Detalhe da pesquisa
1.
Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons.
Am J Hum Genet
; 103(6): 874-892, 2018 12 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30503521
2.
Association of MAPT H1 subhaplotypes with neuropathology of lewy body disease.
Mov Disord
; 34(9): 1325-1332, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31234228
3.
Multiple system atrophy and apolipoprotein E.
Mov Disord
; 33(4): 647-650, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29442376
4.
Association of ABI3 and PLCG2 missense variants with disease risk and neuropathology in Lewy body disease and progressive supranuclear palsy.
Acta Neuropathol Commun
; 8(1): 172, 2020 10 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-33092647
5.
ATP13A2 variability in Parkinson disease.
Hum Mutat
; 30(3): 406-10, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19085912
6.
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease.
Ann Neurol
; 64(1): 88-92, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18412265
7.
FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expression.
Mov Disord
; 24(3): 455-9, 2009 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19133659
8.
Association of MAPT Subhaplotypes With Risk of Progressive Supranuclear Palsy and Severity of Tau Pathology.
JAMA Neurol
; 76(6): 710-717, 2019 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30882841
9.
X-Linked Lymphoproliferative Syndrome Presenting as Adult-Onset Multi-Infarct Dementia.
J Neuropathol Exp Neurol
; 78(5): 460-466, 2019 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30990878
10.
Genetic variation of Omi/HtrA2 and Parkinson's disease.
Parkinsonism Relat Disord
; 14(7): 539-43, 2008 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-18790661
11.
Dopamine beta-hydroxylase -1021C>T association and Parkinson's disease.
Parkinsonism Relat Disord
; 14(7): 544-7, 2008 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-18722802
12.
PCNT point mutations and familial intracranial aneurysms.
Neurology
; 91(23): e2170-e2181, 2018 12 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30413633
13.
APOE ε4 is associated with severity of Lewy body pathology independent of Alzheimer pathology.
Neurology
; 91(12): e1182-e1195, 2018 09 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-30143564
14.
Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variants.
Neurobiol Aging
; 66: 177.e7-177.e10, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29398119
15.
ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African Americans.
Mol Neurodegener
; 13(1): 53, 2018 10 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30326945
16.
Association study between multiple system atrophy and TREM2 p.R47H.
Neurol Genet
; 4(4): e257, 2018 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-30109269
17.
Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease.
Autophagy
; 14(8): 1404-1418, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29947276
18.
Reported mutations in GIGYF2 are not a common cause of Parkinson's disease.
Mov Disord
; 24(4): 619-20, 2009 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19133664
19.
DCTN1 variation in pathologically-confirmed PSP and CBD tauopathy.
Parkinsonism Relat Disord
; 44: 151-153, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28867162