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Prion protein “gamma-cleavage”: characterizing a novel endoproteolytic processing event

Cellular and molecular life sciences : CMLS, 2016-02, Vol.73 (3), p.667-683

2016

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Prion disease in Indigenous Australians

Internal medicine journal, 2021-07, Vol.51 (7), p.1101-1105

2021

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Intra-cerebral haemorrhage but not neurodegenerative disease appears over-represented in deaths of Australian cadaveric pituitary hormone recipients

Journal of clinical neuroscience, 2020-11, Vol.81, p.78-82

2020

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Corrigendum to “Intra-cerebral haemorrhage but not neurodegenerative disease appears over-represented in deaths of Australian cadaveric pituitary hormone recipients” [J. Clin. Neurosci. 81 (2020) 78–82]

Journal of clinical neuroscience, 2020-11, Vol.81, p.447-447

2020

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Intensity of human prion disease surveillance predicts observed disease incidence

Journal of neurology, neurosurgery and psychiatry, 2013-12, Vol.84 (12), p.1372-1377

2013

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Extended period of asymptomatic prion disease after low dose inoculation: Assessment of detection methods and implications for infection control

Neurobiology of disease, 2005-11, Vol.20 (2), p.336-346

2005

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Lyodura use and the risk of iatrogenic Creutzfeldt–Jakob disease in Australia

Medical journal of Australia, 2004-02, Vol.180 (4), p.177-181

2004

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Increased Proportions of C1 Truncated Prion Protein Protect Against Cellular M1000 Prion Infection

Journal of neuropathology and experimental neurology, 2009-10, Vol.68 (10), p.1125-1135

2009

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Enhanced geographically restricted surveillance simulates sporadic Creutzfeldt-Jakob disease cluster

Brain (London, England : 1878), 2009-02, Vol.132 (2), p.493-501

2009

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The Prion Protein Preference of Sporadic Creutzfeldt-Jakob Disease Subtypes

The Journal of biological chemistry, 2012-10, Vol.287 (43), p.36465-36472

2012

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14-3-3 protein detection and sporadic CJD: the status quo serves well while awaiting progress

Journal of neurology, neurosurgery and psychiatry, 2010-11, Vol.81 (11), p.1181-1181

2010

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Correlative studies support lipid peroxidation is linked to PrP(res) propagation as an early primary pathogenic event in prion disease

Brain research bulletin, 2006-01, Vol.68 (5), p.346-354

2006

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Iatrogenic Creutzfeldt–Jakob disease in Australia: time to amend infection control measures for pituitary hormone recipients?

Medical journal of Australia, 2010-09, Vol.193 (6), p.366-369

2010

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No evidence for prion protein gene locus multiplication in Creutzfeldt-Jakob disease

Neuroscience letters, 2010-03, Vol.472 (1), p.16-18

2010

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Molecular typing of PrPres in human sporadic CJD brain tissue

Methods in molecular biology (Clifton, N.J.), 2008, Vol.459, p.241

2008

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β‐Amyloid protein oligomers induced by metal ions and acid pH are distinct from those generated by slow spontaneous ageing at neutral pH

European journal of biochemistry, 2003-11, Vol.270 (21), p.4282-4293

2003

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Surveillance of Creutzfeldt-Jakob disease in Australia: update to December 2011

Communicable diseases intelligence, 2012-06, Vol.36 (2), p.E174-E179

2012

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Surveillance of Creutzfeldt-Jakob disease in Australia: update to December 2010

Communicable diseases intelligence quarterly report, 2011-06, Vol.35 (2), p.149

2011

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Surveillance of Creutzfeldt-Jakob disease in Australia: 2010 update

Communicable diseases intelligence quarterly report, 2010-06, Vol.34 (2), p.96

2010

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Correlative studies support lipid peroxidation is linked to PrPres propagation as an early primary pathogenic event in prion disease

Brain research bulletin, 2006-01, Vol.68 (5), p.346-354

2006

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Surveillance of Creutzfeldt-Jakob disease in Australia: 2009 update

Communicable diseases intelligence quarterly report, 2009-06, Vol.33 (2), p.188

2009

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Creutzfeldt-Jakob disease surveillance in Australia: update to December 2014

Communicable diseases intelligence, 2016-06, Vol.40 (2), p.E207-E215

2016

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Creutzfeldt-Jakob disease surveillance in Australia: update to December 2015

Communicable diseases intelligence, 2016-09, Vol.40 (3), p.E368-E376

2016

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Creutzfeldt-Jakob disease surveillance in Australia, update to December 2013

Communicable diseases intelligence, 2014-12, Vol.38 (4), p.E348-E355

2014

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Surveillance for Creutzfeldt-Jakob disease in Australia: update to December 2012

Communicable diseases intelligence, 2013-06, Vol.37 (2), p.E115-E120

2013

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Prion protein “gamma-cleavage”: characterizing a novel endoproteolytic processing event

Prion disease in Indigenous Australians

Intra-cerebral haemorrhage but not neurodegenerative disease appears over-represented in deaths of Australian cadaveric pituitary hormone recipients

Corrigendum to “Intra-cerebral haemorrhage but not neurodegenerative disease appears over-represented in deaths of Australian cadaveric pituitary hormone recipients” [J. Clin. Neurosci. 81 (2020) 78–82]

Intensity of human prion disease surveillance predicts observed disease incidence

Extended period of asymptomatic prion disease after low dose inoculation: Assessment of detection methods and implications for infection control

Lyodura use and the risk of iatrogenic Creutzfeldt–Jakob disease in Australia

Increased Proportions of C1 Truncated Prion Protein Protect Against Cellular M1000 Prion Infection

Enhanced geographically restricted surveillance simulates sporadic Creutzfeldt-Jakob disease cluster

The Prion Protein Preference of Sporadic Creutzfeldt-Jakob Disease Subtypes

14-3-3 protein detection and sporadic CJD: the status quo serves well while awaiting progress

Correlative studies support lipid peroxidation is linked to PrP(res) propagation as an early primary pathogenic event in prion disease

Iatrogenic Creutzfeldt–Jakob disease in Australia: time to amend infection control measures for pituitary hormone recipients?

No evidence for prion protein gene locus multiplication in Creutzfeldt-Jakob disease

Molecular typing of PrPres in human sporadic CJD brain tissue

β‐Amyloid protein oligomers induced by metal ions and acid pH are distinct from those generated by slow spontaneous ageing at neutral pH

Surveillance of Creutzfeldt-Jakob disease in Australia: update to December 2011

Surveillance of Creutzfeldt-Jakob disease in Australia: update to December 2010

Surveillance of Creutzfeldt-Jakob disease in Australia: 2010 update

Correlative studies support lipid peroxidation is linked to PrPres propagation as an early primary pathogenic event in prion disease

Surveillance of Creutzfeldt-Jakob disease in Australia: 2009 update

Creutzfeldt-Jakob disease surveillance in Australia: update to December 2014

Creutzfeldt-Jakob disease surveillance in Australia: update to December 2015

Creutzfeldt-Jakob disease surveillance in Australia, update to December 2013

Surveillance for Creutzfeldt-Jakob disease in Australia: update to December 2012

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