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McCarthy, Allan

A5110915610 | I2803035300

Mayo Clinic

Tallaght University Hospital

Citations 7

The Assessment of RAB32 p.Ser71Arg Variant Prevalence in Parkinson’s Disease across African, European, and South American Cohorts. (P6-16.010)

Neurology | June 10, 2026 | Volume: 106 | Issue: 11_Supplement_1 | Pages: No page available

10.1212/wnl.0000000000213183

The Assessment of RAB32 p. Ser71Arg Variant Prevalence in Parkinson's Disease Across Selected African, European, and South American Cohorts

Movement Disorders | January 16, 2026 | Volume: 41 | Issue: 4 | Pages: 1016-1019

10.1002/mds.70175 | PMID 41542720

Association between glucocerebrosidase mutations and Parkinson’s disease in Ireland (S53.003)

Neurology | December 7, 2023 | Volume: 92 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.92.15_supplement.s53.003

Qualitative and quantitative measurement of skin surface fatty acids in Parkinson’s disease-the results of the first case-control study in any neurological condition. (2581)

Neurology | December 7, 2023 | Volume: 94 | Issue: 15_supplement | Pages: No page available

10.1212/wnl.94.15_supplement.2581

Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders

Neurology | November 11, 2015 | Volume: 85 | Issue: 23 | Pages: 2016-2025

10.1212/wnl.0000000000002170 | PMID 26561290

Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies

Neurology | September 3, 2015 | Volume: 85 | Issue: 19 | Pages: 1680-1686

10.1212/wnl.0000000000001946 | PMID 26333800

Asymmetrical leg atrophy in levodopa‐responsive dystonia due to a novel GTP cyclohydrolase mutation

Movement Disorders | January 28, 2014 | Volume: 29 | Issue: 3 | Pages: 425-426

10.1002/mds.25813 | PMID 24474670