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N Isenberg

Showing results (11-20 of 41) with videos related to

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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
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1982
Gastric acid hypersecretion in cystic fibrosisK L Cox, J N Isenberg, M E Ament
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 15, 1984
A rapid method for erythrocyte membrane phospholipid determinationH A Cynamon, J N Isenberg, C H Nguyen
The Journal of Pediatrics|November 1, 1975
Letter: Leukocyte function in aspartylglucosaminuriaT A Fleisher, J N Isenberg, H L Sharp
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 30, 1985
Erythrocyte malondialdehyde release in vitro: a functional measure of vitamin E statusH A Cynamon, J N Isenberg, C H Nguyen
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
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
Journal of Pediatric Gastroenterology and Nutrition|January 1, 1982
Gastric acid hypersecretion in cystic fibrosisK L Cox, J N Isenberg, M E Ament
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 15, 1984
A rapid method for erythrocyte membrane phospholipid determinationH A Cynamon, J N Isenberg, C H Nguyen
The Journal of Pediatrics|November 1, 1975
Letter: Leukocyte function in aspartylglucosaminuriaT A Fleisher, J N Isenberg, H L Sharp
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 30, 1985
Erythrocyte malondialdehyde release in vitro: a functional measure of vitamin E statusH A Cynamon, J N Isenberg, C H Nguyen
Pageof 5