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Journal of Inherited Metabolic Disease|January 1, 1995
Impaired ketogenesis in fructose-1,6-bisphosphatase deficiency: a pitfall in the investigation of hypoglycaemiaA A Morris, S Deshphande, M P Ward-Platt, et al.Pediatric Nephrology (Berlin, Germany)|August 1, 1995
Neonatal Fanconi syndrome due to deficiency of complex III of the respiratory chainA A Morris, R W Taylor, M A Birch-Machin, et al.Journal of Hepatology|May 5, 1998
Liver failure associated with mitochondrial DNA depletionA A Morris, J W Taanman, J Blake, et al.The Journal of Pharmacology and Experimental Therapeutics|March 1, 1981
Effect of N-[(S)-1-carboxy-3-phenylpropyl]-L-Ala-L-Pro and its ethyl ester (MK-421) on angiotensin converting enzyme in vitro and angiotensin I pressor responses in vivoD M Gross, C S Sweet, E H Ulm, et al.Annals of Neurology|July 1, 1996
Deficiency of respiratory chain complex I is a common cause of Leigh diseaseA A Morris, J V Leonard, G K Brown, et al.Journal of Inherited Metabolic Disease|November 8, 2003
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiencyS E Olpin, A Afifi, S Clark, et al.Journal of Medical Genetics|March 3, 2009
Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and childrenJ D Stewart, S Tennant, H Powell, et al.Pageof 3