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Human Pathology
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July 1, 1976
Aspartylglucosaminuria: unique biochemical and ultrastructural characteristics
J N Isenberg, H L Sharp
Hepato-Gastroenterology
|
June 1, 1986
Erythrocyte lipid alterations in pediatric cholestatic liver disease: relationship to serum bile acids
H 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 assay
H A Cynamon, J N Isenberg
Hepatology (Baltimore, Md.)
|
November 1, 1988
Evoked potential abnormalities in children with chronic cholestasis
H A Cynamon, K Norcross, J N Isenberg
Digestive Diseases and Sciences
|
October 1, 1987
Carbohydrate malabsorption is minimal in school-age cystic fibrosis children
R 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 fibrosis
J N Isenberg, P Y Hendrix, K L Cox
Journal of Pediatric Gastroenterology and Nutrition
|
January 1, 1982
Gastric acid hypersecretion in cystic fibrosis
K 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 determination
H A Cynamon, J N Isenberg, C H Nguyen
The Journal of Pediatrics
|
November 1, 1975
Letter: Leukocyte function in aspartylglucosaminuria
T 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 status
H A Cynamon, J N Isenberg, C H Nguyen
Page
of 5
Search research articles
Search
Showing results (11-20 of 41) with videos related to
Sort By:
Page
of 5
Human Pathology
|
July 1, 1976
Aspartylglucosaminuria: unique biochemical and ultrastructural characteristics
J N Isenberg, H L Sharp
Hepato-Gastroenterology
|
June 1, 1986
Erythrocyte lipid alterations in pediatric cholestatic liver disease: relationship to serum bile acids
H 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 assay
H A Cynamon, J N Isenberg
Hepatology (Baltimore, Md.)
|
November 1, 1988
Evoked potential abnormalities in children with chronic cholestasis
H A Cynamon, K Norcross, J N Isenberg
Digestive Diseases and Sciences
|
October 1, 1987
Carbohydrate malabsorption is minimal in school-age cystic fibrosis children
R 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 fibrosis
J N Isenberg, P Y Hendrix, K L Cox
Journal of Pediatric Gastroenterology and Nutrition
|
January 1, 1982
Gastric acid hypersecretion in cystic fibrosis
K 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 determination
H A Cynamon, J N Isenberg, C H Nguyen
The Journal of Pediatrics
|
November 1, 1975
Letter: Leukocyte function in aspartylglucosaminuria
T 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 status
H A Cynamon, J N Isenberg, C H Nguyen
Page
of 5