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G Forstner

Showing results (111-120 of 130) with videos related to

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Gut|September 1, 1986
Bile acid secretion in cystic fibrosis: evidence for a defect unrelated to fat malabsorptionZ Weizman, P R Durie, H R Kopelman, et al.
Gastroenterology|December 1, 1996
Shwachman syndrome: exocrine pancreatic dysfunction and variable phenotypic expressionD R Mack, G G Forstner, M Wilschanski, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1984
Pancreatic function testing in cystic fibrosisP R Durie, K J Gaskin, M Corey, et al.
The Biochemical Journal|September 1, 1992
Tissue-specific expression of a rat intestinal mucin-like peptideG Xu, D Wang, L J Huan, et al.
Gastroenterology|July 1, 1982
Steatorrhea and pancreatic insufficiency in Shwachman syndromeR E Hill, P R Durie, K J Gaskin, et al.
The Journal of Clinical Investigation|February 1, 1982
Colipase and maximally activated pancreatic lipase in normal subjects and patients with steatorrheaK J Gaskin, P R Durie, R E Hill, et al.
Gastroenterology|September 1, 1985
Bentiromide test for assessing pancreatic dysfunction using analysis of para-aminobenzoic acid in plasma and urine. Studies in cystic fibrosis and Shwachman's syndromeZ Weizman, G G Forstner, K J Gaskin, et al.
Journal of Clinical Pathology|April 1, 1980
Immunoassay of serum conjugates of cholic acid in cystic fibrosisG P Davidson, M Corey, F Morad-Hassel, et al.
The New England Journal of Medicine|March 9, 1989
Microvillus inclusion disease: an inherited defect of brush-border assembly and differentiationE Cutz, J M Rhoads, B Drumm, et al.
Pediatric Research|August 1, 1992
Decline of exocrine pancreatic function in cystic fibrosis patients with pancreatic sufficiencyR T Couper, M Corey, D J Moore, et al.
Pageof 13

Showing results (111-120 of 130) with videos related to

Sort By:
Pageof 13
Gut|September 1, 1986
Bile acid secretion in cystic fibrosis: evidence for a defect unrelated to fat malabsorptionZ Weizman, P R Durie, H R Kopelman, et al.
Gastroenterology|December 1, 1996
Shwachman syndrome: exocrine pancreatic dysfunction and variable phenotypic expressionD R Mack, G G Forstner, M Wilschanski, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1984
Pancreatic function testing in cystic fibrosisP R Durie, K J Gaskin, M Corey, et al.
The Biochemical Journal|September 1, 1992
Tissue-specific expression of a rat intestinal mucin-like peptideG Xu, D Wang, L J Huan, et al.
Gastroenterology|July 1, 1982
Steatorrhea and pancreatic insufficiency in Shwachman syndromeR E Hill, P R Durie, K J Gaskin, et al.
The Journal of Clinical Investigation|February 1, 1982
Colipase and maximally activated pancreatic lipase in normal subjects and patients with steatorrheaK J Gaskin, P R Durie, R E Hill, et al.
Gastroenterology|September 1, 1985
Bentiromide test for assessing pancreatic dysfunction using analysis of para-aminobenzoic acid in plasma and urine. Studies in cystic fibrosis and Shwachman's syndromeZ Weizman, G G Forstner, K J Gaskin, et al.
Journal of Clinical Pathology|April 1, 1980
Immunoassay of serum conjugates of cholic acid in cystic fibrosisG P Davidson, M Corey, F Morad-Hassel, et al.
The New England Journal of Medicine|March 9, 1989
Microvillus inclusion disease: an inherited defect of brush-border assembly and differentiationE Cutz, J M Rhoads, B Drumm, et al.
Pediatric Research|August 1, 1992
Decline of exocrine pancreatic function in cystic fibrosis patients with pancreatic sufficiencyR T Couper, M Corey, D J Moore, et al.
Pageof 13