Detalhe da pesquisa
1.
Unravelling the immune signature of herpes zoster: Insights into pathophysiology and the HLA risk profile.
J Infect Dis
; 2024 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38195164
2.
Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability.
Acta Neuropathol
; 137(6): 901-918, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30874922
3.
Clinical features of TBK1 carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort.
Brain
; 139(Pt 2): 452-67, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26674655
4.
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.
Acta Neuropathol
; 128(3): 397-410, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24899140
5.
Lack of functional TCR-epitope interaction is associated with herpes zoster through reduced downstream T cell activation.
Cell Rep
; 43(4): 114062, 2024 Apr 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38588339
6.
Guanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia.
Mov Disord
; 27(11): 1451-6, 2012 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22976901
7.
TMEM106B is associated with frontotemporal lobar degeneration in a clinically diagnosed patient cohort.
Brain
; 134(Pt 3): 808-15, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21354975
8.
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21.
Nature
; 442(7105): 920-4, 2006 Aug 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-16862115
9.
CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro.
Hum Mol Genet
; 17(2): 313-22, 2008 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17956895
10.
Serum biomarker for progranulin-associated frontotemporal lobar degeneration.
Ann Neurol
; 65(5): 603-9, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19288468
11.
Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease.
Hum Mutat
; 29(6): 832-40, 2008 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-18401856
12.
Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients.
Eur J Hum Genet
; 16(4): 471-9, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18197194
13.
A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder.
Brain
; 130(Pt 9): 2277-91, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17681982
14.
Clinical variability and onset age modifiers in an extended Belgian GRN founder family.
Neurobiol Aging
; 67: 84-94, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29653316
15.
Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia.
Neurobiol Aging
; 66: 181.e3-181.e10, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29555433
16.
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia.
Hum Mutat
; 28(4): 416, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17345602
17.
Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family.
Arch Neurol
; 64(10): 1436-46, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17923627
18.
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.
Brain
; 129(Pt 4): 841-52, 2006 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-16495329
19.
Clinical Evidence of Disease Anticipation in Families Segregating a C9orf72 Repeat Expansion.
JAMA Neurol
; 74(4): 445-452, 2017 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28192553
20.
Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson's disease and increase susceptibility to dementia in a Flanders-Belgian cohort.
Neurosci Lett
; 629: 160-164, 2016 08 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-27397011