H. Lemonde

Performance of laboratory tests used to measure blood phenylalanine for the monitoring of patients with phenylketonuria

J. Bonham, C. Weykamp, J. Mei, 2020, Journal of inherited metabolic disease.

A new method for the rapid diagnosis of protein N-linked congenital disorders of glycosylation.

W. Heywood, K. Mills, P. Clayton, 2013, Journal of proteome research.

Mutations in SRD5B1 (AKR1D1), the gene encoding delta(4)-3-oxosteroid 5beta-reductase, in hepatitis and liver failure in infancy.

P. Scambler, M. Durán, P. Clayton, 2003, Gut.

Inherited Metabolic Disorders and the Liver

M. Champion, H. Lemonde, 2016 .

The identification of unusual bile acid metabolites by tandem mass spectrometry: use of low-energy collision-induced dissociation to produce informative spectra.

P. Clayton, A. Johnson, H. Lemonde, 1999, Rapid communications in mass spectrometry : RCM.

Disorders of Bile Acid Synthesis and Biliary Transport

P. Clayton, P. Gissen, H. Lemonde, 2014 .

Optimisation of Bile Production during Normothermic Preservation of Porcine Livers

P. Friend, S. S. St. Peter, A. Butler, 2002, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency

Robert W. Taylor, Courtney E. French, A. Pagnamenta, 2018, American Journal of Human Genetics.

Inherited mitochondrial disease

S. Rahman, H. Lemonde, 2015, Paediatrics and Child Health.

Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency.

P. Vreken, R. Wanders, J. Adamski, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Newborn screening for inborn errors of metabolism

A. Chakrapani, M. Cleary, H. Lemonde, 2015 .