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Neurology
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July 1, 1975
Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia
Y 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 disease
S 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 cystinuria
S D Cederbaum, K N Shaw, J Dancis, et al.
Biochemical Medicine
|
October 1, 1982
Biochemical properties of arginase in human adult and fetal tissues
E 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 disorders
J 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 fusogen
C 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 digestion
D 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 aetiologies
W 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 enzymes
L 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 AMP
L H Wei, S M Morris, S D Cederbaum, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 93) with videos related to
Sort By:
Page
of 10
Neurology
|
July 1, 1975
Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia
Y 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 disease
S 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 cystinuria
S D Cederbaum, K N Shaw, J Dancis, et al.
Biochemical Medicine
|
October 1, 1982
Biochemical properties of arginase in human adult and fetal tissues
E 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 disorders
J 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 fusogen
C 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 digestion
D 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 aetiologies
W 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 enzymes
L 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 AMP
L H Wei, S M Morris, S D Cederbaum, et al.
Page
of 10