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Closing the tau loop: the missing tau mutation

Brain (London, England : 1878), 2015-10, Vol.138 (Pt 10), p.3100-3109

2015

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Association Between Glucocerebrosidase Mutations and Parkinson's Disease in Ireland

Frontiers in neurology, 2020-06, Vol.11, p.527-527

2020

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Genetics of Frontotemporal Dementia

Current Neurology and Neuroscience Reports, 2016-12, Vol.16 (12), p.107-107, Article 107

2016

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Endoplasmic Reticulum Proteostasis/Protein Trafficking Enhancement: A Novel Synergistic Approach to Tackling α‐Synuclein

Movement disorders, 2022-09, Vol.37 (9), p.1803-1805

2022

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Dancing Feet Dyskinesia in a Patient with GBA-PD

Journal Of Movement Disorders, 2022, 15(1), , pp.83-85

2022

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The Role of Insular Cortex in Gut‐Inflammation Memory: What Does It Mean for Parkinson's Disease?

Movement disorders, 2022-04, Vol.37 (4), p.700-701

2022

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“Opening” New Insights Into LRRK2 Conformation and the Microtubule

Movement disorders, 2020-12, Vol.35 (12), p.2162-2163

2020

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Nature's Parkin experiment: Nix—a novel protective mechanism in Parkinson's disease

Movement disorders, 2017-07, Vol.32 (7), p.992-992

2017

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Initiating dopamine agonists rather than levodopa in early Parkinson's disease does not delay the need for deep brain stimulation

European journal of neurology, 2022-12, Vol.29 (12), p.3742-3747

2022

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PINK1, parkin, and autophagy receptors: A new model of mitophagy

Movement disorders, 2016-11, Vol.31 (11), p.1628-1629

2016

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Combining Skin α‐Synuclein Real‐Time Quaking‐Induced Conversion and Circulating Neurofilament Light Chain to Distinguish Multiple System Atrophy and Parkinson's Disease

Movement disorders, 2022-03, Vol.37 (3), p.648-650

2022

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The definition of precision medicine in neurodegenerative disorders and the one disease-many diseases tension

Handbook of Clinical Neurology, 2023, Vol.192, p.3-20

2023

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MUL1-A new potential for a therapeutic target for Parkinson's disease a commentary on "MUL1 acts in parallel to the PINK1/parkin pathway in regulating mitofusin and compensates for loss of PINK1/parkin" by Yun and colleagues (eLife 2014; 3: 1-26)

Movement disorders, 2016-07, Vol.31 (7), p.1037-1037

2016

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Is PARK10 a Locus for Familial PD? Yes or No?

Movement disorders, 2016-07, Vol.31 (7), p.970-970

2016

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A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene

Neurobiology of aging, 2021-10, Vol.106, p.343.e1-343.e8

2021

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Dystonia as complication of thalamic neurosurgery

Parkinsonism & related disorders, 2019-09, Vol.66, p.232-236

2019

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Commentary: Parkinson's Disease Genes VPS35 and EIF4G1 Interact Genetically and Converge on α-Synuclein

Frontiers in neuroscience, 2016-04, Vol.10, p.162-162

2016

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Extending the Phenotypic Spectrum Associated with STUB1 Mutations: A Case of Dystonia

Movement disorders clinical practice (Hoboken, N.J.), 2020-04, Vol.7 (3), p.318-324

2020

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PARKIN, PINK1, and DJ1 analysis in early-onset Parkinson’s disease in Ireland

Irish journal of medical science, 2022-04, Vol.191 (2), p.901-907

2022

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Cathepsin B p.Gly284Val Variant in Parkinson's Disease Pathogenesis

International journal of molecular sciences, 2022-06, Vol.23 (13), p.7086

2022

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Reply to STUB1‐Related Ataxias: A Challenging Diagnosis

Movement disorders clinical practice (Hoboken, N.J.), 2020-08, Vol.7 (6), p.735-736

2020

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Exacerbation of Stiff Person Syndrome by Selective Serotonin Reuptake Inhibitors

Movement disorders clinical practice (Hoboken, N.J.), 2021-07, Vol.8 (5), p.772-774

2021

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Micrographia following bilateral subthalamic nucleus deep brain stimulation

Parkinsonism & related disorders, 2016-07, Vol.28, p.161-162

2016

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Periodic Limb Movements while Awake (PLMA) as a Manifestation of Wearing‐Off in Parkinson's Disease: A Case Series and Review of the Literature

Movement disorders clinical practice (Hoboken, N.J.), 2022-07, Vol.9 (5), p.652-658

2022

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Closing the tau loop: the missing tau mutation

Association Between Glucocerebrosidase Mutations and Parkinson's Disease in Ireland

Genetics of Frontotemporal Dementia

Endoplasmic Reticulum Proteostasis/Protein Trafficking Enhancement: A Novel Synergistic Approach to Tackling α‐Synuclein

Dancing Feet Dyskinesia in a Patient with GBA-PD

The Role of Insular Cortex in Gut‐Inflammation Memory: What Does It Mean for Parkinson's Disease?

“Opening” New Insights Into LRRK2 Conformation and the Microtubule

Nature's Parkin experiment: Nix—a novel protective mechanism in Parkinson's disease

Initiating dopamine agonists rather than levodopa in early Parkinson's disease does not delay the need for deep brain stimulation

PINK1, parkin, and autophagy receptors: A new model of mitophagy

Combining Skin α‐Synuclein Real‐Time Quaking‐Induced Conversion and Circulating Neurofilament Light Chain to Distinguish Multiple System Atrophy and Parkinson's Disease

The definition of precision medicine in neurodegenerative disorders and the one disease-many diseases tension

MUL1-A new potential for a therapeutic target for Parkinson's disease a commentary on "MUL1 acts in parallel to the PINK1/parkin pathway in regulating mitofusin and compensates for loss of PINK1/parkin" by Yun and colleagues (eLife 2014; 3: 1-26)

Corrigendum to: A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823–10 G>T at the intron 9/exon 10 of the MAPT gene

Is PARK10 a Locus for Familial PD? Yes or No?

A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene

Dystonia as complication of thalamic neurosurgery

Commentary: Parkinson's Disease Genes VPS35 and EIF4G1 Interact Genetically and Converge on α-Synuclein

Extending the Phenotypic Spectrum Associated with STUB1 Mutations: A Case of Dystonia

PARKIN, PINK1, and DJ1 analysis in early-onset Parkinson’s disease in Ireland

Cathepsin B p.Gly284Val Variant in Parkinson's Disease Pathogenesis

Reply to STUB1‐Related Ataxias: A Challenging Diagnosis

Exacerbation of Stiff Person Syndrome by Selective Serotonin Reuptake Inhibitors

Micrographia following bilateral subthalamic nucleus deep brain stimulation

Periodic Limb Movements while Awake (PLMA) as a Manifestation of Wearing‐Off in Parkinson's Disease: A Case Series and Review of the Literature

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