Mukoviszidose

  • Thomas O. F. Wagner

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Literatur

  1. Crispin AR, Norman AP (1984) The systematic evaluation of the chest radio-graph in cystic fibrosis. Pediatr Radiol 2: 101–106Google Scholar
  2. Cystic fibrosis Conference Reports (1978) CF patient evaluations and scoring systems. Tucson, AZ 2(2)Google Scholar
  3. Egan ME, Pearson M, Weiner SA et al. (2004) Curcumin, a major constituent of turmeric, corrects cystic fibrosis defects. Science 304: 600–602CrossRefPubMedGoogle Scholar
  4. Gibson LE, Cooke RE (1959) A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis. Pediatrics 23:545–549PubMedGoogle Scholar
  5. Hoiby N (1993) Antibiotic therapy for chronic infection of Pseudomonas in the lung. Annu Rev Med 44:1–10CrossRefPubMedGoogle Scholar
  6. Kraemer R, Rüdeberg A, Kläy M, Rossi E (1979) Relationship between clinical conditions, radiographic findings and pulmonary functions in patients with cystic fibrosis. Helv Paediat Acta 34: 417–428PubMedGoogle Scholar
  7. Riordan JR, Rommens JM, Kerem B et al. (1989) Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science 245: 1066–1073PubMedGoogle Scholar
  8. Shwachman H, Kulczycki LL (1958) A report of one hundred and one patients with cystic fibrosis of the pancreas studied over a five to fourteen year period. Am J Dis Child 96: 6–15Google Scholar
  9. Steinkamp G (1991) Antibiotikainhalation bei zystischer Fibrose. Monatschr Kinderheilkd 139: 73–80Google Scholar
  10. Stern RC (1997) The diagnosis of cystic fibrosis. New Engl J Med 336(7): 487–491CrossRefPubMedGoogle Scholar
  11. Stern M, Wiedemann B (2003) Qualitätssicherung Mukoviszidose — Überblick über den Gesundheitszustand der Patienten 2002. Wissenschaftlicher Beirat Qualitätssicherung Mukoviszidose, HannoverGoogle Scholar
  12. Szaff M, Hoiby N, Flensborg EW (1983) Frequent antibiotic therapy improves survival of cystic fibrosis patients with chronic pseudomonas aeruginosa infection. Acta Paediatr Scand 72: 651PubMedGoogle Scholar
  13. Wood RE, Boat TF, Doershuk CF (1976) State of the art: cystic fibrosis. Am Rev Respir Dis 113: 833PubMedGoogle Scholar
  14. Wilschanski M, Yahav Y, Yaacov Y, Blau H, Bentur L, Rivlin J et al. (2003) Gentamicin-induced correction of CFTR function in patients with cystic fibrosis and CFTR stop mutations. N Engl J Med 349: 1433–1441CrossRefPubMedGoogle Scholar
  15. Yankaskas JR, Marshall BC, Sufian B, Simon RH, Rodman D (2004) Cystic fibrosis adult care: Consensus Conference Report. Chest 125: 1S–39CrossRefPubMedGoogle Scholar

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© Springer-Verlag Heidelberg 2005

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  • Thomas O. F. Wagner

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