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R D Scholem

Showing results (1-10 of 9) with videos related to

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The Biochemical Journal|October 15, 1983
Metabolism of malonic semialdehyde in manR D Scholem, G K Brown
Journal of Inherited Metabolic Disease|January 1, 1984
Malonyl coenzyme A decarboxylase deficiencyG K Brown, R D Scholem, A Bankier, et al.
The Biochemical Journal|October 1, 1986
Immunochemical analysis of normal and mutant forms of human pyruvate dehydrogenaseC A Wicking, R D Scholem, S M Hunt, et al.
European Journal of Pediatrics|April 1, 1986
Malonyl coenzyme A decarboxylase deficiency. Clinical and biochemical findings in a second child with a more severe enzyme defectE A Haan, R D Scholem, H B Croll, et al.
European Journal of Pediatrics|September 1, 1987
Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduriaE A Haan, R D Scholem, J J Pitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Hyperammonaemia and lactic acidosis in a patient with pyruvate dehydrogenase deficiencyG K Brown, R D Scholem, S M Hunt, et al.
Neurology|February 1, 1989
Sulfite oxidase deficiency: clinical, neuroradiologic, and biochemical features in two new patientsG K Brown, R D Scholem, H B Croll, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Deoxyribose-5-phosphate aldolase deficiency--a harmless inborn error of metabolismA Chappel, R D Scholem, G K Brown, et al.
European Journal of Pediatrics|January 1, 1988
"Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosisG K Brown, E A Haan, D M Kirby, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
The Biochemical Journal|October 15, 1983
Metabolism of malonic semialdehyde in manR D Scholem, G K Brown
Journal of Inherited Metabolic Disease|January 1, 1984
Malonyl coenzyme A decarboxylase deficiencyG K Brown, R D Scholem, A Bankier, et al.
The Biochemical Journal|October 1, 1986
Immunochemical analysis of normal and mutant forms of human pyruvate dehydrogenaseC A Wicking, R D Scholem, S M Hunt, et al.
European Journal of Pediatrics|April 1, 1986
Malonyl coenzyme A decarboxylase deficiency. Clinical and biochemical findings in a second child with a more severe enzyme defectE A Haan, R D Scholem, H B Croll, et al.
European Journal of Pediatrics|September 1, 1987
Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduriaE A Haan, R D Scholem, J J Pitt, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Hyperammonaemia and lactic acidosis in a patient with pyruvate dehydrogenase deficiencyG K Brown, R D Scholem, S M Hunt, et al.
Neurology|February 1, 1989
Sulfite oxidase deficiency: clinical, neuroradiologic, and biochemical features in two new patientsG K Brown, R D Scholem, H B Croll, et al.
Journal of Inherited Metabolic Disease|January 1, 1983
Deoxyribose-5-phosphate aldolase deficiency--a harmless inborn error of metabolismA Chappel, R D Scholem, G K Brown, et al.
European Journal of Pediatrics|January 1, 1988
"Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosisG K Brown, E A Haan, D M Kirby, et al.
Pageof 1