Detalhe da pesquisa
1.
Homozygous CADPS2 Mutations Cause Neurodegenerative Disease with Lewy Body-like Pathology in Parrots.
Mov Disord
; 37(12): 2345-2354, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36086934
2.
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease.
Nature
; 505(7484): 550-554, 2014 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-24336208
3.
Multiple system atrophy and apolipoprotein E.
Mov Disord
; 33(4): 647-650, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29442376
4.
Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor.
Hum Mol Genet
; 24(20): 5677-86, 2015 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26188006
5.
(Patho-)physiological relevance of PINK1-dependent ubiquitin phosphorylation.
EMBO Rep
; 16(9): 1114-30, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26162776
6.
Genome-wide association study in essential tremor identifies three new loci.
Brain
; 139(Pt 12): 3163-3169, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27797806
7.
Epigenetic regulation in Parkinson's disease.
Acta Neuropathol
; 132(4): 515-30, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27358065
8.
MAPT haplotype H1G is associated with increased risk of dementia with Lewy bodies.
Alzheimers Dement
; 12(12): 1297-1304, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27287057
9.
Automated neuromelanin imaging as a diagnostic biomarker for Parkinson's disease.
Mov Disord
; 30(7): 945-52, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25772492
10.
No association of the SLC1A2 rs3794087 allele with risk for essential tremor in the Spanish population.
Pharmacogenet Genomics
; 23(11): 587-90, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23949322
11.
LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis.
BMC Neurol
; 13: 34, 2013 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-23574883
12.
Rare variants in MC1R/TUBB3 exon 1 are not associated with Parkinson's disease.
Ann Neurol
; 79(2): 331, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26677074
13.
LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation.
Mov Disord
; 27(1): 146-51, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22038903
14.
Common variation in the LRRK2 gene is a risk factor for Parkinson's disease.
Mov Disord
; 27(14): 1822-5, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23115130
15.
Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis.
JAMA Neurol
; 79(2): 185-193, 2022 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34982113
16.
Gamma-aminobutyric acid GABRA4, GABRE, and GABRQ receptor polymorphisms and risk for essential tremor.
Pharmacogenet Genomics
; 21(7): 436-9, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21422964
17.
A polymorphism located at an ATG transcription start site of the heme oxygenase-2 gene is associated with classical Parkinson's disease.
Pharmacogenet Genomics
; 21(9): 565-71, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21709601
18.
LINGO1 gene analysis in Parkinson's disease phenotypes.
Mov Disord
; 26(4): 722-7, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21506150
19.
Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's disease.
Mov Disord
; 26(5): 819-23, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21425343
20.
PINK1-linked parkinsonism is associated with Lewy body pathology.
Brain
; 133(Pt 4): 1128-42, 2010 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-20356854