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C L Morin

Showing results (61-70 of 76) with videos related to

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Digestive Diseases and Sciences|September 1, 1986
Effect of dietary fat and residues on fecal loss of sterols and on their microbial degradation in cystic fibrosisC Leroy, G Lepage, C L Morin, et al.
The American Journal of Clinical Nutrition|December 1, 1979
The fecal microflora and bile acids in children with cystic fibrosisC C Roy, G Delage, A Fontaine, et al.
The Journal of Pediatrics|January 1, 1986
Secretory diarrhea with protein-losing enteropathy, enterocolitis cystica superficialis, intestinal lymphangiectasia, and congenital hepatic fibrosis: a new syndromeV A Pelletier, N Galéano, P Brochu, et al.
Gastroenterology|May 1, 1981
Ménétrier's disease in children: report of a patient and review of sixteen other casesJ P Chouraqui, C C Roy, P Brochu, et al.
Pediatric Research|December 1, 1980
Gastric emptying and lingual lipase activity in cystic fibrosisM Roulet, A M Weber, Y Paradis, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1982
Hepatobiliary disease in cystic fibrosis: a survey of current issues and conceptsC C Roy, A M Weber, C L Morin, et al.
The New England Journal of Medicine|December 15, 1977
Abnormal biliary lipid composition in cystic fibrosis. Effect of pancreatic enzymesC C Roy, A M Weber, C L Morin, et al.
Gut|April 1, 1976
Relationship between bile acid malabsorption and pancreatic insufficiency in cystic fibrosisA M Weber, C C Roy, L Chartrand, et al.
Gastroenterology|October 1, 1981
Severe familial cholestasis in North American Indian children: a clinical model of microfilament dysfunction?A M Weber, B Tuchweber, I Yousef, et al.
Pediatrics|December 1, 1987
Primary sclerosing cholangitis in children: study of five cases and review of the literatureA Sisto, P Feldman, L Garel, et al.
Pageof 8

Showing results (61-70 of 76) with videos related to

Sort By:
Pageof 8
Digestive Diseases and Sciences|September 1, 1986
Effect of dietary fat and residues on fecal loss of sterols and on their microbial degradation in cystic fibrosisC Leroy, G Lepage, C L Morin, et al.
The American Journal of Clinical Nutrition|December 1, 1979
The fecal microflora and bile acids in children with cystic fibrosisC C Roy, G Delage, A Fontaine, et al.
The Journal of Pediatrics|January 1, 1986
Secretory diarrhea with protein-losing enteropathy, enterocolitis cystica superficialis, intestinal lymphangiectasia, and congenital hepatic fibrosis: a new syndromeV A Pelletier, N Galéano, P Brochu, et al.
Gastroenterology|May 1, 1981
Ménétrier's disease in children: report of a patient and review of sixteen other casesJ P Chouraqui, C C Roy, P Brochu, et al.
Pediatric Research|December 1, 1980
Gastric emptying and lingual lipase activity in cystic fibrosisM Roulet, A M Weber, Y Paradis, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1982
Hepatobiliary disease in cystic fibrosis: a survey of current issues and conceptsC C Roy, A M Weber, C L Morin, et al.
The New England Journal of Medicine|December 15, 1977
Abnormal biliary lipid composition in cystic fibrosis. Effect of pancreatic enzymesC C Roy, A M Weber, C L Morin, et al.
Gut|April 1, 1976
Relationship between bile acid malabsorption and pancreatic insufficiency in cystic fibrosisA M Weber, C C Roy, L Chartrand, et al.
Gastroenterology|October 1, 1981
Severe familial cholestasis in North American Indian children: a clinical model of microfilament dysfunction?A M Weber, B Tuchweber, I Yousef, et al.
Pediatrics|December 1, 1987
Primary sclerosing cholangitis in children: study of five cases and review of the literatureA Sisto, P Feldman, L Garel, et al.
Pageof 8