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S D Cederbaum

Showing results (41-50 of 93) with videos related to

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Neurology|July 1, 1975
Familial poliodystrophy, mitochondrial myopathy, and lactate acidemiaY Shapira, S D Cederbaum, P A Cancilla, et al.
The New England Journal of Medicine|March 14, 1974
Letter: Priapism after phenoxybenzamine in a patient with Fabry's diseaseS J Funderburk, M Philippart, G Dale, et al.
The Journal of Pediatrics|August 1, 1979
Hyperlysinemia with saccharopinuria due to combined lysine-ketoglutarate reductase and saccharopine dehydrogenase deficiencies presenting as cystinuriaS D Cederbaum, K N Shaw, J Dancis, et al.
Biochemical Medicine|October 1, 1982
Biochemical properties of arginase in human adult and fetal tissuesE B Spector, S C Rice, S Moedjono, et al.
The Journal of Pediatrics|January 10, 2001
Psychosocial issues and coping strategies in families affected by urea cycle disordersJ A Cederbaum, C LeMons, M Rosen, et al.
Biochimica Et Biophysica Acta|July 20, 1981
Microinjection of arginase into enzyme-deficient cells with the isolated glycoproteins of Sendai virus as fusogenC A Kruse, E B Spector, S D Cederbaum, et al.
Somatic Cell and Molecular Genetics|July 1, 1991
Effect of an adjacent base on detection of a point mutation by restriction enzyme digestionD Klein, A E Dodson, D E Tabor, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Menstrual cycle and gonadal steroid effects on symptomatic hyperammonaemia of urea-cycle-based and idiopathic aetiologiesW W Grody, R J Chang, N M Panagiotis, et al.
The Journal of Pediatrics|December 1, 1978
Methylmalonyl-CoA mutase deficiency associated with severe neonatal hyperammonemia: activity of urea cycle enzymesL J Shapiro, M E Bocian, L Raijman, et al.
Archives of Biochemistry and Biophysics|February 10, 2000
Induction of arginase II in human Caco-2 tumor cells by cyclic AMPL H Wei, S M Morris, S D Cederbaum, et al.
Pageof 10

Showing results (41-50 of 93) with videos related to

Sort By:
Pageof 10
Neurology|July 1, 1975
Familial poliodystrophy, mitochondrial myopathy, and lactate acidemiaY Shapira, S D Cederbaum, P A Cancilla, et al.
The New England Journal of Medicine|March 14, 1974
Letter: Priapism after phenoxybenzamine in a patient with Fabry's diseaseS J Funderburk, M Philippart, G Dale, et al.
The Journal of Pediatrics|August 1, 1979
Hyperlysinemia with saccharopinuria due to combined lysine-ketoglutarate reductase and saccharopine dehydrogenase deficiencies presenting as cystinuriaS D Cederbaum, K N Shaw, J Dancis, et al.
Biochemical Medicine|October 1, 1982
Biochemical properties of arginase in human adult and fetal tissuesE B Spector, S C Rice, S Moedjono, et al.
The Journal of Pediatrics|January 10, 2001
Psychosocial issues and coping strategies in families affected by urea cycle disordersJ A Cederbaum, C LeMons, M Rosen, et al.
Biochimica Et Biophysica Acta|July 20, 1981
Microinjection of arginase into enzyme-deficient cells with the isolated glycoproteins of Sendai virus as fusogenC A Kruse, E B Spector, S D Cederbaum, et al.
Somatic Cell and Molecular Genetics|July 1, 1991
Effect of an adjacent base on detection of a point mutation by restriction enzyme digestionD Klein, A E Dodson, D E Tabor, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Menstrual cycle and gonadal steroid effects on symptomatic hyperammonaemia of urea-cycle-based and idiopathic aetiologiesW W Grody, R J Chang, N M Panagiotis, et al.
The Journal of Pediatrics|December 1, 1978
Methylmalonyl-CoA mutase deficiency associated with severe neonatal hyperammonemia: activity of urea cycle enzymesL J Shapiro, M E Bocian, L Raijman, et al.
Archives of Biochemistry and Biophysics|February 10, 2000
Induction of arginase II in human Caco-2 tumor cells by cyclic AMPL H Wei, S M Morris, S D Cederbaum, et al.
Pageof 10