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The American Journal of Physiology|April 1, 1990
Protein and leucine metabolism in maple syrup urine diseaseG 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) deficiencyR 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.
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 studyS Yap, G H Boers, B Wilcken, et al.
Developmental Medicine and Child Neurology|October 12, 2004
Pyruvate dehydrogenase deficiency presenting as dystonia in childhoodR A Head, C G E L de Goede, R W N Newton, et al.
Metabolism: Clinical and Experimental|November 1, 1990
Sources of propionate in inborn errors of propionate metabolismG N Thompson, J H Walter, J L Bresson, et al.
European Journal of Pediatrics|August 1, 1990
The use of metronidazole in management of methylmalonic and propionic acidaemiasG N Thompson, R A Chalmers, J H Walter, 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 acidemiaG N Thompson, J H Walter, J L Bresson, et al.
Lancet (London, England)|December 10, 1994
Maternal mild hyperphenylalaninaemia: an international survey of offspring outcomeH L Levy, S E Waisbren, D Lobbregt, et al.
Orphanet Journal of Rare Diseases|October 14, 2017
The complete European guidelines on phenylketonuria: diagnosis and treatmentA M J van Wegberg, A MacDonald, K Ahring, et al.
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