Given the clear role of GBA in the pathogenesis of Parkinson's disease (PD) and its impact on phenotypical characteristics, this review provides an overview of the current knowledge of GBA-associated PD with a special focus on clinical trajectories and the underlying pathological mechanisms. Importantly, differences and characteristics based on mutation severity are recognized, and current as well as potential future treatment options are discussed. These findings will inform future strategies for patient stratification and cohort enrichment as well as suitable outcome measures when designing clinical trials
The discovery of genes involved in familial as well as sporadic forms of Parkinson disease (PD) cons...
INTRODUCTION: Variants in the GBA1 gene have been identified as a common risk factor for Parkinson's...
In recent years, numerous clinical trials for disease modification in Parkinson’s disease (PD) have ...
peer reviewedGiven the clear role of GBA in the pathogenesis of Parkinson's disease (PD) and its imp...
Since its first description in the XIV century, the understanding of Parkinson disease (PD) has adv...
The following comprises a short summary of this clinical observation study including the objective, ...
Background: Parkinson’s disease (PD) is a common neurodegenerative disorder mainly characterized by ...
The GBA gene encodes for the lysosomal enzyme glucocerebrosidase (GCase), which maintains glycosphin...
Objective To establish the significance of glucocerebrosidase gene (GBA) carrier status on motor i...
Objectives To examine the influence of the glucocerebrosidase (GBA) mutation carrier state on age at...
Parkinson’s disease (PD) and Lewy Body Dementias (LBD) are two distinct synucleinopathies with a gre...
Objectives: To examine the influence of the glucocerebrosidase (GBA) mutation carrier state on age a...
Dysfunction of the endolysosomal system is implicated in the pathogenesis of both sporadic and famil...
OBJECTIVES: GBA1 mutations are a frequent risk factor for Parkinson disease (PD). The aim of this st...
In recent years, a precision medicine approach, which customizes medical treatments based on patient...
The discovery of genes involved in familial as well as sporadic forms of Parkinson disease (PD) cons...
INTRODUCTION: Variants in the GBA1 gene have been identified as a common risk factor for Parkinson's...
In recent years, numerous clinical trials for disease modification in Parkinson’s disease (PD) have ...
peer reviewedGiven the clear role of GBA in the pathogenesis of Parkinson's disease (PD) and its imp...
Since its first description in the XIV century, the understanding of Parkinson disease (PD) has adv...
The following comprises a short summary of this clinical observation study including the objective, ...
Background: Parkinson’s disease (PD) is a common neurodegenerative disorder mainly characterized by ...
The GBA gene encodes for the lysosomal enzyme glucocerebrosidase (GCase), which maintains glycosphin...
Objective To establish the significance of glucocerebrosidase gene (GBA) carrier status on motor i...
Objectives To examine the influence of the glucocerebrosidase (GBA) mutation carrier state on age at...
Parkinson’s disease (PD) and Lewy Body Dementias (LBD) are two distinct synucleinopathies with a gre...
Objectives: To examine the influence of the glucocerebrosidase (GBA) mutation carrier state on age a...
Dysfunction of the endolysosomal system is implicated in the pathogenesis of both sporadic and famil...
OBJECTIVES: GBA1 mutations are a frequent risk factor for Parkinson disease (PD). The aim of this st...
In recent years, a precision medicine approach, which customizes medical treatments based on patient...
The discovery of genes involved in familial as well as sporadic forms of Parkinson disease (PD) cons...
INTRODUCTION: Variants in the GBA1 gene have been identified as a common risk factor for Parkinson's...
In recent years, numerous clinical trials for disease modification in Parkinson’s disease (PD) have ...