Browsing by Author Storey, Elsdon

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Issue DateTitleAuthor(s)Citation
2012Aspirin for the prevention of cognitive decline in the elderly: rationale and design of a neuro-vascular imaging study (ENVIS-ion)Wang, Jie Jin; Abhayaratna, Walter; Budge, Marc; Essex, Rowan; Janke, Andrew; Kam, Anthony; Reid, Christopher; Storey, Elsdon; Tonkin, Andrew; Wong, Tien; Woods, Robyn; Western Clinical School: Westmead Millennium InstituteAspirin for the prevention of cognitive decline in the elderly: rationale and design of a neuro-vascular imaging study (ENVIS-ion), BMC Neurology, vol.12, N/A, 2012,pp 1-9
2014CANVAS an update: Clinical presentation, investigation and managementMacDougall, Hamish; Halmagyi, G; McLean, Catriona; Roberts, Leslie; Storey, Elsdon; Szmulewicz, David; PsychologyCANVAS an update: Clinical presentation, investigation and management, Journal of Vestibular Research: Equilibrium and Orientation, vol.24, 5-6, 2014,pp 465-474
2011Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): a review of the clinical features and video oculographic diagnosisMacDougall, Hamish; Chancellor, Andrew; Halmagyi, Michael; McLean, Catriona; Merchant, Saumil; Mossman, Stuart; Patrikios, Peter; Storey, Elsdon; Szmulewicz, David; Waterston, John; PsychologyCerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): a review of the clinical features and video oculographic diagnosis, Annals of the New York Academy of Sciences, vol.1233, N/A, 2011,pp 139-147
2009Development of a multiplex ligation-dependent probe amplification assay for diagnosis and estimation of the frequency of spinocerebellar ataxia type 15Nicholson, Garth; Wei, Morgan; Zhu, Danqing; Bruno, Damien; Delatycki, Martin; Ganesamoorthy, Devika; Gardner, R. J. McKinlay; Schoumans, Jacqueline; Slater, Howard; Storey, Elsdon; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: MedicineDevelopment of a multiplex ligation-dependent probe amplification assay for diagnosis and estimation of the frequency of spinocerebellar ataxia type 15, Clinical Chemistry (Washington, DC): international journal of molecular diagnostics and laboratory medicine, vol.55, 7,pp 1415-1418
2009Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathyKennerson, Marina; Nicholson, Garth; Baets, Jonathan; Berciano, Jose; Berneman, Zwi N.; Bienfait, Henriette; Claeys, Kristl; De Jonghe, Peter; De Veuster, Ilse; De Vriendt, Els; Garcia, Antonio; Lammens, Martin; Merory, John; Nelis, Eva; Storey, Elsdon; Timmerman, Vincent; Vance, Jefferey M.; Verhoeven, Kristien; Zuchner, Stephan; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research InstitutePhenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy, Brain, vol.132, 7, 2009,pp 1741-1752
2016Proposed diagnostic criteria for cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS)MacDougall, Hamish; Halmagyi, G. Michael; McLean, Catriona; Roberts, Leslie; Storey, Elsdon; Szmulewicz, David; PsychologyProposed diagnostic criteria for cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS), Neurology: Clinical Practice, vol.6, 1, 2016,pp 61-68
2003Spinocerebellar ataxia type 15 (SCA15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxix mouse mutantKennerson, Marina; Nicholson, Garth; Anney, Richard J; Forrest, Susan M; Knight, Melanie A; Matsuura, Tomokazu; McKinlay Garnder, R J; Salimi-Tari, Peyman; Storey, Elsdon; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research InstituteSpinocerebellar ataxia type 15 (SCA15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxix mouse mutant, Neurobiology of Disease, vol.13,(2),2003,pp 147-157