Immune response of healthy adults to the ingested probiotic Lactobacillus casei Shirota by Harbige, Laurence S., Pinto, E., Allgrove, J., Thomas, L. V.

A missense glial cells missing homolog B (GCMB) mutation, Asn502His, causes autosomal dominant hypoparathyroidism. by Mirczuk, S, Bowl, MR, Nesbit, M, Cranston, T, Fratter, C, Allgrove, J, Brain, C, Thakker, R

Factors influencing skeletal maturation at diagnosis of paediatric Cushing's disease. by Peters, C, Ahmed, M, Storr, H, Davies, K, Martin, L, Allgrove, J, Grossman, AB, Savage, M

Factors influencing skeletal maturation at diagnosis of paediatric Cushing's disease by Peters, C, Ahmed, M, Storr, H, Davies, K, Martin, L, Grossman, AB, Allgrove, J, Savage, M

Use of Intravenous Etomidate in a Child To Control Acute Psychosis Induced by the Hypercortisolemia Secondary to Severe Cushing's Disease. by Chan, L, Hughes, C, Allgrove, J, Martin, L, Afshar, F, Hindmarsh, P, Savage, M, Grossman, AB, Storr, H

Use of intravenous etomidate to control acute psychosis induced by the hypercortisolaemia in severe paediatric Cushing's disease by Chan, L, Vaidya, M, Westphal, B, Allgrove, J, Martin, L, Afshar, F, Hindmarsh, P, Savage, M, Grossman, AB, Storr, H

Use of intravenous etomidate to control acute psychosis induced by the hypercortisolaemia in severe paediatric Cushing's disease. by Chan, L, Vaidya, M, Westphal, B, Allgrove, J, Martin, L, Afshar, F, Hindmarsh, P, Savage, M, Grossman, AB, Storr, H

PTH infusion for seizures in autosomal dominant hypocalcemia type 1 by Sastre, A, Valentino, K, Hannan, FM, Lines, KE, Gluck, AK, Stevenson, M, Ryalls, M, Gorrigan, RJ, Pullen, D, Buck, J, Sankaranarayanan, S, Allgrove, J, Thakker, RV, Gevers, EF

Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hyp... by Bowl, MR, Mirczuk, S, Grigorieva, I, Piret, SE, Cranston, T, Southam, L, Allgrove, J, Bahl, S, Brain, C, Loughlin, J, Mughal, Z, Ryan, F, Shaw, N, Thakker, Y, Tiosano, D, Nesbit, M, Thakker, R

Mutational analysis of the adaptor protein 2 sigma subunit (AP2S1) gene: search for autosomal dominant hypocalcemia type 3 (ADH3). by Rogers, A, Nesbit, M, Hannan, F, Howles, S, Gorvin, C, Cranston, T, Allgrove, J, Bevan, J, Bano, G, Brain, C, Datta, V, Grossman, A, Hodgson, S, Izatt, L, Millar-Jones, L, Pearce, S, Robertson, L, Selby, P, Shine, B, Snape, K, Warner, J, Thakker, R