Detalhe da pesquisa
1.
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson's disease and multiple system atrophy?
Acta Neuropathol
; 125(5): 753-69, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23404372
2.
Insulin and IGF-1 signalling: longevity, protein homoeostasis and Alzheimer's disease.
Biochem Soc Trans
; 40(4): 721-7, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22817723
3.
Cerebral mitochondrial electron transport chain dysfunction in multiple system atrophy and Parkinson's disease.
Sci Rep
; 9(1): 6559, 2019 04 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-31024027
4.
Immunohistochemical and Molecular Investigations Show Alteration in the Inflammatory Profile of Multiple System Atrophy Brain.
J Neuropathol Exp Neurol
; 77(7): 598-607, 2018 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29850876
5.
Coenzyme Q10 Levels Are Decreased in the Cerebellum of Multiple-System Atrophy Patients.
PLoS One
; 11(2): e0149557, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26894433
6.
Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation.
Mol Neurodegener
; 10: 41, 2015 Aug 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-26306801
7.
A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations.
JAMA Neurol
; 71(9): 1162-71, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25003242