Sarah A OShea
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Explore the profile of Sarah A OShea including associated specialties, affiliations and a list of published articles.
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13
Citations
75
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Recent Articles
1.
Xue C, Kowshik S, Lteif D, Puducheri S, Jasodanand V, Zhou O, et al.
Nat Med
. 2024 Jul;
30(10):2977-2989.
PMID: 38965435
Differential diagnosis of dementia remains a challenge in neurology due to symptom overlap across etiologies, yet it is crucial for formulating early, personalized management strategies. Here, we present an artificial...
2.
Xue C, Kowshik S, Lteif D, Puducheri S, Jasodanand V, Zhou O, et al.
medRxiv
. 2024 Apr;
PMID: 38585870
Differential diagnosis of dementia remains a challenge in neurology due to symptom overlap across etiologies, yet it is crucial for formulating early, personalized management strategies. Here, we present an AI...
3.
Schneider S, Desai S, Phokaewvarangkul O, Rosca E, Sringean J, Anand P, et al.
J Neurol
. 2023 Mar;
270(5):2409-2415.
PMID: 36943516
Background: Neurological symptoms are common manifestation in acute COVID-19. This includes hyper- and hypokinetic movement disorders. Data on their outcome, however, is limited. Methods: Cases with new-onset COVID-19-associated movement disorders...
4.
OShea S, Shih L
Semin Neurol
. 2023 Mar;
43(1):4-16.
PMID: 36893797
In this manuscript, we review the epidemiology of movement disorders including Parkinson's disease (PD), atypical parkinsonism, essential tremor, dystonia, functional movement disorders, tic disorders, chorea, and ataxias. We emphasize age-,...
5.
Hickman R, OShea S, Mehler M, Chung W
Nat Rev Neurol
. 2022 Jan;
18(2):117-124.
PMID: 34987232
Intellectual disability and autism spectrum disorder (ASD) are common, and genetic testing is increasingly performed in individuals with these diagnoses to inform prognosis, refine management and provide information about recurrence...
6.
OShea S, Hickman R, Cortes E, Vonsattel J, Fahn S, Okur V, et al.
Mov Disord
. 2021 Aug;
36(11):2681-2687.
PMID: 34415653
Background: PLXNA1 encodes for Plexin-A, a transmembrane protein expressed in the developing nervous system. Mutations in this gene have been associated with developmental delay but have not been previously associated...
7.
Dworschak G, Punetha J, Kalanithy J, Mingardo E, Erdem H, Akdemir Z, et al.
Genet Med
. 2021 May;
23(9):1715-1725.
PMID: 34054129
Purpose: To investigate the effect of PLXNA1 variants on the phenotype of patients with autosomal dominant and recessive inheritance patterns and to functionally characterize the zebrafish homologs plxna1a and plxna1b...
8.
Schindlbeck K, Gupta D, Tang C, OShea S, Poston K, Choi Y, et al.
Eur J Nucl Med Mol Imaging
. 2021 Apr;
48(11):3522-3529.
PMID: 33839891
Purpose: Up to 25% of patients diagnosed as idiopathic Parkinson's disease (IPD) have an atypical parkinsonian syndrome (APS). We had previously validated an automated image-based algorithm to discriminate between IPD,...
9.
Juul D, Gutmann L, Adams Jr H, OShea S, Faulkner L
Neurology
. 2020 Sep;
96(5):233-236.
PMID: 32913017
Objective: To obtain feedback from early career adult and pediatric neurologists about the psychiatry component of residency training. Methods: A survey was developed and administered electronically to 4 cohorts of...
10.
Wattiez A, OShea S, Ten Eyck P, Sowers L, Recober A, Russo A, et al.
Headache
. 2020 Jul;
60(8):1581-1591.
PMID: 32712960
Objective: To determine whether patients with vestibular migraine are more likely to suffer from an occipital headache than patients with migraine without vestibular symptoms. Background: Vestibular migraine is an underdiagnosed...