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Placenta
|
July 1, 1987
Cytosolic fatty acid binding proteins in rat placenta
R Brandes, R Arad, V Barash
Enzyme
|
January 1, 1988
Pyruvate carboxylase activity in chorionic villi: possibility of application to prenatal diagnosis
V Barash, S Khassis, M Granat, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Apparent absence of glycogen branching enzyme activity in phosphofructokinase deficiency
V Barash, S Lilling, R Fischer, et al.
Brain Research
|
June 3, 1985
Effect of L-DOPA on glucose oxidation and incorporation into glycogen in discrete brain regions of the rat
V Barash, M Globus, E Melamed, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: biochemical studies and family investigation of four generations
V Barash, H Mandel, S Sella, et al.
Placenta
|
March 1, 1987
Localization of glycogen in the placenta of diabetic rats: a light and electron microscopic study
Z Ne'eman, V Barash, E Rosenmann, et al.
American Journal of Diseases of Children (1960)
|
February 1, 1989
Fructose-1,6-diphosphatase deficiency: a 20-year follow-up
O N Elpeleg, V Barash, H Hurvitz, et al.
Neurology
|
June 1, 1994
Late-onset muscular weakness in phosphofructokinase deficiency due to exon 5/intron 5 junction point mutation: a unique disorder or the natural course of this glycolytic disorder?
Z Argov, V Barash, D Soffer, et al.
Pediatric Neurology
|
September 1, 1988
Ring 18 chromosome with mental retardation, hemidysmorphism, and mitochondrial encephalomyopathy
R Amit, A Gutman, R Udassin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 1, 1988
Familial carnitine deficiency: further evidence for autosomal recessive transmission with variable expression
E Shahar, N Brand, Y Shapira, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 56) with videos related to
Sort By:
Page
of 6
Placenta
|
July 1, 1987
Cytosolic fatty acid binding proteins in rat placenta
R Brandes, R Arad, V Barash
Enzyme
|
January 1, 1988
Pyruvate carboxylase activity in chorionic villi: possibility of application to prenatal diagnosis
V Barash, S Khassis, M Granat, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Apparent absence of glycogen branching enzyme activity in phosphofructokinase deficiency
V Barash, S Lilling, R Fischer, et al.
Brain Research
|
June 3, 1985
Effect of L-DOPA on glucose oxidation and incorporation into glycogen in discrete brain regions of the rat
V Barash, M Globus, E Melamed, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: biochemical studies and family investigation of four generations
V Barash, H Mandel, S Sella, et al.
Placenta
|
March 1, 1987
Localization of glycogen in the placenta of diabetic rats: a light and electron microscopic study
Z Ne'eman, V Barash, E Rosenmann, et al.
American Journal of Diseases of Children (1960)
|
February 1, 1989
Fructose-1,6-diphosphatase deficiency: a 20-year follow-up
O N Elpeleg, V Barash, H Hurvitz, et al.
Neurology
|
June 1, 1994
Late-onset muscular weakness in phosphofructokinase deficiency due to exon 5/intron 5 junction point mutation: a unique disorder or the natural course of this glycolytic disorder?
Z Argov, V Barash, D Soffer, et al.
Pediatric Neurology
|
September 1, 1988
Ring 18 chromosome with mental retardation, hemidysmorphism, and mitochondrial encephalomyopathy
R Amit, A Gutman, R Udassin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 1, 1988
Familial carnitine deficiency: further evidence for autosomal recessive transmission with variable expression
E Shahar, N Brand, Y Shapira, et al.
Page
of 6