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British 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 LeeArchives of Disease in Childhood|September 1, 1978
Case of tumour ricketsM W Moncrieff, D P Brenton, L J ArthurAnnals of Human Genetics|January 1, 1980
Changes in the activity and isozyme patterns of glycolytic enzymes during stimulation of normal human lymphocytes with phytohaemagglutininP A Rogers, D P Brenton, D A HopkinsonArchives of Disease in Childhood|March 1, 1980
Renal tubular acidosis and nerve deafnessD B Dunger, D P Brenton, A R CainJournal of Neurology, Neurosurgery, and Psychiatry|June 1, 1987
Neurological involvement in X-linked hypophosphataemic ricketsP G Bradbury, D P Brenton, G M SternJournal of Inherited Metabolic Disease|March 14, 2007
A practical approach to maternal phenylketonuria managementF Maillot, P Cook, M Lilburn, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1988
Dystonia in homocystinuriaP A Kempster, D P Brenton, A N Gale, et al.Journal of Inherited Metabolic Disease|January 1, 1986
Glycerol-3-phosphate excretion in fructose-1,6-diphosphatase deficiencyS Krywawych, G Katz, A M Lawson, et al.American Journal of Medical Genetics|January 1, 1987
DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): elevated plasma and urinary 2-oxoglutarate in three unrelated patientsM A Patton, S Krywawych, R M Winter, et al.Pageof 4