Detalhe da pesquisa
1.
Effect of Functional BDNF and COMT Polymorphisms on Symptoms and Regional Brain Volume in Frontotemporal Dementia and Corticobasal Syndrome.
J Neuropsychiatry Clin Neurosci
; 32(4): 362-369, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32397876
2.
Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies.
PLoS Med
; 15(1): e1002487, 2018 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29315334
3.
Correction: Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies.
PLoS Med
; 15(1): e1002504, 2018 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29377952
4.
Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia.
Acta Neuropathol
; 133(5): 825-837, 2017 05.
Artigo
Inglês
| MEDLINE | ID: mdl-28271184
5.
Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases.
J Neurol Neurosurg Psychiatry
; 88(2): 152-164, 2017 02.
Artigo
Inglês
| MEDLINE | ID: mdl-27899424
6.
A repository based on a dynamically extensible data model supporting multidisciplinary research in neuroscience.
BMC Med Inform Decis Mak
; 12: 115, 2012 Oct 08.
Artigo
Inglês
| MEDLINE | ID: mdl-23043673
7.
Pathological correlates of frontotemporal lobar degeneration in the elderly.
Acta Neuropathol
; 121(3): 365-71, 2011 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-20978901
8.
The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene.
Acta Neuropathol
; 122(1): 99-110, 2011 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-21424531
9.
Novel missense mutation in charged multivesicular body protein 2B in a patient with frontotemporal dementia.
Alzheimer Dis Assoc Disord
; 24(4): 397-401, 2010.
Artigo
Inglês
| MEDLINE | ID: mdl-20592581
10.
Progranulin (GRN) in two siblings of a Latino family and in other patients with schizophrenia.
Neurocase
; 16(3): 273-9, 2010 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-20087814
11.
Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.
Mov Disord
; 24(5): 662-6, 2009 Apr 15.
Artigo
Inglês
| MEDLINE | ID: mdl-19205068
12.
Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia.
Sci Rep
; 9(1): 10854, 2019 07 26.
Artigo
Inglês
| MEDLINE | ID: mdl-31350420
13.
Novel GCH1 mutation in a Brazilian family with dopa-responsive dystonia.
Mov Disord
; 23(2): 299-302, 2008 Jan 30.
Artigo
Inglês
| MEDLINE | ID: mdl-18044725
14.
Protein network analysis reveals selectively vulnerable regions and biological processes in FTD.
Neurol Genet
; 4(5): e266, 2018 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-30283816
15.
CXCR4 involvement in neurodegenerative diseases.
Transl Psychiatry
; 8(1): 73, 2018 04 11.
Artigo
Inglês
| MEDLINE | ID: mdl-29636460
16.
Selective Genetic Overlap Between Amyotrophic Lateral Sclerosis and Diseases of the Frontotemporal Dementia Spectrum.
JAMA Neurol
; 75(7): 860-875, 2018 07 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29630712
17.
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.
Lancet Neurol
; 17(6): 548-558, 2018 06.
Artigo
Inglês
| MEDLINE | ID: mdl-29724592
18.
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
Lancet Neurol
; 6(10): 857-68, 2007 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-17826340
19.
Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.
Brain
; 129(Pt 11): 3115-23, 2006 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-17030534
20.
Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.
J Alzheimers Dis
; 56(4): 1271-1278, 2017.
Artigo
Inglês
| MEDLINE | ID: mdl-28128768