Conor Fearon

Canada

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Articles (11)

Year:

2022

Year:

2022

Year:

2022

Year:

2021

Year:

2021

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2021

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2021

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2021

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2021

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2021

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2020

Collaborators (7)

Isabelle Killane

Lecturer

Technological University Dublin

IRELAND

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Alfonso Fasano

CANADA

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Simon Kelly

Professor

Dublin City University

IRELAND

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John Butler

Lecturer

Technological University Dublin

IRELAND

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zhou zhou

KTH Royal Institute of Technology

SWEDEN

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Taku Hatano

Associate Professor

Juntendo University

JAPAN

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John Mulvihill

Lecturer in Biomedical Engineering

University of Limerick

IRELAND

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Conor Fearon

Research Interests

Explore related searches

Contact this professor

Articles (11)

Neuroimaging Pearls from the MDS Congress Video Challenge. Part 2: Acquired Disorders

Movement Disorders and<scp>SARS‐CoV</scp>‐2

Neuroimaging Pearls from the MDS Congress Video Challenge. Part 1: Genetic Disorders

Mechanical characterisation of the human dura mater, falx cerebri and superior sagittal sinus

Recurrent Hypothalamic Dysfunction in Seropositive Neuromyelitis Optica.

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

Angioleiomyoma arising from a thoracic vertebra

On the emergence of tremor in prodromal Parkinson's disease

Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by MAPT Variants

Parkinson's Disease and COVID-19: Do We Need to Be More Patient?

Neurophysiological correlates of dual tasking in people with Parkinson's disease and freezing of gait.

Collaborators (7)

Isabelle Killane

Alfonso Fasano

Simon Kelly

John Butler

zhou zhou

Taku Hatano

John Mulvihill

Make your next move.

Conor Fearon

Research Interests

Explore related searches

Contact this professor

Articles (11)

Neuroimaging Pearls from the MDS Congress Video Challenge. Part 2: Acquired Disorders

Movement Disorders and<scp>SARS‐CoV</scp>‐2

Neuroimaging Pearls from the MDS Congress Video Challenge. Part 1: Genetic Disorders

Mechanical characterisation of the human dura mater, falx cerebri and superior sagittal sinus

Recurrent Hypothalamic Dysfunction in Seropositive Neuromyelitis Optica.

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

Angioleiomyoma arising from a thoracic vertebra

On the emergence of tremor in prodromal Parkinson's disease

Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by MAPT Variants

Parkinson's Disease and COVID-19: Do We Need to Be More Patient?

Neurophysiological correlates of dual tasking in people with Parkinson's disease and freezing of gait.

Collaborators (7)

Isabelle Killane

Alfonso Fasano

Simon Kelly

John Butler

zhou zhou

Taku Hatano

John Mulvihill

Make your next move.

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