Richard A Walsh
Overview
Explore the profile of Richard A Walsh including associated specialties, affiliations and a list of published articles.
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Articles
37
Citations
392
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Recent Articles
1.
Donlon E, OKeeffe C, Horan J, Ruggieri F, Fitzpatrick J, ONeill M, et al.
Mov Disord Clin Pract
. 2025 Mar;
PMID: 40088078
No abstract available.
2.
Donlon E, Abdullah S, Ronan F, Garvey M, Austin N, Reynolds E, et al.
J Neurol
. 2024 Jul;
271(9):6377-6381.
PMID: 39030457
No abstract available.
3.
Menon P, Yi T, Moran S, Walsh R, Murphy S, Bogdanova-Mihaylova P
Cerebellum
. 2023 Nov;
23(4):1328-1337.
PMID: 38010570
Inherited cerebellar ataxias (CA) are heterogeneous progressive neurological conditions associated with significant functional limitations. This study aimed to assess the implications of inherited CA on patients' self-reported quality of life...
4.
Offiah C, Tierney S, Egan B, Collins R, Ryan D, McCarthy A, et al.
Ir J Med Sci
. 2023 Jun;
193(1):541.
PMID: 37269449
No abstract available.
5.
Offiah C, Tierney S, Egan B, Collins R, Ryan D, McCarthy A, et al.
Ir J Med Sci
. 2023 Apr;
192(6):3051-3062.
PMID: 37081289
Background/aims: Data are limited on the frequency of 'consensus decisions' between sub-specialists attending a neurovascular multidisciplinary meeting (MDM) regarding management of patients with extracranial carotid/vertebral stenoses and post-MDM 'adherence' to...
6.
7.
Bogdanova-Mihaylova P, Plapp H, Chen H, Early A, Cassidy L, Walsh R, et al.
Tomography
. 2021 Dec;
7(4):915-931.
PMID: 34941648
Ocular abnormalities occur frequently in Friedreich's ataxia (FRDA), although visual symptoms are not always reported. We evaluated a cohort of patients with FRDA to characterise the clinical phenotype and optic...
8.
Kelly M, Bogdanova-Mihaylova P, Skeens J, Moran S, Farrelly S, Walsh R, et al.
Cerebellum
. 2021 Jul;
21(2):280-296.
PMID: 34228323
Inherited ataxias are a heterogenous group of neurodegenerative disorders characterised by progressive impairment of balance and coordination, typically leading to permanent and progressive disability. Diagnosis and management of these disorders...
9.
Bogdanova-Mihaylova P, Chen H, Plapp H, Gorman C, Alexander M, McHugh J, et al.
J Neurol
. 2021 May;
268(10):3908.
PMID: 34014344
No abstract available.
10.
Bogdanova-Mihaylova P, Chen H, Plapp H, Gorman C, Alexander M, McHugh J, et al.
J Neurol
. 2021 Mar;
268(10):3897-3907.
PMID: 33774748
Background: Mutations in SPG7 are increasingly identified as a common cause of spastic ataxia. We describe a cohort of Irish patients with recessive SPG7-associated phenotype. Methods: Comprehensive phenotyping was performed...