Prof Elsdon Storey - Researcher Profile

Biography

Elsdon works in the Faculty of Medicine, Nursing & Health Sciences at Monash University as a Professor.

Related Links:

• Elsdon is Director of the Van Cleef/Roet Centre for Nervous Diseases, at the Alfred Medical Research and Education Precinct. See detail at: http://www.med.monash.edu.au//medicine/alfred/research/neuroscience/index.html

Qualifications

PHILOSOPHY

Institution: Oxford University

Year awarded: 1986

MEDICINE , SURGERY

Institution: University of Melbourne

Year awarded: 1978

Publications

Book Chapters

Storey, E., Mckinlay Gardner, R., 2012, Spinocerebellar ataxia type 15, in Handbook of Clinical Neurology, eds Michael J. Aminoff, Francois Boller, Dick F. Swaab, Elsevier, The Netherlands, pp. 561-565.

Storey, E., Mckinlay Gardner, R., 2012, Spinocerebellar ataxia type 20, in Handbook of Clinical Neurology, eds Michael J. Aminoff, Francois Boller, Dick F. Swaab, Elsevier, The Netherlands, pp. 567-573.

Kinsella, G.J., Storey, E., Crawford, J.R., 2007, Executive function and its assessment, in Neurology and Clinical Neuroscience, eds Anthony H.V. Schapira, Mosby, USA, pp. 83-95.

Kazemi, N.J., Kaye, A.H., Storey, E., 2007, Hydrocephalus including normal-pressure hydrocephalus, in Neurology and Clinical Neuroscience, eds Anthony H.V. Schapira, Mosby, USA, pp. 825-833.

Storey, E., Kinsella, G.J., 2007, Principles of neuropsychometric assessment, in Neurology and Clinical Neuroscience, eds Anthony H.V. Schapira, Mosby, USA, pp. 22-30.

Storey, E., 2007, The neglect syndrome, in Neurology and Clinical Neuroscience, eds Anthony H.V. Schapira, Mosby, USA, pp. 73-82.

Kelly, L., Storey, E., 2007, The ubiquitin-proteasome system in Huntington's disease and other polyglutamine diseases, in The Ubiquitin Proteasome System in the Central Nervous System: From Physiology to Pathology, eds Mario Di Napoli, Cezary Wojcik, Nova Science Publishers, United States, pp. 793-812.

Storey, E., 2005, The cerebellum and cognitive impairment, in Dementia, eds Alistair Burns, John O'Brien, David Ames, Hodder Arnold, London UK, pp. 713-719.

Journal Articles

Nag, N., Tarlac, V., Storey, E., 2013, Assessing the efficacy of specific cerebellomodulatory drugs for use as therapy for spinocerebellar ataxia type 1, Cerebellum [P], vol 12, issue 1, Springer New York LLC, United States, pp. 74-82.

Akhlaghi, H., Corben, L.A., Georgiou-Karistianis, N., Bradshaw, J.L., Delatycki, M., Storey, E., Egan, G.F., 2012, A functional MRI study of motor dysfunction in Friedreich's ataxia, Brain Research [P], vol 1471, Elsevier, Netherlands, pp. 138-154.

Reid, C.M., Storey, E., Wong, T.Y., Woods, R.L., Tonkin, A.M., Wang, J.J., Kam, A., Janke, A., Essex, R., Abhayaratna, W., Budge, M., 2012, Aspirin for the prevention of cognitive decline in the elderly: rationale and design of a neuro-vascular imaging study (ENVIS-ion), BMC Neurology [P], vol 12, issue 3, BioMed Central Ltd, UK, pp. 1-9.

Reid, C., Storey, E., Wong, T., Woods, R., Tonkin, A., Wang, J., KAM, A., Janke, A., Essex, R., Abhayaratna, W., Budge, M., 2012, Aspiring for the prevention of cognitive decline in the elderly: rationale and design of a neuro-vascular imaging study (ENVIS-ion), BMC Neurology [P], vol 12, issue 3, Biomed Central Ltd, England, pp. 1-9.

Chaudhuri, K., Storey, E., Lee, G.A., Bailey, M.J., Chan, J.C.Y., Rosenfeldt, F.L., Pick, A., Negri, J., Gooi, J., Zimmet, A., Esmore, D.S., Merry, C., Rowland, M., Lin, E., Marasco, S., 2012, Carbon dioxide insufflation in open-chamber cardiac surgery: A double-blind, randomized clinical trial of neurocognitive effects, Journal of Thoracic and Cardiovascular Surgery [P], vol 144, Mosby, Inc, USA, pp. 646-653.

