Research publications

Alfred Health research outcomes are published in a wide range of peer reviewed journals. 

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Frontotemporal dementia and Parkinsonism linked to chromosome 17 in a young Australian patient with the G389R Tau mutation

Bermingham N, Cowie TF, Paine M, Storey E, McLean C

(2008), Neuropathol Appl Neurobiol, 34(3), 366-70

Late onset antibody-mediated rejection and endothelial localization of vascular endothelial growth factor are associated with development of cardiac allograft vasculopathy

Bayliss J, Bailey M, Leet A, Stein AN, Thomson NM, McLean CA

(2008), Transplantation, 86(7), 991-7

Endoplasmic reticulum stress and induction of the unfolded protein response in human sporadic amyotrophic lateral sclerosis

Atkin JD, Farg MA, Walker AK, McLean C, Tomas D, Horne MK

(2008), Neurobiol Dis, 30(3), 400-7

What is the "true" prevalence of female sexual dysfunctions and does the way we assess these conditions have an impact?

Hayes RD, Dennerstein L, Bennett CM, Fairley CK

(2008), J Sex Med, 5(4), 777-87

Risk factors for female sexual dysfunction in the general population: exploring factors associated with low sexual function and sexual distress

Hayes RD, Dennerstein L, Bennett CM, Sidat M, Gurrin LC, Fairley CK

(2008), J Sex Med, 5(7), 1681-93

HIV, viral hepatitis and STIs: a guide for primary care

Bradford D, Hoy J, Matthews G

(2008), ISBN 978-1-920773-50-2. Australasian Society for HIV Medicine, Sydney.,

Aspirin and Tranexamic Acid for Coronary Artery Surgery (ATACAS) Trial: rationale and design

Myles PS, Smith J, Knight J, Cooper DJ, Silbert B, McNeil J, Esmore DS, Buxton B, Krum H, Forbes A, Tonkin A; ATACAS Trial Group

(2008), Am Heart J, 155(2), 224-30

Gender differences in outcome in patients with hypotension and severe traumatic brain injury

Ponsford JL, Myles PS, Cooper DJ, McDermott FT, Murray LJ, Laidlaw J, Cooper G, Tremayne AB, Bernard SA

(2008), Injury, 39(1), 67-76

Paramedic tracheal intubation using the intubating laryngeal mask airway

McCall MJ, Reeves M, Skinner M, Ginifer C, Myles P, Dalwood N

(2008), Prehosp Emerg Care, 12(1), 30-4

Spinocerebellar ataxia type 20

Storey E

(2007), In: GeneTests: Medical Genetics Information Resource (database online). Copyright, University of Washington, Seattle. 1993-2008. Available at http://www.genetests.org. Accessed http://www.genetests.org June 2007,

Principles of neuropsychometric assessment

Storey E, Kinsella G

(2007), In: Schapira AH (ed). Neurology and Clinical Neuroscience. Mosby, Elsevier, USA, 22-30

The neglect syndrome

Storey E

(2007), In: Schapira AH (ed). Neurology and Clinical Neuroscience. Mosby, Elsevier, USA, 73-82

Executive function and its assessment

Kinsella GJ, Storey E, Crawford JR

(2007), In: Schapira AH (ed). Neurology and Clinical Neuroscience. Mosby, Elsevier, USA, 83-95

The ubiquitin-proteasome system in Huntington's disease and other polyglutamine diseases

Kelly L, Storey E

(2007), In: Di Napoli M, Wojcik C (eds). The Ubiquitin Proteasome System in the Central Nervous System: From Physiology to Pathology. Nova Science Publishers, USA, 793-812

Hydrocephalus including normal-pressure hydrocephalus

Kazemi NJ, Kaye AH, Storey E

(2007), In: Schapira AH (ed). Neurology and Clinical Neuroscience. Mosby, Elsevier, USA, 825-33

James Parkinson's London

Williams DR

(2007), Mov Disord, 22(13), 1857-9

Genetic variation at the tau locus and clinical syndromes associated with progressive supranuclear palsy

Williams DR, Pittman AM, Revesz T, Lees AJ, de Silva R

(2007), Mov Disord, 22(6), 895-7

Pure akinesia with gait freezing: a third clinical phenotype of progressive supranuclear palsy

Williams DR, Holton JL, Strand K, Revesz T, Lees AJ

(2007), Mov Disord, 22(15), 2235-41

Pathological tau burden and distribution distinguishes progressive supranuclear palsy-parkinsonism from Richardson's syndrome

Williams DR, Holton JL, Strand C, Pittman A, de Silva R, Lees AJ, Revesz T

(2007), Brain, 130(Pt 6), 1566-76

Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans

van de Leemput J, Chandran J, Knight MA, et al.

(2007), PLoS Genetics, 3(6), e108

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