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Attenuation Correction Synthesis for Hybrid PET-MR Scanners: Application to Brain Studies

IEEE transactions on medical imaging, 2014-12, Vol.33 (12), p.2332-2341

2014

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Pathogenic VCP Mutations Induce Mitochondrial Uncoupling and Reduced ATP Levels

Neuron (Cambridge, Mass.), 2013-04, Vol.78 (1), p.57-64

2013

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Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population

American journal of human genetics, 2013-03, Vol.92 (3), p.345-353

2013

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Central neurodegeneration in Kennedy’s disease accompanies peripheral motor dysfunction

Scientific reports, 2024-08, Vol.14 (1), p.18331-10, Article 18331

2024

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Longitudinal diffusion tensor imaging in frontotemporal dementia

Annals of neurology, 2015-01, Vol.77 (1), p.33-46

2015

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Brainstem Correlates of Pathological Laughter and Crying Frequency in ALS

Frontiers in neurology, 2021-07, Vol.12, p.704059-704059

2021

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Structural neuroanatomy of tinnitus and hyperacusis in semantic dementia

Journal of neurology, neurosurgery and psychiatry, 2011-11, Vol.82 (11), p.1274-1278

2011

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Assessment of suspected motor neuron disease

BMJ (Online), 2022-11, p.e073857

2022

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Factors That Influence Non-Motor Impairment Across the ALS-FTD Spectrum: Impact of Phenotype, Sex, Age, Onset and Disease Stage

Frontiers in neurology, 2021-11, Vol.12, p.743688-743688

2021

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White matter tract signatures of impaired social cognition in frontotemporal lobar degeneration

NeuroImage clinical, 2015-01, Vol.8 (C), p.640-651

2015

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Behavioural changes predict poorer survival in amyotrophic lateral sclerosis

Brain and cognition, 2021-06, Vol.150, p.105710-105710, Article 105710

2021

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Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

Brain (London, England : 1878), 2012-03, Vol.135 (Pt 3), p.736-750

2012

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Mills Syndrome: Clinical and Radiologic Asymmetry

Neurology, 2021-04, Vol.96 (14), p.677-678

2021

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Assessing preparedness for Alzheimer disease‐modifying therapies in Australasian health care systems

Medical journal of Australia, 2023-04, Vol.218 (6), p.247-249

2023

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Developmental regulation of tau splicing is disrupted in stem cell-derived neurons from frontotemporal dementia patients with the 10 + 16 splice-site mutation in MAPT

Human molecular genetics, 2015-09, Vol.24 (18), p.5260-5269

2015

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The contribution of brain banks to knowledge discovery in amyotrophic lateral sclerosis: A systematic review

Neuropathology and applied neurobiology, 2022-12, Vol.48 (7), p.e12845-n/a

2022

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The impact of cognitive and behavioral impairment in amyotrophic lateral sclerosis

Expert review of neurotherapeutics, 2020-03, Vol.20 (3), p.281-293

2020

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Expanding the availability of medications for amyotrophic lateral sclerosis in Australia

Medical journal of Australia, 2020-03, Vol.212 (4), p.189-189.e1

2020

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Pathophysiology and Treatment of Non-motor Dysfunction in Amyotrophic Lateral Sclerosis

CNS drugs, 2021-05, Vol.35 (5), p.483-505

2021

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Novel approaches to assessing upper motor neuron dysfunction in motor neuron disease/amyotrophic lateral sclerosis: IFCN handbook chapter

Clinical neurophysiology, 2024-07, Vol.163, p.68-89

2024

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Profiles of white matter tract pathology in frontotemporal dementia

Human brain mapping, 2014-08, Vol.35 (8), p.4163-4179

2014

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Flavour identification in frontotemporal lobar degeneration

Journal of neurology, neurosurgery and psychiatry, 2013-01, Vol.84 (1), p.88-93

2013

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White matter tract signatures of the progressive aphasias

Neurobiology of aging, 2013-06, Vol.34 (6), p.1687-1699

2013

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A novel phenotype of hereditary spastic paraplegia type 7 associated with a compound heterozygous mutation in paraplegin

Muscle & nerve, 2020-07, Vol.62 (1), p.E44-E45

2020

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R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia

Alzheimer's & dementia, 2014-11, Vol.10 (6), p.602-608.e4

2014

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Attenuation Correction Synthesis for Hybrid PET-MR Scanners: Application to Brain Studies

Pathogenic VCP Mutations Induce Mitochondrial Uncoupling and Reduced ATP Levels

Large C9orf72 Hexanucleotide Repeat Expansions Are Seen in Multiple Neurodegenerative Syndromes and Are More Frequent Than Expected in the UK Population

Central neurodegeneration in Kennedy’s disease accompanies peripheral motor dysfunction

Longitudinal diffusion tensor imaging in frontotemporal dementia

Brainstem Correlates of Pathological Laughter and Crying Frequency in ALS

Structural neuroanatomy of tinnitus and hyperacusis in semantic dementia

Assessment of suspected motor neuron disease

Factors That Influence Non-Motor Impairment Across the ALS-FTD Spectrum: Impact of Phenotype, Sex, Age, Onset and Disease Stage

White matter tract signatures of impaired social cognition in frontotemporal lobar degeneration

Behavioural changes predict poorer survival in amyotrophic lateral sclerosis

Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features

Mills Syndrome: Clinical and Radiologic Asymmetry

Assessing preparedness for Alzheimer disease‐modifying therapies in Australasian health care systems

Developmental regulation of tau splicing is disrupted in stem cell-derived neurons from frontotemporal dementia patients with the 10 + 16 splice-site mutation in MAPT

The contribution of brain banks to knowledge discovery in amyotrophic lateral sclerosis: A systematic review

The impact of cognitive and behavioral impairment in amyotrophic lateral sclerosis

Expanding the availability of medications for amyotrophic lateral sclerosis in Australia

Pathophysiology and Treatment of Non-motor Dysfunction in Amyotrophic Lateral Sclerosis

Novel approaches to assessing upper motor neuron dysfunction in motor neuron disease/amyotrophic lateral sclerosis: IFCN handbook chapter

Profiles of white matter tract pathology in frontotemporal dementia

Flavour identification in frontotemporal lobar degeneration

White matter tract signatures of the progressive aphasias

A novel phenotype of hereditary spastic paraplegia type 7 associated with a compound heterozygous mutation in paraplegin

R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia

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