Emily Swinkin
Overview
Explore the profile of Emily Swinkin including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
9
Citations
37
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0
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Recent Articles
1.
Reyes N, Bendahan N, Swinkin E, Lang A, Bassett A
Neurol Sci
. 2024 Jul;
46(1):463-468.
PMID: 39023712
Background: Williams syndrome (WS; chromosome 7q11.23 deletion) is a rare, multisystemic, neurodevelopmental disorder with variable penetrance and expressivity. Although movement and psychiatric disorders are known to occur in individuals with...
2.
Di Luca D, Gilmour G, Fearon C, Swinkin E, Freitas E, Kuhlman G, et al.
Mov Disord Clin Pract
. 2023 Jul;
10(7):1114-1119.
PMID: 37476317
Background: Pain is common in Parkinson's disease (PD), but effective therapies are limited. Objectives: To determine the maximum tolerated dose (MTD) and safety of formulations of delta-9-tetrahydrocannabinol (THC) and cannabidiol...
3.
Martinez-Valbuena I, Swinkin E, Santamaria E, Fernandez-Irigoyen J, Sackmann V, Kim A, et al.
Acta Neuropathol
. 2022 Jun;
144(2):167-185.
PMID: 35748929
Lewy body disorders (LBD), characterized by the deposition of misfolded α-synuclein (α-Syn), are clinically heterogeneous. Although the distribution of α-Syn correlates with the predominant clinical features, the burden of pathology...
4.
Di Luca D, Swinkin E, Lang A
Neurology
. 2022 Mar;
98(17):731-732.
PMID: 35277441
No abstract available.
5.
Swinkin E, Jabehdar Maralani P, Sundaram A
Can J Neurol Sci
. 2021 Apr;
49(2):278-281.
PMID: 33888167
Idiopathic intracranial hypertension (IIH) typically presents with bilateral papilledema; however, highly asymmetric and rare unilateral cases have been reported. We report three cases of IIH meeting modified Dandy criteria presenting...
6.
Swinkin E, Lizarraga K, Algarni M, Dominguez L, Baarbe J, Saravanamuttu J, et al.
Mov Disord
. 2020 Nov;
36(4):999-1005.
PMID: 33251639
Background: Celiac disease is associated with motor cortex hyperexcitability and neurological manifestations including cortical myoclonus. Electroencephalography abnormalities have been described, but no distinct pattern has been reported. Methods: We describe...
7.
Keith J, Swinkin E, Gao A, Alminawi S, Zhang M, McGoldrick P, et al.
Neurol Genet
. 2020 Feb;
6(1):e394.
PMID: 32042922
Objective: To present the postmortem neuropathologic report of a patient with a mutation exhibiting an amyotrophic lateral sclerosis (ALS) clinical phenotype. Methods: A 54-year-old man without significant medical history or...
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