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European Journal of Pediatrics|July 1, 1996
Maternal phenylketonuria. A study from the United KingdomD P Brenton, M LilburnBritish Medical Journal|May 21, 1977
25-Hydroxycholecalciferol absorption in steatorrhoea and postgastrectomy osteomalaciaJ M Gertner, M Lilburn, M DomenechJournal of Inherited Metabolic Disease|September 10, 2005
A new protein substitute for adolescents and adults with maple syrup urine disease (MSUD)P Hallam, M Lilburn, P J LeeJournal of Inherited Metabolic Disease|March 14, 2007
A practical approach to maternal phenylketonuria managementF Maillot, P Cook, M Lilburn, et al.European Journal of Pediatrics|July 1, 1996
Phenylketonuria: treatment in adolescence and adult lifeD P Brenton, A C Tarn, J C Cabrera-Abreu, et al.Journal of Applied Microbiology|August 21, 2010
Use of bioluminescence imaging to monitor Campylobacter survival in chicken litterI I Kassem, Y Sanad, D Gangaiah, et al.Journal of Inherited Metabolic Disease|April 8, 2006
Neuropsychometric outcome predictors for adults with maple syrup urine diseaseC le Roux, E Murphy, P Hallam, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 11, 2009
Adults with late diagnosed PKU and severe challenging behaviour: a randomised placebo-controlled trial of a phenylalanine-restricted dietP J Lee, A Amos, L Robertson, et al.Journal of Inherited Metabolic Disease|June 1, 2006
'Ready to drink' protein substitute is easier is for people with phenylketonuriaA MacDonald, M Lilburn, P Davies, et al.Journal of Inherited Metabolic Disease|October 23, 2008
Long-term compliance with a novel vitamin and mineral supplement in older people with PKUA MacDonald, P Lee, P Davies, et al.Pageof 2