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Archives of Disease in Childhood|June 1, 1996
Uncooked cornstarch--efficacy in type I glycogenosisP J Lee, M A Dixon, J V LeonardArchives of Disease in Childhood|November 1, 1992
Intercurrent illness in inborn errors of intermediary metabolismM A Dixon, J V LeonardJournal of Inherited Metabolic Disease|January 1, 1995
The hepatic glycogen storage diseases--problems beyond childhoodP J Lee, J V LeonardJournal of Inherited Metabolic Disease|January 24, 2002
Plasma glutamine and ammonia concentrations in ornithine carbamoyltransferase deficiency and citrullinaemiaC J Wilson, P J Lee, 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.Journal of Inherited Metabolic Disease|December 22, 1999
Blood lipids and endothelial function in glycogen storage disease type IIIE Hershkovitz, A Donald, M Mullen, et al.Pediatric Nephrology (Berlin, Germany)|December 1, 1995
Glomerular and tubular function in glycogen storage diseaseP J Lee, R N Dalton, V Shah, et al.European Journal of Pediatrics|June 1, 1995
Bone mineralisation in type 1 glycogen storage diseaseP J Lee, J S Patel, M Fewtrell, et al.Pageof 30