A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism

por Koulouri, O., Nicholas, A. K., Schoenmakers, E., Mokrosinski, J., Lane, F., Cole, T., Kirk, J., Farooqi, I. S., Chatterjee, V. K., Gurnell, M., Schoenmakers, N.
Publicado 2016

An approach to quantifying abnormalities in energy expenditure and lean mass in metabolic disease

por Watson, L P E, Raymond-Barker, P, Moran, C, Schoenmakers, N, Mitchell, C, Bluck, L, Chatterjee, V K, Savage, D B, Murgatroyd, P R
Publicado 2014

Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and Ireland

por Nicholas, A.K., Jaleel, S., Lyons, G., Schoenmakers, E., Dattani, M.T., Crowne, E., Bernhard, B., Kirk, J., Roche, E.F., Chatterjee, V.K., Schoenmakers, N.
Publicado 2016

Mild cold effects on hunger, food intake, satiety and skin temperature in humans

por Langeveld, M, Tan, C Y, Soeters, M R, Virtue, S, Ambler, G K, Watson, L P E, Murgatroyd, P R, Chatterjee, V K, Vidal-Puig, A
Publicado 2016

Rapid disease progression in a patient with mismatch repair-deficient and cortisol secreting adrenocortical carcinoma treated with pembrolizumab

por Casey, R.T., Giger, O., Seetho, I., Marker, A., Pitfield, D., Boyle, L.H., Gurnell, M., Shaw, A., Tischkowitz, M., Maher, E.R., Chatterjee, V.K., Janowitz, T., Mells, G., Corrie, P., Challis, B.G.
Publicado 2018