Changes in endolysosomal enzyme activities in cerebrospinal fluid of patients with Parkinson's disease
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Title
Changes in endolysosomal enzyme activities in cerebrospinal fluid of patients with Parkinson's disease
Authors
Keywords
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Journal
MOVEMENT DISORDERS
Volume 28, Issue 6, Pages 747-754
Publisher
Wiley
Online
2013-05-28
DOI
10.1002/mds.25495
References
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Note: Only part of the references are listed.- Glucocerebrosidase deficiency in substantia nigra of parkinson disease brains
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- Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration
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- GM1 ganglioside in Parkinson's disease: Results of a five year open study
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- Prion-like transmission of protein aggregates in neurodegenerative diseases
- (2010) Patrik Brundin et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
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- Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease
- (2009) Juliane Neumann et al. BRAIN
- Cerebrospinal fluid β-glucocerebrosidase activity is reduced in Dementia with Lewy Bodies
- (2009) L. Parnetti et al. NEUROBIOLOGY OF DISEASE
- Alterations in lysosomal and proteasomal markers in Parkinson's disease: Relationship to alpha-synuclein inclusions
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- Cathepsin D Is the Main Lysosomal Enzyme Involved in the Degradation of α-Synuclein and Generation of Its Carboxy-Terminally Truncated Species†
- (2008) Daniel Sevlever et al. BIOCHEMISTRY
- The role of autophagy-lysosome pathway in neurodegeneration associated with Parkinson's disease
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- Assembly-dependent endocytosis and clearance of extracellular a-synuclein
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- Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
- (2008) Daniel G Healy et al. LANCET NEUROLOGY
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