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European Journal of Pediatrics
|
March 1, 1990
In vivo propionate oxidation as a prognostic indicator in disorders of propionate metabolism
G N Thompson, J H Walter, J L Bresson, et al.
European Journal of Pediatrics
|
October 12, 2013
Unsuccessful treatment of severe pyruvate carboxylase deficiency with triheptanoin
C Breen, F J White, C A B Scott, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
A simple isotopic technique for assessing vitamin responsiveness in vivo in propionic acidaemia
G N Thompson, J L Bresson, J P Bonnefont, et al.
The American Journal of Physiology
|
April 1, 1990
Protein and leucine metabolism in maple syrup urine disease
G N Thompson, J L Bresson, P J Pacy, et al.
Developmental Medicine and Child Neurology
|
August 15, 2006
Pyruvate dehydrogenase E3 binding protein (protein X) deficiency
R M Brown, R A Head, A A M Morris, et al.
Lancet (London, England)
|
July 13, 2002
How practical are recommendations for dietary control in phenylketonuria?
J H Walter, F J White, S K Hall, et al.
Developmental Medicine and Child Neurology
|
October 12, 2004
Pyruvate dehydrogenase deficiency presenting as dystonia in childhood
R A Head, C G E L de Goede, R W N Newton, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
December 18, 2001
Vascular outcome in patients with homocystinuria due to cystathionine beta-synthase deficiency treated chronically: a multicenter observational study
S Yap, G H Boers, B Wilcken, et al.
Metabolism: Clinical and Experimental
|
November 1, 1990
Sources of propionate in inborn errors of propionate metabolism
G N Thompson, J H Walter, J L Bresson, et al.
The Journal of Pediatrics
|
November 1, 1989
Substrate disposal in metabolic disease: a comparison between rates of in vivo propionate oxidation and urinary metabolite excretion in children with methylmalonic acidemia
G N Thompson, J H Walter, J L Bresson, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 96) with videos related to
Sort By:
Page
of 10
European Journal of Pediatrics
|
March 1, 1990
In vivo propionate oxidation as a prognostic indicator in disorders of propionate metabolism
G N Thompson, J H Walter, J L Bresson, et al.
European Journal of Pediatrics
|
October 12, 2013
Unsuccessful treatment of severe pyruvate carboxylase deficiency with triheptanoin
C Breen, F J White, C A B Scott, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
A simple isotopic technique for assessing vitamin responsiveness in vivo in propionic acidaemia
G N Thompson, J L Bresson, J P Bonnefont, et al.
The American Journal of Physiology
|
April 1, 1990
Protein and leucine metabolism in maple syrup urine disease
G N Thompson, J L Bresson, P J Pacy, et al.
Developmental Medicine and Child Neurology
|
August 15, 2006
Pyruvate dehydrogenase E3 binding protein (protein X) deficiency
R M Brown, R A Head, A A M Morris, et al.
Lancet (London, England)
|
July 13, 2002
How practical are recommendations for dietary control in phenylketonuria?
J H Walter, F J White, S K Hall, et al.
Developmental Medicine and Child Neurology
|
October 12, 2004
Pyruvate dehydrogenase deficiency presenting as dystonia in childhood
R A Head, C G E L de Goede, R W N Newton, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
December 18, 2001
Vascular outcome in patients with homocystinuria due to cystathionine beta-synthase deficiency treated chronically: a multicenter observational study
S Yap, G H Boers, B Wilcken, et al.
Metabolism: Clinical and Experimental
|
November 1, 1990
Sources of propionate in inborn errors of propionate metabolism
G N Thompson, J H Walter, J L Bresson, et al.
The Journal of Pediatrics
|
November 1, 1989
Substrate disposal in metabolic disease: a comparison between rates of in vivo propionate oxidation and urinary metabolite excretion in children with methylmalonic acidemia
G N Thompson, J H Walter, J L Bresson, et al.
Page
of 10