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M J Palmieri

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Analytical Biochemistry|May 1, 1991
The concentration of red blood cell UDPglucose and UDPgalactose determined by high-performance liquid chromatographyM J Palmieri, G T Berry, D A Player, et al.
The International Journal of Biochemistry|January 1, 1979
Heat and thyroxine sensitive isozymes of rat liver N-acetyl-beta-glucosaminidaseL V Oberkotter, C Horowitz, P M Coates, et al.
Analytical Biochemistry|April 1, 1992
31P NMR analysis of red blood cell UDPGlucose and UDPGalactose: comparison with HPLC and enzymatic methodsS L Wehrli, M J Palmieri, G T Berry, et al.
Enzyme & Protein|January 1, 1993
Concentration of white blood cell UDPgalactose and UDPglucose determined by high performance liquid chromatographyM J Palmieri, R A Reynolds, J B Gibson, et al.
Pediatric Research|November 1, 1994
Uridine diphosphate hexoses in leukocytes and fibroblasts of classic galactosemics and patients with other metabolic diseasesJ B Gibson, R A Reynolds, M J Palmieri, et al.
The American Journal of Clinical Nutrition|May 1, 1996
Sugar nucleotide concentrations in red blood cells of patients on protein- and lactose-limited diets: effect of galactose supplementationJ B Gibson, G T Berry, M J Palmieri, et al.
Biochemical and Molecular Medicine|June 1, 1995
Effect of glucose and galactose loading in normal subjects on red and white blood cell uridine diphosphate sugarsJ B Gibson, G T Berry, A T Mazur, et al.
The New England Journal of Medicine|January 17, 1991
Branched-chain amino acid-free parenteral nutrition in the treatment of acute metabolic decompensation in patients with maple syrup urine diseaseG T Berry, R Heidenreich, P Kaplan, et al.
Journal of Inherited Metabolic Disease|January 5, 2002
Neonatal hypoglycaemia in severe succinyl-CoA: 3-oxoacid CoA-transferase deficiencyG T Berry, T Fukao, G A Mitchell, et al.
Metabolism: Clinical and Experimental|May 1, 1995
Comparison of erythrocyte uridine sugar nucleotide levels in normals, classic galactosemics, and patients with other metabolic disordersJ B Gibson, R A Reynolds, M J Palmieri, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Analytical Biochemistry|May 1, 1991
The concentration of red blood cell UDPglucose and UDPgalactose determined by high-performance liquid chromatographyM J Palmieri, G T Berry, D A Player, et al.
The International Journal of Biochemistry|January 1, 1979
Heat and thyroxine sensitive isozymes of rat liver N-acetyl-beta-glucosaminidaseL V Oberkotter, C Horowitz, P M Coates, et al.
Analytical Biochemistry|April 1, 1992
31P NMR analysis of red blood cell UDPGlucose and UDPGalactose: comparison with HPLC and enzymatic methodsS L Wehrli, M J Palmieri, G T Berry, et al.
Enzyme & Protein|January 1, 1993
Concentration of white blood cell UDPgalactose and UDPglucose determined by high performance liquid chromatographyM J Palmieri, R A Reynolds, J B Gibson, et al.
Pediatric Research|November 1, 1994
Uridine diphosphate hexoses in leukocytes and fibroblasts of classic galactosemics and patients with other metabolic diseasesJ B Gibson, R A Reynolds, M J Palmieri, et al.
The American Journal of Clinical Nutrition|May 1, 1996
Sugar nucleotide concentrations in red blood cells of patients on protein- and lactose-limited diets: effect of galactose supplementationJ B Gibson, G T Berry, M J Palmieri, et al.
Biochemical and Molecular Medicine|June 1, 1995
Effect of glucose and galactose loading in normal subjects on red and white blood cell uridine diphosphate sugarsJ B Gibson, G T Berry, A T Mazur, et al.
The New England Journal of Medicine|January 17, 1991
Branched-chain amino acid-free parenteral nutrition in the treatment of acute metabolic decompensation in patients with maple syrup urine diseaseG T Berry, R Heidenreich, P Kaplan, et al.
Journal of Inherited Metabolic Disease|January 5, 2002
Neonatal hypoglycaemia in severe succinyl-CoA: 3-oxoacid CoA-transferase deficiencyG T Berry, T Fukao, G A Mitchell, et al.
Metabolism: Clinical and Experimental|May 1, 1995
Comparison of erythrocyte uridine sugar nucleotide levels in normals, classic galactosemics, and patients with other metabolic disordersJ B Gibson, R A Reynolds, M J Palmieri, et al.
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