M. P. Champion

Neonatal epileptic encephalopathy caused by mutations in the PNPO gene encoding pyridox(am)ine 5′-phosphate oxidase

Philippa B. Mills, Robert Surtees, M. P. Champion et al. · Human Molecular Genetics · 2005 · 307 citations · Full text

Hepatocyte Transplantation Followed by Auxiliary Liver Transplantation—a Novel Treatment for Ornithine Transcarbamylase Deficiency

Juliana Puppi, N. Tan, Ragai R. Mitry et al. · American Journal of Transplantation · 2008 · 115 citations · Full text

Serum lactate as a predictor of mortality after paediatric cardiac surgery

Mark Hatherill, Tina Sajjanhar, SM Tibby et al. · Archives of Disease in Childhood · 1997 · 115 citations · Full text

High frequency of missense mutations in glycogen storage disease type VI

Nicholas Beauchamp, Joanna Taybert, M. P. Champion et al. · Journal of Inherited Metabolic Disease · 2007 · 56 citations · Full text

The Birth Prevalence of PKU in Populations of European, South Asian and Sub‐Saharan African Ancestry Living in South East England

Pia Hardelid, Mario Cortina‐Borja, Alastair Munro et al. · Annals of Human Genetics · 2007 · 56 citations

Birth Prevalence, Human Pah Locus, Genetic Disorder +13