Detalhe da pesquisa
1.
Differences in the Presentation and Progression of Parkinson's Disease by Sex.
Mov Disord
; 36(1): 106-117, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33002231
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.
Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients.
Proc Natl Acad Sci U S A
; 107(27): 12335-8, 2010 Jul 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-20566859
4.
Mutational Analysis of Known ALS Genes in an Italian Population-Based Cohort.
Neurology
; 96(4): e600-e609, 2021 01 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-33208543
5.
Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis.
Sci Rep
; 9(1): 18865, 2019 12 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31827228
6.
Genetic risk factors in Finnish patients with Parkinson's disease.
Parkinsonism Relat Disord
; 45: 39-43, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-29029963
7.
A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern Italy.
J Alzheimers Dis
; 53(2): 475-85, 2016 05 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-27258413
8.
Influence of Coding Variability in APP-Aß Metabolism Genes in Sporadic Alzheimer's Disease.
PLoS One
; 11(6): e0150079, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27249223
9.
Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease.
Neurobiol Aging
; 35(12): 2881.e1-2881.e6, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25104557
10.
Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease.
Neurobiol Aging
; 35(10): 2422.e13-6, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24880964