Emerging neuroimaging biomarkers across disease stage in Parkinson disease: a review

T Mitchell, S Lehéricy, SY Chiu, AP Strafella… - JAMA …, 2021 - jamanetwork.com
Importance Imaging biomarkers in Parkinson disease (PD) are increasingly important for
monitoring progression in clinical trials and also have the potential to improve clinical care …

Linking the cerebellum to Parkinson disease: an update

T Li, W Le, J Jankovic - Nature Reviews Neurology, 2023 - nature.com
Parkinson disease (PD) is characterized by heterogeneous motor and non-motor symptoms,
resulting from neurodegeneration involving various parts of the central nervous system …

Functional brain networks in the evaluation of patients with neurodegenerative disorders

M Perovnik, T Rus, KA Schindlbeck… - Nature Reviews …, 2023 - nature.com
Network analytical tools are increasingly being applied to brain imaging maps of resting
metabolic activity (PET) or blood oxygenation-dependent signals (functional MRI) to …

Glucocerebrosidase mutations and Parkinson disease

SRL Vieira, AHV Schapira - Journal of Neural Transmission, 2022 - Springer
The discovery of glucocerebrosidase (GBA1) mutations as the greatest numerical genetic
risk factor for the development of Parkinson disease (PD) resulted in a paradigm shift within …

Exploring the Genotype–Phenotype Correlation in GBA-Parkinson Disease: Clinical Aspects, Biomarkers, and Potential Modifiers

E Menozzi, AHV Schapira - Frontiers in Neurology, 2021 - frontiersin.org
Variants in the glucocerebrosidase (GBA) gene are the most common genetic risk factor for
Parkinson disease (PD). These include pathogenic variants causing Gaucher disease …

GBA Variants in Parkinson's Disease: Clinical, Metabolomic, and Multimodal Neuroimaging Phenotypes

A Greuel, JP Trezzi, E Glaab, MC Ruppert… - Movement …, 2020 - Wiley Online Library
Background Alterations in the GBA gene (NM_000157. 3) are the most important genetic risk
factor for Parkinson's disease (PD). Biallelic GBA mutations cause the lysosomal storage …

GBA1 Gene Mutations in α-Synucleinopathies—Molecular Mechanisms Underlying Pathology and Their Clinical Significance

Z Granek, J Barczuk, N Siwecka… - International Journal of …, 2023 - mdpi.com
α-Synucleinopathies comprise a group of neurodegenerative diseases characterized by
altered accumulation of a protein called α-synuclein inside neurons and glial cells. This …

A network imaging biomarker of X‐linked dystonia‐parkinsonism

M Niethammer, CC Tang, RDG Jamora… - Annals of …, 2023 - Wiley Online Library
Objective The purpose of this study was to characterize a metabolic brain network
associated with X‐linked dystonia‐parkinsonism (XDP). Methods Thirty right‐handed …

Neuroimaging in glucocerebrosidase‐associated Parkinsonism: A systematic review

M Filippi, R Balestrino, S Basaia… - Movement Disorders, 2022 - Wiley Online Library
Background Mutations in the GBA gene cause Gaucher's disease (GD) and constitute the
most frequent genetic risk factor for idiopathic Parkinson's disease (iPD). Nonmanifesting …

Molecular Imaging in Parkinsonian Disorders—What's New and Hot?

S Prange, H Theis, M Banwinkler, T van Eimeren - Brain Sciences, 2022 - mdpi.com
Highlights Imaging of the dopamine transporter (DAT)(in particular using 11C-or 18F-PE2I)
most reliably and precisely measures neurodegeneration of the dopaminergic system in …