Peter T. Clayton
Biochemistry
Endocrinology and Metabolism Unit
Institute of Child Health
University College London
U.K
Name/email consistency: high
- B6-responsive disorders: a model of vitamin dependency. Clayton, P.T. J. Inherit. Metab. Dis. (2006)
- Neonatal epileptic encephalopathy. Clayton, P.T., Surtees, R.A., DeVile, C., Hyland, K., Heales, S.J. Lancet (2003)
- Inborn errors presenting with liver dysfunction. Clayton, P.T. Semin. Neonatol (2002)
- 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)
- Clinical consequences of defects in peroxisomal beta-oxidation. Clayton, P.T. Biochem. Soc. Trans. (2001)
- Applications of mass spectrometry in the study of inborn errors of metabolism. Clayton, P.T. J. Inherit. Metab. Dis. (2001)
- 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)
- 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)