Delprado, J., Kinsella, G., Ong, B., Pike, K., Ames, D., Storey, E., Saling, M., Clare, L., Mullaly, E., Rand, E., 2012, Clinical measures of prospective memory in amnestic mild cognitive impairment , Journal of the International Neuropsychological Society : JINS [E], vol 18, issue 2, Cambridge University Press, United Kingdom, pp. 295-304.

Lee, W., Williams, D., Storey, E., 2012, Cognitive testing in the diagnosis of parkinsonian disorders: a critical appraisal of the literature, Movement Disorders [P], vol 27, issue 10, ohn Wiley & Sons Inc., United States, pp. 1243-1254.

Georgiou-Karistianis, N., Akhlaghi, H., Corben, L.A., Delatycki, M., Storey, E., Bradshaw, J.L., Egan, G.F., 2012, Decreased functional brain activation in Friedreich ataxia using the Simon effect task, Brain And Cognition [P], vol 79, issue 3, Academic Press, United States, pp. 200-208.

Godler, D., Slater, H., Bui, Q., Storey, E., Ono, M., Gehling, F., Inaba, Y., Francis, D., Hopper, J., Kinsella, G., Amor, D., Hagerman, R., Loesch, D., 2012, Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot study, Clinical Chemistry [P], vol 58, issue 3, American Association for Clinical Chemistry, Inc., United States, pp. 590-598.

Tarlac, V., Kelly, L., Nag, N., Allen-Graham, J., Anderson, R.P., Storey, E., 2012, HLA-DR3-DQ2 mice do not develop ataxia in the presence of high titre anti-gliadin antibodies, Cerebellum [E], vol 3.207, Springer, New York, USA.

Pike, K., Kinsella, G., Ong, B., Mullaly, E., Rand, E., Storey, E., Ames, D., Saling, M., Clare, L., Parsons, S., 2012, Names and numberplates: quasi-everyday associative memory tasks for distinguishing amnestic mild cognitive impairment from healthy aging, Journal Of Clinical And Experimental Neuropsychology [P], vol 34, issue 3, Psychology Press, United Kingdom, pp. 269-278.

Szmulewicz, D., Waterston, J., MacDougall, H., Mossman, S., Chancellor, A., McLean, C., Merchant, S., Patrikios, P., Halmagyi, M., Storey, E., 2011, Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): a review of the clinical features and video-oculographic diagnosis, Annals of the New York Academy of Sciences [P], vol 1233, Wiley-Blackwell Publishing, Inc, United States, pp. 139-147.

Loesch, D., Godler, D., Evans, A., Bui, Q., Gehling, F., Kotschet, K., Trost, N., Storey, E., Stimpson, P., Kinsella, G., Francis, D., Thorburn, D., Venn, A., Slater, H., Horne, M., 2011, Evidence for the toxicity of bidirectional transcripts and mitochondrial dysfunction in blood associated with small CGG expansions in the FMR1 gene in patients with parkinsonism, Genetics In Medicine [P], vol 13, issue 5, Nature Publishing Group, USA, pp. 392-399.

Corben, L., Akhlaghi, H., Georgiou-Karistianis, N., Bradshaw, J., Egan, G., Storey, E., Churchyard, A., Delatycki, M., 2011, Impaired inhibition of prepotent motor tendencies in Friedreich ataxia demonstrated by the Simon interference task, Brain And Cognition [P], vol 76, issue 1, Academic Press, United States, pp. 140-145.

Hutchens, R., Kinsella, G., Ong, B., Pike, K., Parsons, S., Storey, E., Ames, D., Saling, M., Mullaly, E., Rand, E., Clare, L., 2011, Knowledge and use of memory strategies in amnestic mild cognitive impairment, Psychology and Aging [P], vol E, American Psychological Association, United States, pp. 1-10.

Szmulewicz, D., Waterston, J., Halmagyi, G.M., Mossman, S., Chancellor, A., McLean, C., Storey, E., 2011, Sensory neuropathy as part of the cerebellar ataxia neuropathy vestibular areflexia syndrome, Neurology [P], vol 76, Lippincott Williams & Wilkins, USA, pp. 1903-1910.

