Glucocerebrosidase involvement in Parkinson Disease and other Synucleinopathies
Mutations in the both copies (homozygous or compound heterozygous) of the gene encoding the lysosomal enzyme glucocerebrosidase, which cleaves the glycolipid glucocerebroside into glucose and ceramide causes Gaucher Disease. However, multiple independent studies have also reported an association bet...
Main Author: | Maria Rosario Almeida |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2012-04-01
|
Series: | Frontiers in Neurology |
Subjects: | |
Online Access: | http://journal.frontiersin.org/Journal/10.3389/fneur.2012.00065/full |
Similar Items
-
Glucocerebrosidase Defects as a Major Risk Factor for Parkinson’s Disease
by: Micol Avenali, et al.
Published: (2020-04-01) -
The Role of Neutral Sphingolipids in the Pathogenesis of Parkinson Disease and Dementia with Lewy Bodies
by: Singh, Priyanka
Published: (2013) -
The Role of Neutral Sphingolipids in the Pathogenesis of Parkinson Disease and Dementia with Lewy Bodies
by: Singh, Priyanka
Published: (2013) -
Dementia with Lewy bodies and Parkinson’s disease dementia-two independent disorders or one clinical entity within a clinical spectrum of synucleinopathies?
by: Papuć Ewa
Published: (2020-09-01) -
Novel antibodies detect additional α-synuclein pathology in synucleinopathies: potential development for immunotherapy
by: Jacqui T. Nimmo, et al.
Published: (2020-11-01)