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G G Forstner

Showing results (51-60 of 72) with videos related to

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The Journal of Pediatrics|December 1, 1978
Iatrogenic hyperuricemia in children with cystic fibrosisG P Davidson, F M Hassel, D Crozier, et al.
The Biochemical Journal|September 1, 1979
The role of disulphide bonds in human intestinal mucinJ F Forstner, I Jabbal, R Qureshi, et al.
Pediatric Research|July 1, 1982
Evidence for a primary defect of pancreatic HCO3-secretion in cystic fibrosisK J Gaskin, P R Durie, M Corey, et al.
The Journal of Pediatrics|September 1, 1995
Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic-sufficient patients with cystic fibrosisR T Couper, M Corey, P R Durie, et al.
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.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
The Journal of Pediatrics|December 1, 1978
Iatrogenic hyperuricemia in children with cystic fibrosisG P Davidson, F M Hassel, D Crozier, et al.
The Biochemical Journal|September 1, 1979
The role of disulphide bonds in human intestinal mucinJ F Forstner, I Jabbal, R Qureshi, et al.
Pediatric Research|July 1, 1982
Evidence for a primary defect of pancreatic HCO3-secretion in cystic fibrosisK J Gaskin, P R Durie, M Corey, et al.
The Journal of Pediatrics|September 1, 1995
Longitudinal evaluation of serum trypsinogen measurement in pancreatic-insufficient and pancreatic-sufficient patients with cystic fibrosisR T Couper, M Corey, P R Durie, et al.
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.
Pageof 8