O'Halloran, C., Kinsella, G., Storey, E., 2011, The cerebellum and neuropsychological functioning: A critical review, Journal Of Clinical And Experimental Neuropsychology [P], vol 34, issue 1, Psychology Press, United Kingdom, pp. 35-56.

Szmulewicz, D., Storey, E., 2010, Bilateral dentate nucleus hyperintensities, Journal of Clinical Neuroscience [P], vol 17, issue 11, Churchill Livingstone Elsevier, United Kingdom, p. 1406.

Husain-Ponnampalam, R., Turnbull, V., Tarlac, V., Storey, E., 2010, Expression and purification of ataxin-1 protein, Journal of Neuroscience Methods [P], vol 189, issue 1, Elsevier BV, Netherlands, pp. 30-35.

Price, S.E., Kinsella, G.J., Ong, B., Mullaly, E., Phillips, M., Pangnadasa-Fox, L., Perre, D., Storey, E., 2010, Learning and memory in amnestic mild cognitive impairment: Contribution of working memory, Journal Of The International Neuropsychological Soci..., vol 16, issue 2, Cambridge University Press, UK, USA, pp. 342-351.

Markman, P.L., Rowland, M., Leong, J., Van Der Merwe, J., Storey, E., Marasco, S., Negri, J., Bailey, M.J., Rosenfeldt, F.L., 2010, Skeletonized internal thoracic artery harvesting reduces chest wall dysesthesia after coronary bypass surgery, Journal of Thoracic and Cardiovascular Surgery [P], vol 139, issue 3, Mosby, Inc., United States, pp. 674-679.

Akhlaghi, H., Corben, L., Georgiou-Karistianis, N., Bradshaw, J., Storey, E., Delatycki, M., Egan, G., 2010, Superior cerebellar peduncle atrophy in Friedreich's ataxia correlates with disease symptoms, Cerebellum [P], vol 10, issue 1, Springer, USA, pp. 81-87.

Storey, E., Bahlo, M., Fahey, M.C., Sisson, O., Lueck, C.J., Gardner, R.J.M., 2009, A new dominantly inherited pure cerebellar ataxia, SCA 30, Journal of Neurology, Neurosurgery and Psychiatry, vol 80, issue 4, BMJ Group, UK, pp. 408-411.

Ganesamoorthy, D., Bruno, D.L., Schoumans, J., Storey, E., Delatycki, M.B., Zhu, D., Wei, M., Nicholson, G.A., McKinley Gardner, R.J., Slater, H., 2009, Development of a multiplex ligation-dependent probe amplification assay for diagnosis and estimation of the frequency of spinocerebellar ataxia type 15, Clinical Chemistry [P], vol 55, issue 7, American Association for Clinical Chemistry, Inc, United States, pp. 1415-1418.

Kinsella, G.J., Mullaly, E., Rand, E., Ong, B., Burton, C., Price, S.E., Phillips, M., Storey, E., 2009, Early intervention for mild cognitive impairment: A randomised controlled trial, Journal Of Neurology Neurosurgery And Psychiatry [P], vol 80, issue 7, BMJ Group, United Kingdom, pp. 730-736.

Chang, C.C., McLean, C., Vujovic, O., Jenney, A.J., Short, M., Lyon, S., Storey, E., Lewin, S.R., 2009, Fatal acute varicella-zoster virus hemorrhagic meningomyelitis with necrotizing vasculitis in an HIV-infected patient, Clinical Infectious Diseases [P], vol 48, issue 1, University of Chicago Press, United States, pp. 372-373.

Claeys, K.G., Zuchner, S., Kennerson, M.L., Berciano, J., Garcia, A., Verhoeven, K., Storey, E., Merory, J.R., Bienfait, H.M., Lammens, M., Nelis, E., Baets, J., De Vriendt, E., Berneman, Z.N., De Veuster, I., Vance, J.M., Nicholson, G.A., Timmerman, V., De Jonghe, P., 2009, Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy, Brain [P], vol 132, issue 7, Oxford University Press, United Kingdom, pp. 1741-1752.

Knight, M., Hernandez, D., Diede, S.J., Dauwerse, H.G., Rafferty, I., van de Leemput, J., Forrest, S.M., Gardner, R.J.M., Storey, E., van Ommen, G.B., Tapscott, S.J., Fischbeck, K.H., Singleton, A.B., 2008, A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20, Human Molecular Genetics, vol 17, issue 24, Oxford University Press, Oxford England, pp. 3847-3853.

