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Peter T. Clayton


Endocrinology and Metabolism Unit

Institute of Child Health

University College London



Name/email consistency: high



  • Biochemistry, Endocrinology and Metabolism Unit, Institute of Child Health, University College London, U.K. 2001 - 2006
  • Department of Metabolic Medicine, Great Ormond Street Hospital for Children, WC1N 1EH, London, UK. 2003
  • London Centre for Paediatric Endocrinology and Metabolism, Biochemistry, Endocrinology and Metabolism Unit, Institute of Child Health, United Kingdom. 2001
  • Institute of Child Health, University College London, UK. 1998


  1. B6-responsive disorders: a model of vitamin dependency. Clayton, P.T. J. Inherit. Metab. Dis. (2006) [Pubmed]
  2. Neonatal epileptic encephalopathy. Clayton, P.T., Surtees, R.A., DeVile, C., Hyland, K., Heales, S.J. Lancet (2003) [Pubmed]
  3. Inborn errors presenting with liver dysfunction. Clayton, P.T. Semin. Neonatol (2002) [Pubmed]
  4. Mutations in the sterol 27-hydroxylase gene (CYP27A) cause hepatitis of infancy as well as cerebrotendinous xanthomatosis. Clayton, P.T., Verrips, A., Sistermans, E., Mann, A., Mieli-Vergani, G., Wevers, R. J. Inherit. Metab. Dis. (2002) [Pubmed]
  5. Clinical consequences of defects in peroxisomal beta-oxidation. Clayton, P.T. Biochem. Soc. Trans. (2001) [Pubmed]
  6. Applications of mass spectrometry in the study of inborn errors of metabolism. Clayton, P.T. J. Inherit. Metab. Dis. (2001) [Pubmed]
  7. Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion. Clayton, P.T., Eaton, S., Aynsley-Green, A., Edginton, M., Hussain, K., Krywawych, S., Datta, V., Malingre, H.E., Berger, R., van den Berg, I.E. J. Clin. Invest. (2001) [Pubmed]
  8. Screening for medium chain acyl-CoA dehydrogenase deficiency using electrospray ionisation tandem mass spectrometry. Clayton, P.T., Doig, M., Ghafari, S., Meaney, C., Taylor, C., Leonard, J.V., Morris, M., Johnson, A.W. Arch. Dis. Child. (1998) [Pubmed]
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