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N Isenberg

Showing results (1-10 of 28) with videos related to

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Advances in Pediatrics|January 1, 1977
The infant and hepatitis B virus infectionJ N Isenberg
Journal of Pediatric Surgery|August 1, 1984
Stimulation of bile output by gastrointestinal hormones following portoenterostomy for biliary atresiaJ N Isenberg, M Z Schwartz
European Journal of Pediatrics|September 1, 1987
Application of a new test for vitamin E deficiency to cystic fibrosisH A Cynamon, J N Isenberg
The Journal of Pediatrics|May 1, 1975
Aspartylglucosaminuria: psychomotor retardation masquerading as a mucopolysaccharidosisJ N Isenberg, H L Sharp
Human Pathology|July 1, 1976
Aspartylglucosaminuria: unique biochemical and ultrastructural characteristicsJ N Isenberg, H L Sharp
Hepato-Gastroenterology|June 1, 1986
Erythrocyte lipid alterations in pediatric cholestatic liver disease: relationship to serum bile acidsH A Cynamon, J N Isenberg
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1987
Characterization of vitamin E status in cholestatic children by conventional laboratory standards and a new functional assayH A Cynamon, J N Isenberg
Hepatology (Baltimore, Md.)|November 1, 1988
Evoked potential abnormalities in children with chronic cholestasisH A Cynamon, K Norcross, J N Isenberg
Digestive Diseases and Sciences|October 1, 1987
Carbohydrate malabsorption is minimal in school-age cystic fibrosis childrenR D Hoffman, J N Isenberg, G K Powell
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1983
Effect of short-term cimetidine administration on fecal bile acid losses in cystic fibrosisJ N Isenberg, P Y Hendrix, K L Cox
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Advances in Pediatrics|January 1, 1977
The infant and hepatitis B virus infectionJ N Isenberg
Journal of Pediatric Surgery|August 1, 1984
Stimulation of bile output by gastrointestinal hormones following portoenterostomy for biliary atresiaJ N Isenberg, M Z Schwartz
European Journal of Pediatrics|September 1, 1987
Application of a new test for vitamin E deficiency to cystic fibrosisH A Cynamon, J N Isenberg
The Journal of Pediatrics|May 1, 1975
Aspartylglucosaminuria: psychomotor retardation masquerading as a mucopolysaccharidosisJ N Isenberg, H L Sharp
Human Pathology|July 1, 1976
Aspartylglucosaminuria: unique biochemical and ultrastructural characteristicsJ N Isenberg, H L Sharp
Hepato-Gastroenterology|June 1, 1986
Erythrocyte lipid alterations in pediatric cholestatic liver disease: relationship to serum bile acidsH A Cynamon, J N Isenberg
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1987
Characterization of vitamin E status in cholestatic children by conventional laboratory standards and a new functional assayH A Cynamon, J N Isenberg
Hepatology (Baltimore, Md.)|November 1, 1988
Evoked potential abnormalities in children with chronic cholestasisH A Cynamon, K Norcross, J N Isenberg
Digestive Diseases and Sciences|October 1, 1987
Carbohydrate malabsorption is minimal in school-age cystic fibrosis childrenR D Hoffman, J N Isenberg, G K Powell
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1983
Effect of short-term cimetidine administration on fecal bile acid losses in cystic fibrosisJ N Isenberg, P Y Hendrix, K L Cox
Pageof 3