1. Serum alkaline phosphatase in cystic fibrosis-interpretation of elevated values based on electrophoretic isoenzyme analyses;F, Boat T.; F, Doershuk C.; C, Stern R.; W, Matthews L.;Clin Pediatr (Phila),1974
2. Symptomatic hepatic disease in cystic fibrosis: incidence, course, and outcome of portal changes. Furthermore, Feigelson et al.28 recently stressed that children with CF and clinically apparent liver involvement (16%) may have two different types of cirrhosis, one being of the cholestatic type systemic shunting;C, Stern R.; P, Stevens D.; F, Boat T.; F, Doershuk C.; Izant R J, Jr, Matthews L.W.;Gastroenterology,1976
3. Liver disease in cystic fibrosis;P, Mowat A.;Maandschr Kindergeneesk,1975
4. Hepatic changes in young infants with cystic fibrosis: possible relation to focal and the other with little or no cholestasis. In the present study we noted considerable variation in the character of the cellular infiltrate in the liver biopsies reviewed, ranging from a predominance of polybiliary cirrhosis;H, Oppenheimer E.; R, Esterly J.;JPediatr,1975
5. Immediate hypersensitivity in patients with cystic fibrosis;D, Allan J.; D, Moss A.; C, Wallwork J.; H, McFarlane;Clin Allergy,1975