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M Brivet

Showing results (1-10 of 48) with videos related to

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Annales De Biologie Clinique|January 1, 1979
[Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)]M Brivet, N Moatti, A Lemonnier
Gastroenterologie Clinique Et Biologique|November 1, 1984
[Occurrence and nature of hyperamylasemia in chronic alcoholics]G Pelletier, N Née, M Brivet, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 30, 1988
The Philadelphia variant of galactokinase in human erythrocytes: physicochemical and catalytic propertiesT Soni, M Brivet, N Moatti, et al.
Journal of Inherited Metabolic Disease|October 13, 2001
Partial effect of bromocriptine on lactose and galactose synthesis in a pregnant woman heterozygous for galactosaemiaM Odièvre, M Brivet, M F Rivière, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 13, 1988
The Philadelphia variant of galactokinase: impaired [1-14C]galactose oxidation by intact erythrocytesT Soni, M Brivet, N Moatti, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1994
Low efficiency of [14C]galactose incorporation by galactosemic skin fibroblasts: relationship with neurological sequelaeN Kadhom, J Baptista, M Brivet, et al.
Biochemical Genetics|April 1, 1989
Cytosolic thymidine kinase activity in cultured human fibroblasts from individuals with galactokinase deficiencyJ Baptista, M Brivet, N Kadhom, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]|February 1, 1979
Study of some enzymatic activities in human liver cell culturesF Lemonnier, N Moatti, M Brivet, et al.
Molecular Genetics and Metabolism|February 3, 2000
Evidence for a short-chain carnitine-acylcarnitine translocase in mitochondria specifically related to the metabolism of branched-chain amino acidsD S Roe, C R Roe, M Brivet, et al.
Pediatric Research|February 1, 1983
Defective galactose oxidation in a patient with glycogen storage disease and Fanconi syndromeM Brivet, N Moatti, A Corriat, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Annales De Biologie Clinique|January 1, 1979
[Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)]M Brivet, N Moatti, A Lemonnier
Gastroenterologie Clinique Et Biologique|November 1, 1984
[Occurrence and nature of hyperamylasemia in chronic alcoholics]G Pelletier, N Née, M Brivet, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 30, 1988
The Philadelphia variant of galactokinase in human erythrocytes: physicochemical and catalytic propertiesT Soni, M Brivet, N Moatti, et al.
Journal of Inherited Metabolic Disease|October 13, 2001
Partial effect of bromocriptine on lactose and galactose synthesis in a pregnant woman heterozygous for galactosaemiaM Odièvre, M Brivet, M F Rivière, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 13, 1988
The Philadelphia variant of galactokinase: impaired [1-14C]galactose oxidation by intact erythrocytesT Soni, M Brivet, N Moatti, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1994
Low efficiency of [14C]galactose incorporation by galactosemic skin fibroblasts: relationship with neurological sequelaeN Kadhom, J Baptista, M Brivet, et al.
Biochemical Genetics|April 1, 1989
Cytosolic thymidine kinase activity in cultured human fibroblasts from individuals with galactokinase deficiencyJ Baptista, M Brivet, N Kadhom, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]|February 1, 1979
Study of some enzymatic activities in human liver cell culturesF Lemonnier, N Moatti, M Brivet, et al.
Molecular Genetics and Metabolism|February 3, 2000
Evidence for a short-chain carnitine-acylcarnitine translocase in mitochondria specifically related to the metabolism of branched-chain amino acidsD S Roe, C R Roe, M Brivet, et al.
Pediatric Research|February 1, 1983
Defective galactose oxidation in a patient with glycogen storage disease and Fanconi syndromeM Brivet, N Moatti, A Corriat, et al.
Pageof 5