors limit exercise capacity in cystic fibrosis. Pediatr Pulmonol 1986; 2: 274-81.

  4. Marcotte JE, Canny GJ, Grisdale R et al. Effects of nutritional status on exercise performance in advanced cystic fibrosis. Chest 1986; 90: 375-9.

  5. Corbetta C, Seia M, Bassotti A et al. Screening for cystic fibrosis in newborn infants: results of a pilot programme based on a two tier protocol (IRT/DNA/IRT) in the Italian population. J Med Screen 2002; 9: 60-3.

  6. Castellani C, Bonizzato A, Cabrini G et al. Newborn screening strategy for cystic fibrosis: a field study in an area with high allelic heterogeneity. Acta Paediatr 1977; 86: 497-502.

  7. Castellani C. Dieci anni dalla scoperta del gene della fibrosi cistica: implicazioni cliniche. Aggiornamenti di fisiopatologia e terapia in pediatria 2000; 10: 14-21.

  8. Frederiksen B, Lanng S, Kock C et al. Improved survival in the Danish center-treated cystic fibrosis patients: results of aggressive treatment. Pediatr Pulmonol 1996; 21: 153-8.

  9. Anguiano A, Oates RD, Amos JA et al. Congenital absence of the vas deferens. A primarily genital form of cystic fibrosis. JAMA 1992; 267: 1704-7.

  10. Cohn JA, Friedman KJ, Noone PG et al. Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis. N Engl J Med 1998; 339: 635-8.

  11. Alton EWFW, Currie D, Logan-Sinclair R et al. Nasal potential difference: a clinical diagnostic test for cystic fibrosis. Eur Respir J 1990; 3: 922-6.

  12. Rosenstein BJ, Cutting GR. The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation consensus panel. J Paediatr 1998; 132: 589-95.


 
There are no translations available.