Detalhe da pesquisa
1.
Assessing the relationship between monoallelic PRKN mutations and Parkinson's risk.
Hum Mol Genet
; 30(1): 78-86, 2021 03 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-33448283
2.
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study.
Brain
; 142(9): 2828-2844, 2019 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31324919
3.
Ambroxol for the Treatment of Patients With Parkinson Disease With and Without Glucocerebrosidase Gene Mutations: A Nonrandomized, Noncontrolled Trial.
JAMA Neurol
; 77(4): 427-434, 2020 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31930374
4.
Analysis of the genetic variability in Parkinson's disease from Southern Spain.
Neurobiol Aging
; 37: 210.e1-210.e5, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26518746
5.
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies.
Neurology
; 82(4): 292-9, 2014 01 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-24363131
6.
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