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Molecular Genetics and Metabolism
|
October 11, 2001
Structure-function analyses of a common mutation in blacks with transferase-deficiency galactosemia
K Lai, L J Elsas
Annual Review of Medicine
|
January 1, 1992
Glucose transporters
L J Elsas, N Longo
Advances in Pediatrics
|
September 22, 1998
Human glucose transporters
N 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 fibroblasts
D J Danner, L J Elsas
Biochimica Et Biophysica Acta
|
March 17, 1972
Hexose transport and phosphorylation by hamster kidney cortex slices and averted jejunal rings
L J Elsas, R C Macdonell
Vitamins and Hormones
|
January 1, 1986
Genetic defects in vitamin utilization. Part I: General aspects and fat-solumbe vitamins
L J Elsas, D B McCormick
The Journal of Pediatrics
|
August 1, 1973
Familial glucose-galactose malabsorption: remission of glucose intolerance
L J Elsas, D W Lambe
Annals of the New York Academy of Sciences
|
January 1, 1982
The role of thiamin in maple syrup urine disease
L J Elsas, D J Danner
The Journal of Pediatrics
|
April 1, 1975
Classic phenylketonuria: diagnosis through heterozygote detection
R 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 disease
M L Wright, L J Elsas
Page
of 14
Search research articles
Search
Showing results (11-20 of 139) with videos related to
Sort By:
Page
of 14
Molecular Genetics and Metabolism
|
October 11, 2001
Structure-function analyses of a common mutation in blacks with transferase-deficiency galactosemia
K Lai, L J Elsas
Annual Review of Medicine
|
January 1, 1992
Glucose transporters
L J Elsas, N Longo
Advances in Pediatrics
|
September 22, 1998
Human glucose transporters
N 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 fibroblasts
D J Danner, L J Elsas
Biochimica Et Biophysica Acta
|
March 17, 1972
Hexose transport and phosphorylation by hamster kidney cortex slices and averted jejunal rings
L J Elsas, R C Macdonell
Vitamins and Hormones
|
January 1, 1986
Genetic defects in vitamin utilization. Part I: General aspects and fat-solumbe vitamins
L J Elsas, D B McCormick
The Journal of Pediatrics
|
August 1, 1973
Familial glucose-galactose malabsorption: remission of glucose intolerance
L J Elsas, D W Lambe
Annals of the New York Academy of Sciences
|
January 1, 1982
The role of thiamin in maple syrup urine disease
L J Elsas, D J Danner
The Journal of Pediatrics
|
April 1, 1975
Classic phenylketonuria: diagnosis through heterozygote detection
R 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 disease
M L Wright, L J Elsas
Page
of 14