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Archives of Disease in Childhood|November 1, 1992
Intercurrent illness in inborn errors of intermediary metabolismM A Dixon, J V LeonardArchives of Disease in Childhood|June 1, 1996
Uncooked cornstarch--efficacy in type I glycogenosisP J Lee, M A Dixon, J V LeonardThe Journal of Pediatrics|May 10, 2000
Resting energy expenditure in disorders of propionate metabolismF Feillet, O A Bodamer, M A Dixon, et al.Journal of Inherited Metabolic Disease|September 16, 2003
What is the role of medium-chain triglycerides in the management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency?A M Lund, M A Dixon, P Vreken, et al.Journal of Inherited Metabolic Disease|September 16, 2003
Plasma and erythrocyte fatty acid concentrations in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyA M Lund, M A Dixon, P Vreken, et al.Annals of Clinical Biochemistry|March 1, 1975
An assessment of the performance of the SMA 12/micro autoanalyser in clinical useJ V LeonardThe Journal of Pediatrics|January 10, 2001
The nutritional management of urea cycle disordersJ V LeonardJournal of Inherited Metabolic Disease|June 10, 2006
Komrower lecture: Treatment of inborn errors of metabolism: a reviewJ V LeonardJournal of Inherited Metabolic Disease|January 1, 1995
The management and outcome of propionic and methylmalonic acidaemiaJ V LeonardJournal of Inherited Metabolic Disease|May 4, 2005
Acute metabolic encephalopathy: an introductionJ V LeonardPageof 21