James R. Bonham

Phosphoserine Aminotransferase Deficiency: A Novel Disorder of the Serine Biosynthesis Pathway

Claire Hart, Valérie Race, Younès Achouri et al. · The American Journal of Human Genetics · 2007 · 131 citations · Full text

Biosynthesis, Phosphoserine Aminotransferase Deficiency, Cellular Enzymology +9

Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiency

S. E. Olpin, S. Clark, Brage Storstein Andresen et al. · Journal of Inherited Metabolic Disease · 2004 · 74 citations

An indirect response model of homocysteine suppression by betaine: optimising the dosage regimen of betaine in homocystinuria

Angela Matthews, Trevor N. Johnson, Amin Rostami‐Hodjegan et al. · British Journal of Clinical Pharmacology · 2002 · 37 citations · Full text

Carnitine‐acylcarnitine translocase deficiency ‐ a mild phenotype

S. E. Olpin, James R. Bonham, M. Downing et al. · Journal of Inherited Metabolic Disease · 1997 · 37 citations

Carnitine‐acylcarnitine Translocase Deficiency, Translational Medicine, Genetic Disorder

The allopurinol load test lacks specificity for primary urea cycle defects but may indicate unrecognized mitochondrial disease

James R. Bonham, Philip A. I. Guthrie, M. Downing et al. · Journal of Inherited Metabolic Disease · 1999 · 32 citations