Loesch, D.Z., Cook, M.J., Litewka, L., Gould, E., Churchyard, A.J., Tassone, F., Slater, H., Storey, E., 2008, A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes, Journal of Medical Genetics, vol 45, issue 3, BMJ Publishing Group, UK, pp. 179-181.

Nelson, M., Reid, C.M., Ames, D.A., Beilin, L.J., Donnan, G.A., Gibbs, P., Johnston, C.I., Krum, H., Storey, E., Tonkin, A.M., Wolfe, R.S.J., Woods, R.L., McNeil, J.J., 2008, Feasibility of conducting a primary prevention trial of low-dose aspirin for major adverse cardiovascular events in older people in Australia: Results from the ASPirin in Reducing Events in the Elderly (ASPREE) pilot study, Medical Journal of Australia, vol 189, issue 2, Australasian Medical Publishing Company Pty. Ltd., Australia, pp. 105-109.

Bermingham, N., Cowie, T.F., Paine, E., Storey, E., McLean, C., 2008, Frontotemporal dementia and Parkinsonism linked to chromosome 17 in a young Australian patient with the G389R Tau mutation, Neuropathology and Applied Neurobiology, vol 34 Epub, issue 3, Blackwell Scientific Publications, England, pp. 366-370.

Ramsden, C.M., Kinsella, G.J., Ong, B., Storey, E., 2008, Performance of everyday actions in mild Alzheimer's disease, Neuropsychology, vol 22, American Psychological Association, USA, pp. 17-26.

Webb, T.E., Poulter, M., Beck, J., Uphill, J., Adamson, G., Campbell, T., Linehan, J., Powell, C., Brandner, S., Pal, S., Siddique, D., Wadsworth, J.D., Joiner, S., Alner, K., Petersen, C., Hampson, S., Rhymes, C., Treacy, C., Storey, E., Geschwind, M.D., Nemeth, A.H., Wroe, S., Collinge, J., Mead, S., 2008, Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series, Brain, vol 131, issue 10, Oxford University Press, Oxford, England, pp. 2632-2646.

Germano, C., Kinsella, G.J., Storey, E., Ong, B., Ames, D.J., 2008, The episodic buffer and learning in early Alzheimer's disease, Journal of Clinical and Experimental Neuropsychology, vol 30, Psychology Press, UK, pp. 627-638.

van de Leemput, J., Chandran, J., Knight, M., Holtzclaw, L.A., Scholz, S., Cookson, M.R., Houlden, H., Gwinn-Hardy, K., Fung, H.C., Lin, X., Hernandez, D., Simon-Sanchez, J., Wood, N., Giunti, P., Rafferty, I., Hardy, J., Storey, E., Gardner, R., Forrest, S.M., Fisher, E.M., Russell, J.T., Cai, H., Singleton, A.B., 2007, Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans, Public Library of Science Genetics, vol 3, issue 6, Public Library of Science, USA, pp. 1076-1082.

Kinsella, G.J., Ong, B., Storey, E., Wallace, J., Hester, R., 2007, Elaborated spaced-retrieval and prospective memory in mild Alzheimer's disease, Neuropsychological Rehabilitation, vol 17, issue 6, Psychology Press, UK, pp. 688-706.

Tarlac, V., Turnbull, V.J., Stefani, D., Kelly, L., Walsh, R., Storey, E., 2007, Inclusion formation by ataxins -1, -2, -3, and -7, International Journal of Neuroscience, vol 117, issue 9, Taylor & Francis Ltd, UK, pp. 1289-1314.

Corben, L.A., Georgiou-Karistianis, N., Fahey, M.C., Storey, E., Churchyard, A.J., Horne, M., Bradshaw, J.L., Delatycki, M.B., 2006, Towards an understanding of cognitive function in Friedreich ataxia, Brain Research Bulletin, vol 70, issue 3, Elsevier, Kidlington England, pp. 197-202.

Storey, E., 2005, Ballistic tracking as all exploratory tool in cerebellar disease, Journal of The Neurological Sciences, vol 238, Elsevier Science BV, Amsterdam Netherlands, p. S201.

