Grisel Lopez
Overview
Explore the profile of Grisel Lopez including associated specialties, affiliations and a list of published articles.
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53
Citations
2532
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Recent Articles
11.
Gleason A, Tayebi N, Lopez G, Sidransky E
Mov Disord
. 2022 Jan;
37(3):653.
PMID: 35075696
No abstract available.
12.
Eisenberg D, Lopez G, Gregory M, Berman K, Sidransky E
Mov Disord
. 2021 Nov;
37(3):629-634.
PMID: 34762337
Background: Mutations in GBA1 are a common genetic risk factor for parkinsonism; however, penetrance is incomplete, and biomarkers of future progression to parkinsonism are needed. Both nigral sonography and striatal...
13.
Isonaka R, Goldstein D, Zhu W, Yoon E, Ehrlich D, Schindler A, et al.
Mov Disord
. 2021 Jun;
36(10):2346-2357.
PMID: 34076298
Background: Cytoplasmic inclusions of α-synuclein (α-syn) in brainstem neurons are characteristic of idiopathic Parkinson's disease (PD). PD also entails α-syn buildup in sympathetic nerves. Among genetic forms of PD, the...
14.
Chia R, Sabir M, Bandres-Ciga S, Saez-Atienzar S, Reynolds R, Gustavsson E, et al.
Nat Genet
. 2021 Feb;
53(3):294-303.
PMID: 33589841
The genetic basis of Lewy body dementia (LBD) is not well understood. Here, we performed whole-genome sequencing in large cohorts of LBD cases and neurologically healthy controls to study the...
15.
Ryan E, Nguyen M, Lopez G, Mitchell K, Lowery M, Singh S, et al.
Am J Med
. 2020 Dec;
134(6):745-748.
PMID: 33359772
No abstract available.
16.
Poffenberger C, Inati S, Tayebi N, Stubblefield B, Ryan E, Schiffmann R, et al.
Mol Genet Metab
. 2020 Nov;
131(3):358-363.
PMID: 33183916
The clinical phenotype of Gaucher disease type 3 (GD3), a neuronopathic lysosomal storage disorder, encompasses a wide array of neurological manifestations including neuro-ophthalmological findings, developmental delay, and seizures including progressive...
17.
Ryan E, Amato D, MacKenzie J, Sidransky E, Lopez G
Mov Disord Clin Pract
. 2020 Oct;
7(7):834-837.
PMID: 33043079
Background: The link between Parkinson's disease (PD), the second most common neurodegenerative disorder, and nonneuronopathic Gaucher disease (GD) is well established. Currently, PD is primarily associated with nonneuronopathic GD; however,...
18.
Tayebi N, Lopez G, Do J, Sidransky E
Trends Mol Med
. 2020 Sep;
26(10):913-923.
PMID: 32948448
Mutations in GBA1, the gene encoding the lysosomal hydrolase glucocerebrosidase (GCase), are a risk factor for parkinsonism. Pursuing the potential mechanisms underlying this risk in aging neurons, we propose a...
19.
Roshan Lal T, Seehra G, Steward A, Poffenberger C, Ryan E, Tayebi N, et al.
Neurology
. 2020 Aug;
95(15):e2119-e2130.
PMID: 32764102
Objective: To gather natural history data to better understand the changing course of type 2 Gaucher disease (GD2) in order to guide future interventional protocols. Methods: A structured interview was...
20.
Mistry P, Balwani M, Barbouth D, Burrow T, Ginns E, Goker-Alpan O, et al.
Mol Genet Metab
. 2020 May;
130(3):164-169.
PMID: 32471800
No abstract available.