Raised serum soluble interleukin-2 receptor concentrations in cystic fibrosis patients with and without evidence of lung disease.

Author:

Dagli E,Warner J A,Besley C R,Warner J O

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference21 articles.

1. Cystic fibrosis: a review of pulmonary infections and interventions;Thomassen, M.J.; Demko, C.A.; Doershuk, C.F.;Pediatr Pulmonol,1987

2. Granulocyte neutral proteases and pseudomonas elastase as possible causes of airway damage in patients with cystic fibrosis. J7 Infect Dts;Suter, S.; Schaad, U.B.; Roux, L.; Nydegger, U.E.; Waldvogel, F.A.,1984

3. Immune complex mediated tissue damage in the lungs of cystic fibrosis patients with chronic Pseudomonas aeruginosa infection;Hoiby, N.; Schiotz, P.O.;Acta Paediatr Scand,1982

4. Alternate-day prednisone reduces morbidity and improves function in cystic fibrosis;Auerbach, H.S.; Williams, M.; Kirkpatrick, J.A.; Colten, H.R.;Lancet,1985

5. Immunologic aspects of cystic fibrosis;Doring, G.; Albus, A.; Hoiby, N.;Chest,1988

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