A. Briddon

Assessment of mitochondrial electron transport chain function in a primary astrocyte cell model of hyperhomocystinaemia

E. Murphy, I. Hargreaves, J. Land, 2013, Toxicology mechanisms and methods.

Homocysteine and cysteine – albumin binding in homocystinuria: assessment of cysteine status and implications for glutathione synthesis?

P. Lee, A. Briddon, I. Hargreaves, 2002, Amino Acids.

Blood mononuclear cell coenzyme Q10 concentration and mitochondrial respiratory chain succinate cytochrome-c reductase activity in phenylketonuric patients

J. Land, S. Heales, P. Lee, 2003, Journal of Inherited Metabolic Disease.

A rationale for cystine supplementation in severe homocystinuria

P. Lee, A. Briddon, 2007, Journal of Inherited Metabolic Disease.

Late onset heterozygous ornithine transcarbamylase deficiency mimicking complex partial status epilepticus

J. Duncan, J. Land, A. Briddon, 2000, Journal of neurology, neurosurgery, and psychiatry.

Impairment of the nitric oxide/cyclic GMP pathway in cerebellar slices prepared from thehph-1 mouse

S. Heales, J. Clark, J. Land, 1996, Brain Research.

Primary pyruvate dehydrogenase E3 binding protein deficiency with mild hyperlactataemia and hyperalaninaemia

M. Hanna, J. Land, S. Heales, 2003, Journal of Inherited Metabolic Disease.