T. Richardson

n‐3 polyunsaturated fatty acid supplementation, monocyte adhesion molecule expression and pro‐inflammatory mediators in Type 2 diabetes mellitus

M. Sampson, D. Hughes, A. Sampson, 2001, Diabetic medicine : a journal of the British Diabetic Association.

Increased DNA oxidative susceptibility without increased plasma LDL oxidizability in Type II diabetes: effects of alpha-tocopherol supplementation.

M. Sampson, S. Astley, D. Hughes, 2001, Clinical science.

Cinacalcet for Symptomatic Hypercalcemia Caused by AP2S1 Mutations.

M. Nesbit, R. Thakker, F. Hannan, 2016, The New England journal of medicine.

Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype–phenotype correlations, codon bias and dominant-negative effects

J. Connell, S. Pearce, M. Porteous, 2015, Human molecular genetics.

A Follow-Up Study of the Prevalence of Valvular Heart Abnormalities in Hyperprolactinemic Patients Treated With Cabergoline.

R. Murray, W. Drake, N. Martin, 2016, The Journal of clinical endocrinology and metabolism.

Significant Benefits of AIP Testing and Clinical Screening in Familial Isolated and Young-onset Pituitary Tumors

Julian R. E. Davis, H. Randeva, R. Eeles, 2020, The Journal of clinical endocrinology and metabolism.

Multiple Endocrine Neoplasia Type 1 (MEN1) 5′UTR Deletion, in MEN1 Family, Decreases Menin Expression

A. Pagnamenta, Jenny C. Taylor, R. Thakker, 2020, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.