Vinton, A., Fahey, M.C., O'Brien, T.J., Shaw, J.H., Storey, E., Gardner, R.J.M., Mitchell, P.J., Du Sart, D., King, J.O., 2005, Dentatorubral-pallidoluysian atrophy in three generations, with clinical courses from nearly asymptomatic elderly to severe juvenile, in an Australian family of Macedonian descent, American Journal of Medical Genetics, vol 136 A, issue 2, John Wiley and Sons, Inc., USA, pp. 201-204.

Storey, E., Billimoria, P., 2005, Increased T2 signal in the middle cerebellar peduncles on MRI is not specific for fragile X p4remutation syndrome, Journal of Clinical Neuroscience, vol 12, issue 1, Churchill Livingstone, UK, pp. 42-43.

Fahey, M.C., Knight, M., Shaw, J.H., Gardner, R.J.M., Du Sart, D., Lockhart, P.J., Delatycki, M.B., Gates, P.C., Storey, E., 2005, Spinocerebellar ataxia type 14: Study of a family with an exon 5 mutation in the PRKCG gene, Journal of Neurology, Neurosurgery and Psychiatry, vol 76, issue 12, BMJ Publishing Group, UK, pp. 1720-1722.

Gardner, R.J.M., Knight, M.A., Hara, K., Tsuji, S., Forrest, S.M., Storey, E., 2005, Spinocerebellar ataxia type 15, The Cerebellum, vol 4, issue 1, Taylor & Francis Group Ltd, Abingdon England, pp. 47-50.

Storey, E., Knight, M., Forrest, S.M., Gardner, R.J.M., 2005, Spinocerebellar ataxia type 20, The Cerebellum, vol 4, issue 1, Taylor & Francis Ltd, UK, pp. 55-57.

Walsh, R., Storey, E., Stefani, D., Kelly, L., Turnbull, V.J., 2005, The roles of proteolysis and nuclear localisation in the toxicity of the polyglutamine diseases. A review, Neurotoxicity Research, vol 7, issue 1,2, FP Graham Publishing Company, USA, pp. 43-57.

Storey, E., 2005, Towards a functional topography of the cerebellum, Journal of The Neurological Sciences, vol 238, Elsevier Science BV, Amsterdam Netherlands, pp. S19-S20.

Elkadi, S., Krum, H., Storey, E., 2005, Vistio-spatial and verbal memory impairments in congestive heart failure patients, Journal of The Neurological Sciences, vol 238, Elsevier Science BV, Amsterdam Netherlands, p. S507.

van der Knaap, M.S., Leegwater, P.A.J., van Berkel, C.G.M., Brenner, C., Storey, E., Di Rocco, M., Salvi, F., Pronk, J.C., 2004, Arg113His mutation in eIF2B as cause of leukoencephalopathy in adults, Neurology, vol 62, issue 9, Lippincott Williams & Wilkins, USA, pp. 1598-1600.

Turnbull, V.J., Storey, E., Tarlac, V., Walsh, R., Stefani, D., Clark, R., Kelly, L., 2004, Different ataxin-2 antibodies display different immunoreactive profiles, Brain Research, vol 1027, issue 1-Feb, Elsevier Science BV, Netherland, pp. 103-116.

Knight, M., Gardner, R.J.M., Bahlo, M., Matsuura, T., Dixon, J.A., Forrest, S.M., Storey, E., 2004, Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20, Brain, vol 127, issue 5, Oxford University Press, UK, pp. 1172-1181.

Storey, E., Tuck, K., Hester, R., Hughes, A., Churchyard, A.J., 2004, Inter-rater reliability of the International Cooperative Ataxia Rating Scale (ICARS), Movement Disorders, vol 19, issue 2, Wiley-Liss, Hoboken, USA, pp. 190-192.

Storey, E., 2004, The frontal dementias, Neurology Asia, vol 9, Association of South East Asian Nations Neurological Association, Malaysia, pp. 11-20.

Aksoy, H., Dean, G., Elian, M., Deng, H.X., Deng, G., Juneja, T., Storey, E., McKinlay Gardner, R.J., Jacob, R.L., Laing, N.G., Siddique, T., 2003, A4T Mutation in the SOD1 gene causing familial amyotrophic lateral sclerosis, Neuroepidemiology, vol 22, issue 4, Karger, Basel Switzerland, pp. 235-238.

