Showing 1 - 18 results of 18 for search 'Brain C', query time: 0.04s
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Exploration of Treatment-Resistant Schizophrenia Subtypes Based on a Survey of 204 US Psychiatrists by Correll CU, Brevig T, Brain C
Published 2019-12-01
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Nonadherence with antipsychotic medication in schizophrenia: challenges and management strategies by Haddad PM, Brain C, Scott J
Published 2014-06-01
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The pituitary gland is capable of responding to two successive doses of growth hormone releasing hormone (GHRH) by Suri, D, Hindmarsh, P, Matthews, DR, Brain, C, Brook, C
Published 1991Journal article -
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CALCULATION OF PITUITARY GROWTH-HORMONE (GH) SECRETION RATE IN CHILDREN by Hindmarsh, P, Matthews, D, Brain, C, Pringle, P, Brook, C
Published 1988Journal article -
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The interaction of growth hormone releasing hormone and somatostatin in the generation of a GH pulse in man. by Hindmarsh, P, Brain, C, Robinson, I, Matthews, DR, Brook, C
Published 1991Journal article -
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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
Published 2010Journal article -
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The half-life of exogenous growth hormone after suppression of endogenous growth hormone secretion with somatostatin. by Hindmarsh, P, Matthews, DR, Brain, C, Pringle, P, di Silvio, L, Kurtz, AB, Brook, C
Published 1989Journal article -
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Efficient short-term control of hypercortisolaemia by low-dose etomidate in severe paediatric Cushing's disease. by Greening, J, Brain, C, Perry, L, Mushtaq, I, Sales Marques, J, Grossman, AB, Savage, M
Published 2005Journal article -
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Stigma, discrimination and medication adherence in schizophrenia: Results from the Swedish COAST study by Brain, C, Sameby, B, Allerby, K, Quinlan, P, Joas, E, Lindström, E, Burns, T, Waern, M
Published 2014Journal article -
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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
Published 2010Journal article -
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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
Published 2014Journal article -
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Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites. by Hannan, F, Nesbit, M, Zhang, C, Cranston, T, Curley, A, Harding, B, Fratter, C, Rust, N, Christie, P, Turner, J, Lemos, M, Bowl, MR, Bouillon, R, Brain, C, Bridges, N, Burren, C, Connell, J, Jung, H, Marks, E, McCredie, D, Mughal, Z, Rodda, C, Tollefsen, S, Brown, E, Yang, J
Published 2012Journal article