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Journal of Inherited Metabolic Disease
|
January 1, 1985
L-carnitine and glycine therapy in isovaleric acidaemia
R A Chalmers, C de Sousa, B M Tracey, et al.
The Journal of Biological Chemistry
|
May 25, 1992
Subunit molecular mass assignment of 14,654 Da to the soluble beta-galactoside-binding lectin from bovine heart muscle and demonstration of intramolecular disulfide bonding associated with oxidative inactivation
B M Tracey, T Feizi, W M Abbott, et al.
European Journal of Pediatrics
|
February 1, 1986
The response to L-carnitine and glycine therapy in isovaleric acidaemia
C de Sousa, R A Chalmers, T E Stacey, et al.
Archives of Disease in Childhood
|
November 1, 1983
Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups
C R Roe, C L Hoppel, T E Stacey, et al.
European Journal of Pediatrics
|
July 1, 1985
Dizygotic twins with 3-hydroxy-3-methylglutaric aciduria; unusual presentation, family studies and dietary management
T E Stacey, C de Sousa, B M Tracey, et al.
Lancet (London, England)
|
May 14, 1988
Contribution of gut bacterial metabolism to human metabolic disease
M D Bain, M Jones, S P Borriello, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
L-Carnitine insufficiency in disorders of organic acid metabolism: response to L-carnitine by patients with methylmalonic aciduria and 3-hydroxy-3-methylglutaric aciduria
R A Chalmers, T E Stacey, B M Tracey, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Experience with prenatal diagnosis of propionic acidaemia and methylmalonic aciduria
A H Fensom, P F Benson, R A Chalmers, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
The prenatal diagnosis of glutaric aciduria type II, using quantitative GC-MS
R A Chalmers, B M Tracey, G S King, et al.
Lancet (London, England)
|
April 14, 1984
Prenatal diagnosis of dysmorphic neonatal-lethal type II glutaricaciduria
J Boué, R A Chalmers, B M Tracey, et al.
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of 2
Search research articles
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Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Journal of Inherited Metabolic Disease
|
January 1, 1985
L-carnitine and glycine therapy in isovaleric acidaemia
R A Chalmers, C de Sousa, B M Tracey, et al.
The Journal of Biological Chemistry
|
May 25, 1992
Subunit molecular mass assignment of 14,654 Da to the soluble beta-galactoside-binding lectin from bovine heart muscle and demonstration of intramolecular disulfide bonding associated with oxidative inactivation
B M Tracey, T Feizi, W M Abbott, et al.
European Journal of Pediatrics
|
February 1, 1986
The response to L-carnitine and glycine therapy in isovaleric acidaemia
C de Sousa, R A Chalmers, T E Stacey, et al.
Archives of Disease in Childhood
|
November 1, 1983
Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups
C R Roe, C L Hoppel, T E Stacey, et al.
European Journal of Pediatrics
|
July 1, 1985
Dizygotic twins with 3-hydroxy-3-methylglutaric aciduria; unusual presentation, family studies and dietary management
T E Stacey, C de Sousa, B M Tracey, et al.
Lancet (London, England)
|
May 14, 1988
Contribution of gut bacterial metabolism to human metabolic disease
M D Bain, M Jones, S P Borriello, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
L-Carnitine insufficiency in disorders of organic acid metabolism: response to L-carnitine by patients with methylmalonic aciduria and 3-hydroxy-3-methylglutaric aciduria
R A Chalmers, T E Stacey, B M Tracey, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Experience with prenatal diagnosis of propionic acidaemia and methylmalonic aciduria
A H Fensom, P F Benson, R A Chalmers, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
The prenatal diagnosis of glutaric aciduria type II, using quantitative GC-MS
R A Chalmers, B M Tracey, G S King, et al.
Lancet (London, England)
|
April 14, 1984
Prenatal diagnosis of dysmorphic neonatal-lethal type II glutaricaciduria
J Boué, R A Chalmers, B M Tracey, et al.
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of 2