Nelson, M.R., Reid, C.M., Beilin, L.J., Donnan, G.A., Johnston, C.I., Krum, H., Storey, E., Tonkin, A.M., McNeil, J.J., 2003, Rationale for a trial of low-dose aspirin for the primary prevention of major adverse cardiovascular events and vascular dementia in the elderly, Drugs & Aging, vol 20, issue 12, Adis International Ltd, Auckland New Zealand, pp. 897-903.

Tarlac, V., Storey, E., 2003, Role of proteolysis in polyglutamine disorders, Journal of Neuroscience Research, vol 74, issue 3, John Wiley & Sons, Inc., New York USA, pp. 406-416.

Knight, M., Kennerson, M.L., Anney, R.J., Matsuura, T., Nicholson, G.A., Salimi-Tari, P., McKinlay Gardner, R.J., Storey, E., Forrest, S.M., 2003, Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant, Neurobiology of Disease, vol 13, issue 2, Academic Press Inc, Elsevier Science, San Diego USA, pp. 147-157.

Fuller, S.J., Storey, E., Li, Q., Beyreuther, K., Masters, C.L., 2002, Alzheimer's disease Apeptides are secreted by fresh and transformed human lymphocytes, Alzheimer's Reports, vol 5, issue 2, Medical Science Journals, Cambridge, pp. 29-40.

Slavin, M.J., Mattingley, J.B., Bradshaw, J.L., Storey, E., 2002, Local-global processing in Alzheimer's disease: an examination of interference, inhibition and priming, Neuropsychologia, vol 40, Pergamon Elsevier Science Ltd, Oxford UK, pp. 1173-1186.

Storey, E., Slavin, M.J., Kinsella, G.J., 2002, Patterns of cognitive impairment in Alzheimer's Disease: Assessment and differential diagnosis, Frontiers in Bioscience, vol 7, Frontiers in Bioscience Inc, New York NY USA, pp. e155-e184.

Storey, E., Gardner, R.J.M., Knight, M.A., Kennerson, M.L., Tuck, R.R., Forrest, S.M., Nicholson, G.A., 2001, A new autosomal dominant pure cerebellar ataxia, Neurology, vol 57, Lippincott Williams & Wilkins, Philadelphia USA, pp. 1913-1915.

Hand, P.J., Gardner, R.J.M., Knight, M., Forrest, S.M., Storey, E., 2001, Clinical features of a large Australian pedigree with episodic ataxia type 1. Editor-solicited videotape, Movement Disorders, vol 16, issue 5, Wiley-Liss, Hoboken, USA, pp. 938-939.

Kennerson, M.L., Zhu, D., Gardner, R.J.M., Storey, E., Merory, J., Robertson, S.P., Nicholson, G.A., 2001, Dominant intermediate Charcot-Marie-Tooth neuropathy maps to chromosome 19p12-p13.2, American Journal of Human Genetics, vol 69, University of Chicago Press, USA, pp. 883-888.

Poon, M.A., Stuckey, S., Storey, E., 2001, MRI evidence of cerebellar and hippocampal involvement in Creutzfeldt-Jakob disease, Neuroradiology, vol 43, Springer, New York, USA, pp. 746-749.

Gardner, R.J.M., Coleman, L.T., Mitchell, L.A., Smith, L.J., Harvey, A.S., Scheffer, I.E., Storey, E., Nowotny, M.J., Sloane, R.A., Lubitz, L., 2001, Near-total absence of the cerebellum, Neuropediatrics, vol 32, Georg Thieme Verlag KG, Germany, pp. 62-68.

Amor, D.J., Delatycki, M.B., Mckinley Gardner, R.J., Storey, E., 2001, New variant of familial cerebellar ataxia with hypergonadotropic hypogonadism and sensorineural deafness, American Journal of Medical Genetics, vol 99, Wiley-Liss, Inc, New Yok USA, pp. 29-33.

Brodaty, H., Ames, D.J., Boundy, K.L., Hecker, J., Snowden, J., Storey, E., Yates, M.W., 2001, Pharmacological treatment of cognitive deficits in Alzheimer's disease, Medical Journal of Australia, vol 175, Australasian Medicine Publishing Co Ltd, Pyrmont, NSW, Australia, pp. 324-329.

Storey, E., Du Sart, D., Shaw, J.H., Lorentzos, P., Kelly, L., McKinley Gardner, R.J., Forrest, S.M., Biros, I., Nicholson, G.A., 2000, Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia, American Journal of Medical Genetics, vol 95, Wiey-Liss, Division of John Wiley & Sons, New York NY USA, pp. 351-357.

