Frequency of Hereditary and GBA1‐Related Parkinsonism in Latin America: A Systematic Review and Meta‐Analysis
P Saffie Awad, D Teixeira‐dos‐Santos… - Movement …, 2024 - Wiley Online Library
Background Identifying hereditary parkinsonism is valuable for diagnosis, genetic
counseling, patient prioritization in trials, and studying the disease for personalized …
counseling, patient prioritization in trials, and studying the disease for personalized …
[HTML][HTML] Phenotypic effect of GBA1 variants in individuals with and without Parkinson's disease: The RAPSODI study
M Toffoli, H Chohan, S Mullin, A Jesuthasan… - Neurobiology of …, 2023 - Elsevier
Background Variants in the GBA1 gene cause the lysosomal storage disorder Gaucher
disease (GD). They are also risk factors for Parkinson's disease (PD), and modify the …
disease (GD). They are also risk factors for Parkinson's disease (PD), and modify the …
Predictors of the Rapid Progression in Prodromal Parkinson's Disease: A Longitudinal Follow-Up Study
P Liu, L Chen, X He, L Mao - Gerontology, 2024 - karger.com
Introduction: Parkinson's disease (PD) is characterized by a prodromal phase preceding the
onset of classic motor symptoms. The duration and clinical manifestations of prodromal PD …
onset of classic motor symptoms. The duration and clinical manifestations of prodromal PD …
Evolution of Clinical, Biochemical and Microbiome Biomarkers of Conversion to Parkinson Disease in Glucocerebrosidase Mutation Carriers: Insights into Aetiology …
E Menozzi - 2024 - discovery.ucl.ac.uk
The penetrance of heterozygous variants in GBA1, the commonest genetic risk factor for
Parkinson disease (PD), is incomplete (10%-30%), but the reasons underlying this …
Parkinson disease (PD), is incomplete (10%-30%), but the reasons underlying this …