Browsing by Author Richardson, Anne-Louise

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Issue DateTitleAuthor(s)Citation
2005Experience of prophylactic thyroidectomy in multiple endocrine neoplasia type 2A kindreds with RET codon 804 mutations.Delbridge, Leigh; Learoyd, Diana; Richardson, Anne-Louise; Robinson, Bruce; Conaglen, John V.; Elston, Marianne; Gosnell, Jessica; Saurine, Tricia J; Northern Clinical School: Surgery; Northern Clinical School: Medicine; Northern Clinical School: Molecular Medicine (Kolling I); Northern Clinical School: MedicineExperience of prophylactic thyroidectomy in multiple endocrine neoplasia type 2A kindreds with RET codon 804 mutations., Clinical Endocrinology, vol.63,(6),2005,pp 636-641
2003Genome-wide copy number imbalances identified in familial and sproadic medullary thyroid carcinomaDelbridge, Leigh; Marsh, Deborah; Philips, Jeanette; Richardson, Anne-Louise; Robinson, Bruce; Theodosopoulos, G; Martin-Schulte, Klaus; Roher, Hans-Dietrich; Northern Clinical School: Surgery; Northern Clinical School: Molecular Medicine (Kolling I); Medicine; Northern Clinical School: Molecular Medicine (Kolling I); Northern Clinical School: Medicine; Molecular & Microbial BioscienGenome-wide copy number imbalances identified in familial and sproadic medullary thyroid carcinoma, Journal of Clinical Endocrinology and Metabolism, vol.88,(4),2003,pp 1866-1872
2004Germline And De Novo Mutations In The Hrpt2 Tumour Suppressor Gene In Familial Isolated Hyperparathyroidism (Fihp).Delbridge, Leigh; Richardson, Anne-Louise; Robinson, Bruce; Bauters, C; Calender, A; Carpten, J D; Cheng, J D; Ebeling, T; Forsberg, L; Hoog, A; Kahnoski, K; Larsson, C; Meyrier, A; Petillo, D; Proye, C; Salmela, P I; Teh, B T; Villablanca, A; Northern Clinical School: Surgery; Northern Clinical School: Molecular Medicine (Kolling I); Northern Clinical School: MedicineGermline And De Novo Mutations In The Hrpt2 Tumour Suppressor Gene In Familial Isolated Hyperparathyroidism (Fihp)., Journal of Medical Genetics 2005, vol.41,(3),2004,pp e32 - 1-e32 - 7
2003Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporatid phaeochromaocytomasBambach, Chris; Benn, Diana; Delbridge, Leigh; Marsh, Deborah; Richardson, Anne-Louise; Robinson, Bruce; Croxson, Michael S.; Hammond, Jeremy; Pullan, Peter T; Tucker, Kathy; Northern Clinical School: Surgery; Northern Clinical School: Molecular Medicine (Kolling I); Northern Clinical School: Surgery; Northern Clinical School: Molecular Medicine (Kolling I); Northern Clinical School: Molecular Medicine (Kolling I); Northern Clinical School: MedicineNovel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporatid phaeochromaocytomas, Oncogene: including Oncogene Reviews, vol.22,(9),2003,pp 1358-1364
2006Rapid Mutation Screening for HRPT2 and MEN1 Mutations Associated with Familial and Sporadic Primary Hyperparathyroidism.Howell, Viive; Marsh, Deborah; Richardson, Anne-Louise; Robinson, Bruce; Cardinal, John W.; Gimm, Oliver; Northern Clinical School: Molecular Medicine (Kolling I); Northern Clinical School: Molecular Medicine (Kolling I); Northern Clinical School: Molecular Medicine (Kolling I); Northern Clinical School: MedicineRapid Mutation Screening for HRPT2 and MEN1 Mutations Associated with Familial and Sporadic Primary Hyperparathyroidism., Journal of molecular diagnostics, vol.8,(5),2006,pp 559-566