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Coexisting Lewy body disease and clinical parkinsonism in amyotrophic lateral sclerosis

European journal of neurology, 2021-07, Vol.28 (7), p.2192-2199

2021

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Diffusion kurtosis and quantitative susceptibility mapping MRI are sensitive to structural abnormalities in amyotrophic lateral sclerosis

NeuroImage clinical, 2019-01, Vol.24, p.101953-101953, Article 101953

2019

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Genetic Analysis of Tryptophan Metabolism Genes in Sporadic Amyotrophic Lateral Sclerosis

Frontiers in immunology, 2021-06, Vol.12, p.701550

2021

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Heterogeneity of cortical pTDP-43 inclusion morphologies in amyotrophic lateral sclerosis

Acta neuropathologica communications, 2023-11, Vol.11 (1), p.1-180, Article 180

2023

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Inflammasome inhibition prevents α-synuclein pathology and dopaminergic neurodegeneration in mice

Science translational medicine, 2018-10, Vol.10 (465)

2018

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Increased peripheral inflammation in asymptomatic leucine-rich repeat kinase 2 mutation carriers

Movement disorders, 2016-06, Vol.31 (6), p.889-897

2016

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Measurement of LRRK2 and Ser910/935 phosphorylated LRRK2 in peripheral blood mononuclear cells from idiopathic Parkinson's disease patients

Journal of Parkinson's disease, 2013, Vol.3 (2), p.145-152

2013

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Limitations of Electromyography in the Assessment of Abdominal Wall Muscle Contractility Following Botulinum Toxin A Injection

Frontiers in surgery, 2019-04, Vol.6, p.16-16

2019

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The phenotypic spectrum of dystonia in Mohr-Tranebjaerg syndrome

Movement disorders, 2012-07, Vol.27 (8), p.1034-1040

2012

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Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis

Journal of medical genetics, 2021-02, Vol.58 (2), p.87-95

2021

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The importance of patient‐centred drug development for amyotrophic lateral sclerosis

Neuropathology and applied neurobiology, 2023-12, Vol.49 (6), p.e12944-n/a

2023

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RNA sequencing of peripheral blood in amyotrophic lateral sclerosis reveals distinct molecular subtypes: Considerations for biomarker discovery

Neuropathology and applied neurobiology, 2023-12, Vol.49 (6), p.e12943-n/a

2023

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Predictive genetic testing for amyotrophic lateral sclerosis and frontotemporal dementia: genetic counselling considerations

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2017-10, Vol.18 (7-8), p.475-485

2017

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Safety and tolerability of Triumeq in amyotrophic lateral sclerosis: the Lighthouse trial

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2019-10, Vol.20 (7-8), p.595-604

2019

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Riluzole is associated with decreasing neuritic plaque severity in amyotrophic lateral sclerosis

Brain (London, England : 1878), 2023-03, Vol.146 (3), p.e17-e19

2023

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Short tandem repeat expansions in LRP12 are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestry

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-08, Vol.25 (5-6), p.644-647

2024

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Involvement of quinolinic acid in the neuropathogenesis of amyotrophic lateral sclerosis

Neuropharmacology, 2017-01, Vol.112 (Pt B), p.346-364

2017

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Metabolite Profiling Reveals Predictive Biomarkers and the Absence of β‑Methyl Amino‑l‑alanine in Plasma from Individuals Diagnosed with Amyotrophic Lateral Sclerosis

Journal of proteome research, 2020-08, Vol.19 (8), p.3276-3285

2020

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A possible role for humoral immunity in the pathogenesis of Parkinson's disease

Brain (London, England : 1878), 2005-11, Vol.128 (11), p.2665-2674

2005

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C9orf72-Associated Dipeptide Repeat Expansions Perturb ER-Golgi Vesicular Trafficking, Inducing Golgi Fragmentation and ER Stress, in ALS/FTD

Molecular neurobiology, 2024-05

2024

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3033 Poliomyelitis sixty years prior to amyotrophic lateral sclerosis

BMJ neurology open, 2024-08, Vol.6 (Suppl 1), p.A20-A21

2024

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Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression

Scientific reports, 2019-06, Vol.9 (1), p.8254-8254, Article 8254

2019

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Genetic analysis of GLT8D1 and ARPP21 in Australian familial and sporadic amyotrophic lateral sclerosis

Neurobiology of aging, 2021-05, Vol.101, p.297.e9-297.e11

2021

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NEK1 and STMN2 short tandem repeat lengths are not associated with Australian amyotrophic lateral sclerosis risk

Neurobiology of aging, 2022-08, Vol.116, p.92-95

2022

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Coexisting Lewy body disease and clinical parkinsonism in amyotrophic lateral sclerosis

Diffusion kurtosis and quantitative susceptibility mapping MRI are sensitive to structural abnormalities in amyotrophic lateral sclerosis

Genetic Analysis of Tryptophan Metabolism Genes in Sporadic Amyotrophic Lateral Sclerosis

Heterogeneity of cortical pTDP-43 inclusion morphologies in amyotrophic lateral sclerosis

Inflammasome inhibition prevents α-synuclein pathology and dopaminergic neurodegeneration in mice

Increased peripheral inflammation in asymptomatic leucine-rich repeat kinase 2 mutation carriers

Measurement of LRRK2 and Ser910/935 phosphorylated LRRK2 in peripheral blood mononuclear cells from idiopathic Parkinson's disease patients

Limitations of Electromyography in the Assessment of Abdominal Wall Muscle Contractility Following Botulinum Toxin A Injection

The phenotypic spectrum of dystonia in Mohr-Tranebjaerg syndrome

Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis

The importance of patient‐centred drug development for amyotrophic lateral sclerosis

RNA sequencing of peripheral blood in amyotrophic lateral sclerosis reveals distinct molecular subtypes: Considerations for biomarker discovery

Predictive genetic testing for amyotrophic lateral sclerosis and frontotemporal dementia: genetic counselling considerations

Safety and tolerability of Triumeq in amyotrophic lateral sclerosis: the Lighthouse trial

Riluzole is associated with decreasing neuritic plaque severity in amyotrophic lateral sclerosis

Short tandem repeat expansions in LRP12 are absent in cohorts of familial and sporadic amyotrophic lateral sclerosis patients of European ancestry

Involvement of quinolinic acid in the neuropathogenesis of amyotrophic lateral sclerosis

Metabolite Profiling Reveals Predictive Biomarkers and the Absence of β‑Methyl Amino‑l‑alanine in Plasma from Individuals Diagnosed with Amyotrophic Lateral Sclerosis

A possible role for humoral immunity in the pathogenesis of Parkinson's disease

C9orf72-Associated Dipeptide Repeat Expansions Perturb ER-Golgi Vesicular Trafficking, Inducing Golgi Fragmentation and ER Stress, in ALS/FTD

Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics

3033 Poliomyelitis sixty years prior to amyotrophic lateral sclerosis

Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression

Genetic analysis of GLT8D1 and ARPP21 in Australian familial and sporadic amyotrophic lateral sclerosis

NEK1 and STMN2 short tandem repeat lengths are not associated with Australian amyotrophic lateral sclerosis risk

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