D. Stansbie

Y. Wilson, C. Irvine, R. Baird, 1996, European journal of vascular and endovascular surgery : the official journal of the European Society for Vascular Surgery.

CREATINE KINASE MB IN MARATHON RUNNERS

D. Stansbie, J. P. Aston, N. Powell, 1982, The Lancet.

Effect of exercise on plasma pyruvate kinase and creatine kinase activity.

N. Dallimore, H. Williams, D. Stansbie, 1983, Clinica chimica acta; international journal of clinical chemistry.

Neonatal Parenteral Nutrition with a Fat Emulsion Containing Medium Chain Triglycerides

O. P. Gray, P. Rowlandson, D. Stansbie, 1988, Acta paediatrica Scandinavica.

Stabilization of Blood Homocysteine by 3-Deazaadenosine

A. Bowron, D. Stansbie, A. Day, 1998, Annals of clinical biochemistry.

Regulation of pyruvate dehydrogenase and pyruvate dehydrogenase phosphate phosphatase activity in rat epididymal fat-pads. Effects of starvation, alloxan-diabetes and high-fat diet.

R. Denton, P. J. Randle, D. Stansbie, 1976, The Biochemical journal.

Acute effects in vivo of anti-insulin serum on rates of fatty acid synthesis and activities of acetyl-coenzyme A carboxylase and pyruvate dehydrogenase in liver and epididymal adipose tissue of fed rats.

R. Denton, R. Brownsey, D. Stansbie, 1976, The Biochemical journal.

Mitochondrial myopathy with skeletal muscle cytochrome oxidase deficiency

D. Turnbull, M. Johnson, A. Cross, 1982, Journal of Inherited Metabolic Disease.

Fatal infantile mitochondrial myopathy due to cytochrome c oxidase deficiency

D. Turnbull, M. Johnson, I. Hughes, 1983, Journal of the Neurological Sciences.

Disorders of the pyruvate dehydrogenase complex

C. Marsac, D. Stansbie, S. Wallace, 1986, Journal of Inherited Metabolic Disease.

Regulation of the conversion of glucose into fat in white adipose tissue by insulin [proceedings].

R. Denton, R. Brownsey, D. Stansbie, 1977, Biochemical Society transactions.

Glycosaminoglycan Fractions in Normal Human Urine

D. Stansbie, C. Pennock, R. Charles, 1975, Annals of clinical biochemistry.

Blood spot homocysteine: a feasibility and stability study.

A. Bowron, D. Stansbie, Jeff Scott, 2005, Clinical chemistry.

Assessment of homocysteine as a cardiovascular risk factor in clinical practice

R. Clarke, D. Stansbie, 2001, Annals of clinical biochemistry.

Addition of 3-deazaadenosine to vacutainer tubes stabilizes whole-blood homocysteine for at least 6 hours at ambient temperature.

A. Bowron, D. Stansbie, 2003, Clinical chemistry.

C677T (thermolabile alanine/valine) polymorphism in methylenetetrahydrofolate reductase (MTHFR): its frequency and impact on plasma homocysteine concentration in different European populations. EARS group.

V. Gudnason, S. Humphries, V. Nicaud, 1997, Atherosclerosis.

Abbott Imx Homocysteine Assay: Significant Interference by 3-Deazaadenosine

A. Bowron, W. Woltersdorf, D. Stansbie, 1999, Annals of clinical biochemistry.

Gene-environment and Gene-gene Interaction in the Determination of Plasma Homocysteine Levels in Healthy Middle-aged Men

V. Gudnason, E. Hawe, G. Miller, 2001, Thrombosis and Haemostasis.

Cost-Effective Strategy for the Serological Investigation of Coeliac Disease

M. Moorghen, Janet Stone, A. Bowron, 2000, Annals of clinical biochemistry.

Linkage disequilibrium at the cystathionine beta synthase (CBS) locus and the association between genetic variation at the CBS locus and plasma levels of homocysteine. The Ears II Group. European Atherosclerosis Research Study.

V. Gudnason, S. Humphries, V. Nicaud, 1998, Annals of human genetics.

The association of birthweight and contemporary size with insulin resistance among children from Estonia and Denmark: findings from the European Youth Heart Study

D. Lawlor, K. Froberg, A. Page, 2005, Diabetic medicine : a journal of the British Diabetic Association.

A coupled fluorometric rate assay for pyruvate dehydrogenase in cultured human fibroblasts.

D. Stansbie, M. Solomon, 1984, Analytical biochemistry.

Fructose load test—anin vivo screening test designed to assess pyruvate dehydrogenase activity and interconversion

R. Denton, D. Stansbie, R. J. Sherriff, 1978, Journal of Inherited Metabolic Disease.

Homocysteine: An independent risk factor for the failure of vascular intervention

Y. Wilson, W. Tennant, R. Baird, 1996, The British journal of surgery.

Infant feeding and components of the metabolic syndrome: findings from the European Youth Heart Study

George Davey Smith, D. Lawlor, L. Andersen, 2005, Archives of Disease in Childhood.

Defect in the lipoyl-bearing protein X subunit of the pyruvate dehydrogenase complex in two patients with encephalomyelopathy.

P. Jehenson, G. Bonne, C. Marsac, 1993, The Journal of pediatrics.

The influence of genetic and environmental factors on plasma homocysteine concentrations in a population at high risk for coronary artery disease

A. Bowron, D. Stansbie, Jeff Scott, 2005, Annals of clinical biochemistry.

Postmortem diagnosis of familial hypercholesterolaemia.

D. Stansbie, S. Leadbeatter, 1984, British medical journal.

Linkage disequilibrium at the cystathionine β synthase (CBS) locus and the association between genetic variation at the CBS locus and plasma levels of homocysteine

V. Gudnason, S. Humphries, V. Nicaud, 1998 .

Biochemical diagnosis ofmyocardial infarction? Cardiac enzymes orcaveat emptor

D. Stansbie, 1994 .

Familial pseudohyperkalaemia: inhibition of erythrocyte K+ efflux at 4 degrees C by quinine.

D. Stansbie, D. James, 1987, Clinical science.

Plasma puryvate kinase and creatine kinase activity in Becker muscular dystrophy

H. Kingston, I. Ramasamy, D. Stansbie, 1984, Journal of the Neurological Sciences.

Regulation of the human pyruvate dehydrogenase complex.

D. Stansbie, 1976, Clinical science and molecular medicine.