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L J Elsas

Showing results (11-20 of 139) with videos related to

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Molecular Genetics and Metabolism|October 11, 2001
Structure-function analyses of a common mutation in blacks with transferase-deficiency galactosemiaK Lai, L J Elsas
Annual Review of Medicine|January 1, 1992
Glucose transportersL J Elsas, N Longo
Advances in Pediatrics|September 22, 1998
Human glucose transportersN Longo, L J Elsas
Biochemical Medicine|May 1, 1975
Subcellular distribution and cofactor function of human branched chain alpha-ketoacid dehydrogenase in normal and mutant cultured skin fibroblastsD J Danner, L J Elsas
Biochimica Et Biophysica Acta|March 17, 1972
Hexose transport and phosphorylation by hamster kidney cortex slices and averted jejunal ringsL J Elsas, R C Macdonell
Vitamins and Hormones|January 1, 1986
Genetic defects in vitamin utilization. Part I: General aspects and fat-solumbe vitaminsL J Elsas, D B McCormick
The Journal of Pediatrics|August 1, 1973
Familial glucose-galactose malabsorption: remission of glucose intoleranceL J Elsas, D W Lambe
Annals of the New York Academy of Sciences|January 1, 1982
The role of thiamin in maple syrup urine diseaseL J Elsas, D J Danner
The Journal of Pediatrics|April 1, 1975
Classic phenylketonuria: diagnosis through heterozygote detectionR F Griffin, L J Elsas
American Journal of Medical Genetics|January 1, 1980
Application of benefit-to-cost analysis to an X-linked recessive cardiac and humeroperoneal neuromuscular diseaseM L Wright, L J Elsas
Pageof 14

Showing results (11-20 of 139) with videos related to

Sort By:
Pageof 14
Molecular Genetics and Metabolism|October 11, 2001
Structure-function analyses of a common mutation in blacks with transferase-deficiency galactosemiaK Lai, L J Elsas
Annual Review of Medicine|January 1, 1992
Glucose transportersL J Elsas, N Longo
Advances in Pediatrics|September 22, 1998
Human glucose transportersN Longo, L J Elsas
Biochemical Medicine|May 1, 1975
Subcellular distribution and cofactor function of human branched chain alpha-ketoacid dehydrogenase in normal and mutant cultured skin fibroblastsD J Danner, L J Elsas
Biochimica Et Biophysica Acta|March 17, 1972
Hexose transport and phosphorylation by hamster kidney cortex slices and averted jejunal ringsL J Elsas, R C Macdonell
Vitamins and Hormones|January 1, 1986
Genetic defects in vitamin utilization. Part I: General aspects and fat-solumbe vitaminsL J Elsas, D B McCormick
The Journal of Pediatrics|August 1, 1973
Familial glucose-galactose malabsorption: remission of glucose intoleranceL J Elsas, D W Lambe
Annals of the New York Academy of Sciences|January 1, 1982
The role of thiamin in maple syrup urine diseaseL J Elsas, D J Danner
The Journal of Pediatrics|April 1, 1975
Classic phenylketonuria: diagnosis through heterozygote detectionR F Griffin, L J Elsas
American Journal of Medical Genetics|January 1, 1980
Application of benefit-to-cost analysis to an X-linked recessive cardiac and humeroperoneal neuromuscular diseaseM L Wright, L J Elsas
Pageof 14