C.J. Wilson
Metabolic Unit
Great Ormond Street Hospital for Children
Great Ormond Street
London WC1N 3JH
UK
Name/email consistency: high
- Autosomal recessive osteopetrosis: diagnosis, management, and outcome. Wilson, C.J., Vellodi, A. Arch. Dis. Child. (2000)
- Phenylalanine supplementation improves the phenylalanine profile in tyrosinaemia. Wilson, C.J., Van Wyk, K.G., Leonard, J.V., Clayton, P.T. J. Inherit. Metab. Dis. (2000)
- Mitochondrial DNA point mutation T9176C in Leigh syndrome. Wilson, C.J., Wood, N.W., Leonard, J.V., Surtees, R., Rahman, S. J. Child Neurol. (2000)
- Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosis. Wilson, C.J., Champion, M.P., Collins, J.E., Clayton, P.T., Leonard, J.V. Arch. Dis. Child. (1999)