Marcus Oppenheim

Pyridoxal 5'-phosphate in cerebrospinal fluid; factors affecting concentration

P. Clayton, S. Heales, P. Mills, 2011, Journal of Inherited Metabolic Disease.

Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency

T. Meitinger, T. Strom, H. Prokisch, 2016, American journal of human genetics.

Measurement of plasma B6 vitamer profiles in children with inborn errors of vitamin B6 metabolism using an LC-MS/MS method

K. Mills, P. Clayton, S. Heales, 2013, Journal of Inherited Metabolic Disease.

Pyridoxal 5′‐phosphate deficiency causes a loss of aromatic l‐amino acid decarboxylase in patients and human neuroblastoma cells, implications for aromatic l‐amino acid decarboxylase and vitamin B6 deficiency states

P. Clayton, P. Clayton, J. Fitzgerald, 2010, Journal of neurochemistry.

Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2

S. Züchner, M. Lek, F. Muntoni, 2013, Brain : a journal of neurology.

Combined HPLC Analysis of 25-OH-Vitamin D 3 and D 2 Product information Page 3 / 4 Reference values for vitamin B 1 and vitamin B 6 in whole blood

G. Steen, J. Rajah, L. Abdel-Wareth, 2007 .

Pyridoxal 5'-phosphate values in cerebrospinal fluid: reference values and diagnosis of PNPO deficiency in paediatric patients.

Rafael Artuch, Aida Ormazabal, Keith Hyland, 2008, Molecular genetics and metabolism.

Coenzyme Q10 and Pyridoxal Phosphate Deficiency Is a Common Feature in Mucopolysaccharidosis Type III.

P. Navas, P. Clayton, R. Artuch, 2015, JIMD reports.