Detalhe da pesquisa
1.
Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 mice.
J Neurol Neurosurg Psychiatry
; 91(2): 162-171, 2020 02.
Artigo
Inglês
| MEDLINE | ID: mdl-31690696
2.
TDP-43 proteinopathies: pathological identification of brain regions differentiating clinical phenotypes.
Brain
; 138(Pt 10): 3110-22, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-26231953
3.
Genetics of dementia.
Lancet
; 383(9919): 828-40, 2014 Mar 01.
Artigo
Inglês
| MEDLINE | ID: mdl-23927914
4.
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions.
Acta Neuropathol
; 127(3): 407-18, 2014 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-24442578
5.
DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E in vitro.
Mov Disord
; 29(13): 1606-14, 2014 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-24375821
6.
Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: genetic, clinical and neuropathological analysis.
Acta Neuropathol
; 125(4): 523-33, 2013 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-23338750
7.
Srp20 regulates TrkB pre-mRNA splicing to generate TrkB-Shc transcripts with implications for Alzheimer's disease.
J Neurochem
; 123(1): 159-71, 2012 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-22788679
8.
Leucine-rich repeat kinase 2 and alternative splicing in Parkinson's disease.
Mov Disord
; 27(8): 1004-11, 2012 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-22528366
9.
Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron disease.
Ann Neurol
; 68(5): 639-49, 2010 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-21031579
10.
Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?
Brain
; 138(Pt 10): e385, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-25953780
11.
Glycogen synthase kinase-3beta and tau genes interact in Alzheimer's disease.
Ann Neurol
; 64(4): 446-54, 2008 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-18991351
12.
The underacknowledged PPA-ALS: A unique clinicopathologic subtype with strong heritability.
Neurology
; 92(12): e1354-e1366, 2019 03 19.
Artigo
Inglês
| MEDLINE | ID: mdl-30770429
13.
Variable phenotype of Alzheimer's disease with spastic paraparesis.
J Neurochem
; 104(3): 573-83, 2008 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-17995932
14.
Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.
BMC Neurol
; 8: 32, 2008 Aug 29.
Artigo
Inglês
| MEDLINE | ID: mdl-18755042
15.
Effect of Fluvoxamine on Amyloid-ß Peptide Generation and Memory.
J Alzheimers Dis
; 62(4): 1777-1787, 2018.
Artigo
Inglês
| MEDLINE | ID: mdl-29614681
16.
No association of spastic paraparesis genes in PSEN1 Alzheimer's disease with spastic paraparesis.
Neuroreport
; 18(12): 1267-9, 2007 Aug 06.
Artigo
Inglês
| MEDLINE | ID: mdl-17632280
17.
Mutations in progranulin explain atypical phenotypes with variants in MAPT.
Brain
; 129(Pt 11): 3124-6, 2006 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-17071927
18.
Finding MAPT Mutations in Frontotemporal Dementia and Other Tauopathies.
Methods Mol Biol
; 1523: 307-324, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-27975259
19.
Assessment of amyloid ß in pathologically confirmed frontotemporal dementia syndromes.
Alzheimers Dement (Amst)
; 9: 10-20, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28653036
20.
Role of the Long Non-Coding RNA MAPT-AS1 in Regulation of Microtubule Associated Protein Tau (MAPT) Expression in Parkinson's Disease.
PLoS One
; 11(6): e0157924, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-27336847