Priya Gami-Patel
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Explore the profile of Priya Gami-Patel including associated specialties, affiliations and a list of published articles.
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10
Citations
97
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Recent Articles
1.
Dijkstra A, Morrema T, Hart de Ruyter F, Gami-Patel P, Verbraak F, de Boer J, et al.
Acta Neuropathol
. 2023 Aug;
146(5):767-770.
PMID: 37597044
No abstract available.
2.
Fiondella L, Gami-Patel P, Blok C, Rozemuller A, Hoozemans J, Pijnenburg Y, et al.
Acta Neuropathol Commun
. 2023 Apr;
11(1):63.
PMID: 37046309
Movement disorders (MD) have been linked to degeneration of the substantia nigra (SN) in Parkinson's disease and include bradykinesia, rigidity, and tremor. They are also present in frontotemporal dementia (FTD),...
3.
Gami-Patel P, Scarioni M, Bouwman F, Boon B, Van Swieten J, Bank N, et al.
Neuropathol Appl Neurobiol
. 2022 Feb;
48(4):e12798.
PMID: 35152451
Aims: The loss of von Economo neurons (VENs) and GABA receptor subunit theta (GABRQ) containing neurons is linked to early changes in social-emotional cognition and is seen in frontotemporal dementia...
4.
Scarioni M, Gami-Patel P, Peeters C, de Koning F, Seelaar H, Mol M, et al.
Brain
. 2022 Feb;
146(1):307-320.
PMID: 35136978
Three subtypes of distinct pathological proteins accumulate throughout multiple brain regions and shape the heterogeneous clinical presentation of frontotemporal lobar degeneration (FTLD). Besides the main pathological subtypes, co-occurring pathologies are...
5.
Dijkstra A, Gami-Patel P, Rozemuller A, Bugiani M, Pijnenburg Y, Smit G, et al.
Schizophr Res
. 2020 Nov;
228:611-613.
PMID: 33243715
No abstract available.
6.
Gami-Patel P, van Dijken I, Meeter L, Melhem S, Morrema T, Scheper W, et al.
Brain Pathol
. 2020 Sep;
31(1):163-173.
PMID: 32865835
A repeat expansion in the C9orf72 gene is the most prevalent genetic cause of frontotemporal dementia (C9-FTD). Several studies have indicated the involvement of the unfolded protein response (UPR) in...
7.
Scarioni M, Gami-Patel P, Timar Y, Seelaar H, Van Swieten J, Rozemuller A, et al.
Ann Neurol
. 2020 Apr;
87(6):950-961.
PMID: 32281118
Objective: The pathology of frontotemporal dementia, termed frontotemporal lobar degeneration (FTLD), is characterized by distinct molecular classes of aggregated proteins, the most common being TAR DNA-binding protein-43 (TDP-43), tau, and...
8.
Gittings L, Foti S, Benson B, Gami-Patel P, Isaacs A, Lashley T
Acta Neuropathol Commun
. 2019 Feb;
7(1):18.
PMID: 30755280
Frontotemporal lobar degeneration (FTLD) is pathologically subdivided based on the presence of particular pathological proteins that are identified in inclusion bodies observed post-mortem. The FTLD-FUS subgroup is defined by the...
9.
Murray C, Gami-Patel P, Gkanatsiou E, Brinkmalm G, Portelius E, Wirths O, et al.
Acta Neuropathol Commun
. 2018 Jul;
6(1):62.
PMID: 30029687
In the majority of affected brain regions the pathological hallmarks of Alzheimer's disease (AD) are β-amyloid (Aβ) deposits in the form of diffuse and neuritic plaques, tau pathology in the...
10.
Gami-Patel P, Bandopadhyay R, Brelstaff J, Revesz T, Lashley T
Neurobiol Aging
. 2016 Aug;
46:192-203.
PMID: 27500866
Frontotemporal lobar degeneration with fused in sarcoma-positive inclusions (FTLD-FUS) is a disease with unknown cause. Transportin 1 is abundantly found in FUS-positive inclusions and responsible for the nuclear import of...