Cystic fibrosis. 6. Gastrointestinal and nutritional aspects.

Author:

Kopelman H

Publisher

BMJ

Subject

Pulmonary and Respiratory Medicine

Reference25 articles.

1. A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in;Corey, M.; McLaughlin, F.J.; Williams, M.; Levison, H.;Boston and Toronto. J Clin Epidemiol,1988

2. Pancreatic fluid and protein hyperconcentration in cystic fibrosis;Kopelman, H.; Durie, P.; Gaskin, K.; Weizman, Z.; Forstner, G.;N Engi J Med,1985

3. Colipase and lipase secretion in childhood onset of pancreatic insufficiency: delineation of patients with steatorrhea with relative colipase deficiency;Gaskin, K.; Durie, P.; Lee, L.; Hill, R.; Forstner, G.;Gastroenterology,1984

4. The use of a synthetic prostaglandin E, analogue as an adjunct to pancreatic enzyme replacement in cystic fibrosis;Cleghom, G.J.; Shepherd, R.W.; Holt, T.L.;Scand J Gastroenterol,1988

5. Gastric acid hypersecretion in cystic fibrosis;Cox, K.L.; Isenberg, J.N.; Ament, M.E.;J Ped Gastroenterol Nutr,1982

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