Patricia McNamara
Overview
Explore the profile of Patricia McNamara including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
765
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0
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Recent Articles
1.
Chiaro G, Stancanelli C, Koay S, Vichayanrat E, Sander L, Ingle G, et al.
Clin Auton Res
. 2024 May;
34(3):341-352.
PMID: 38769233
Background: The cardiomyopathic and neuropathic phenotype of hereditary transthyretin amyloidosis are well recognized. Cardiovascular autonomic dysfunction is less systematically and objectively assessed. Methods: Autonomic and clinical features, quantitative cardiovascular autonomic...
2.
Herbell K, McNamara P, Cresswell C, Price M, Sweeney M, Bellonci C
Resid Treat Child Youth
. 2024 Jan;
41(1):2-23.
PMID: 38186636
This study presents a tiered conceptualization of family partnership developed by the Family-Run Executive Director Leadership Association (FREDLA) with examples of strategies from the literature. This sub-study was part of...
3.
Callanan E, McNamara P, Ingle G
Pract Neurol
. 2023 Dec;
24(2):116-120.
PMID: 38160054
A 62-year-old man attended ophthalmology for a simple ptosis repair. He had a chronic cough, a Horner's syndrome with post-gustatory hyperhidrosis. He was referred to the respiratory and neurology teams....
4.
Alnasser Alsukhni R, Vichayanrat E, Koay S, Davis L, Ingle G, McNamara P, et al.
Eur J Neurol
. 2023 Dec;
31(3):e16169.
PMID: 38085264
Background And Purpose: Pure autonomic failure (PAF) is a rare progressive neurodegenerative disease characterized by neurogenic orthostatic hypotension at presentation, without other neurological abnormalities. Some patients may develop other central...
5.
Bharucha T, Brown R, Marcoci C, Benjamin L, Hoskote C, McNamara P, et al.
J Neurol Sci
. 2023 Oct;
453:120771.
PMID: 37793287
Background: Patients with suspected encephalitis continue to represent a diagnostic and therapeutic challenge, even in highly resourced centres. In February 2018, we set up a monthly in-person multidisciplinary team meeting...
6.
Brown R, Benjamin L, Lunn M, Bharucha T, Zandi M, Hoskote C, et al.
BMJ
. 2023 Aug;
382:e073923.
PMID: 37595965
Although neurological complications of SARS-CoV-2 infection are relatively rare, their potential long term morbidity and mortality have a significant impact, given the large numbers of infected patients. Covid-19 is now...
7.
Heightman M, Prashar J, Hillman T, Marks M, Livingston R, Ridsdale H, et al.
BMJ Open Respir Res
. 2021 Nov;
8(1).
PMID: 34764200
Introduction: Post-COVID-19 complications require simultaneous characterisation and management to plan policy and health system responses. We describe the 12-month experience of the first UK dedicated post-COVID-19 clinical service to include...
8.
Bogdanova-Mihaylova P, McNamara P, Burton-Jones S, Murphy S
BMJ Case Rep
. 2021 Oct;
14(10).
PMID: 34706912
Hereditary motor and sensory neuropathy with agenesis of the corpus callosum (HMSN/ACC) is a rare autosomal recessive condition characterised by early-onset severe progressive neuropathy, variable degrees of ACC and cognitive...
9.
Koay S, Vichayanrat E, Bremner F, Panicker J, Lang B, Lunn M, et al.
Ann Neurol
. 2021 Jan;
89(4):753-768.
PMID: 33438240
Objective: The objective of this study was to evaluate patients with ganglionic acetylcholine receptor antibody (gAChR-Ab) positive autoimmune autonomic ganglionopathy using a multimodal testing protocol to characterize their full clinical...
10.
Paterson R, Brown R, Vivekanandam V, Foulkes A, Thom M, Wiethoff S, et al.
Brain
. 2020 Dec;
143(12):e101.
PMID: 33324968
No abstract available.