Knight, M., Storey, E., Gardner, R.J.M., Hand, P.J., Forrest, S.M., 2000, Identification of a novel missense mutation L329I in the episodic ataxia type 1 gene KCNA1 - a challenging problem (Mutation and Polymorphism Report), Human Mutation, vol 16, issue 4, John Wiley & Sons, Inc, USA, pp. 374-376.

Storey, E., Katz, M., Brickman, Y., Beyreuther, K., Masters, C.L., 1999, Amyloid precursor protein of Alzheimer's disease: evidence for a stable, full-length, trans-membrane pool in primary neuronal cultures, European Journal of Neuroscience, vol 11, Blackwell Science Ltd, Oxford UK, pp. 1779-1788.

Delatycki, M.B., Damien, B.B., Gardner, R.J., Nicholson, G.A., Nassif, N., Storey, E., Macmillan, J.C., Collins, V., Williamson, R.S.B., Forrest, S.M., 1999, Clinical and genetic study of Friedreich ataxia in an Australian population, American Journal of Medical Genetics, vol 87, Wiley-Liss, Division of John Wiley & Sons Inc., New York NY USA, pp. 168-174.

Smith, M.J., Gardner, R.J., Knight, M.A., Forrest, S.M., Beyreuther, K., Storey, E., McLean, C.A., Cotton, R.G., Cappai, R., Masters, C.L., 1999, Early-onset Alzheimer's disease caused by a novel mutation at codon 219 of the presenilin-1 gene, NeuroReport, vol 10, Lippincott Williams & Wilkins, Philadelphia USA, pp. 503-507.

Storey, E., Forrest, S.M., Shaw, J.H., Mitchell, P., Gardner, R.J., 1999, Spinocerebellar ataxia type 2: Clinical features of a pedigree displaying prominent frontal-executive dysfunction, Archives of Neurology, vol 56, American Medical Association, Chicago USA, pp. 43-50.

Storey, E., Cappai, R., 1999, The amyloid precursor protein of Alzheimer's disease and the A-beta peptide, Neuropathology and Applied Neurobiology, vol 25, Blackwell Science Ltd, Oxford UK, pp. 81-97.

Storey, E., 1998, Dominantly inherited ataxias: Part 1, Journal of Clinical Neuroscience, vol 5 (3), Churchill Livingstone, Edinburgh UK, pp. 257-264.

Storey, E., 1998, Dominantly inherited ataxias: Part II, Journal of Clinical Neuroscience, vol 5 (4), Churchill Livingstone, Edinburgh UK, pp. 369-377.

Conference Proceedings

Elkadi, S., Storey, E., Krum, H., 2006, What specific domains of cognition are impaired in patients with chronic heart failure?, Journal of the American College of Cardiology (ACC 06 Abstracts), pp. 38-39.

Slavin, M.J., Mattingley, J.B., Bradshaw, J.L., Storey, E., 1999, Adjusting the spatial scale of selective attention in dementia of the Alzheimer's type, Australian Journal of Psychology, Leura NSW 7-10 October 1999, The Australian Psychological Society Ltd, Carlton Vic Australia, pp. 159-160.

Other

Storey, E., 2007, Spinocerebellar ataxia type 20, GeneReviews at GeneTests: Medical Genetics Information Resource [database online], vol journal, University of Washington, Seattle.

Storey, E., 2006, Spinocerebellar ataxia type 15, GeneReviews at GeneTests: Medical Genetics Information Resource [database online], vol journal, University of Washington, Seattle Washington USA.

Postgraduate Research Supervisions

Current Supervision

Program of Study:

(DOCTORATE BY RESEARCH).

Thesis Title:

Cerebellar disease: Exploring the application, reliability and validity of a diagnostic instrument for quantifying ataxia of the upper limbs.

Supervisors:

Storey, E (Main), Symmons, M (Associate).

Program of Study:

(DOCTORATE BY RESEARCH).

Thesis Title:

Establishing the role of serotonergic neurons in the emergence and maintenance of dyskinesias in Parkinsons' disease..

Supervisors:

Storey, E (Main), Williams, D (Associate).

Completed Supervision

Student:

Walsh, R.

Program of Study:

Differential proteolytic susceptibility and neuronal selectivity in the polyglutamine tract diseases. (PHD) 2005.

Supervisors:

Storey, E (Main).