CFTR gene mutations and the pancreatic phenotype

Pediatric Pulmonology

Volumn 28, Issue SUPPL. 19, 1999, Pages 127-128

  Durie, P R ^a   Ahmed, N ^a   Corey, M ^a   Zielenski, J ^a   Ellis, L ^a   Tullis, E ^a   Tsui, L C ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0004330627     PISSN: 87556863     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (7)

1. Gaskin K, Gurwitz D, Dune PR, Levison H, Forstner G. Improved respiratory prognosis in patients with cystic fibrosis with normal fat malabsorption. J Pediatr 1982; 100:857-862.
2. Kristidis P, Bozon D, Corey M, Markiewicz D, Rommens J, Tsui L-C, Durie P. Genetic determination of exocrine pancreatic function in cystic fibrosis. Am J Hum Genet 1992; 50:1178-1184.
3. Zielenski J, Tsui L-C. Cystic fibrosis: genotypic and phenotypic variations. Ann Rev Gen 1995; 29:777-807.
4. Wilschanski M, Zielenski J, Markiewicz D, Tsui L-C, Corey M, Levison H, Durie P. Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations. J Pediatr 1995; 127:705-710.
5. Gaskin KJ, Durie PR, Lee L, Hill R, Forstner GG. Colipase and lipase secretion in childhood-onset pancreatic insufficiency: delineation of patients with steatorrhea secondary to relative colipase deficiency. Gastroenterology 1984; 86:1-7.
6. Kopelman H, Durie P, Gaskin K, Weizman Z, Forstner G. Pancreatic fluid secretion and protein hyperconcentration in cystic fibrosis. N Engl J Med. 1985;312;329-34.
7. Kopelman H, Corey M, Gaskin K, Durie P, Weizman Z, Forstner G. Impaired chloride secretion as well as bicarbonate secretion underlies the fluid secretory defect in the cystic fibrosis pancreas. Gastroenterology 1988; 95:349-355. Supported by NIH and the Canadian Cystic Fibrosis Foundation