Detalhe da pesquisa
1.
Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.
Acta Neuropathol
; 139(5): 959-962, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31955222
2.
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.
Acta Neuropathol
; 138(2): 237-250, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31131421
3.
Longitudinal Neuropsychological Study of Presymptomatic c.709-1G>A Progranulin Mutation Carriers.
J Int Neuropsychol Soc
; 25(1): 39-47, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30369339
4.
Neuropsychological features of asymptomatic c.709-1G>A progranulin mutation carriers.
J Int Neuropsychol Soc
; 18(6): 1086-90, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23158232
5.
Does culture shape our understanding of others' thoughts and emotions? An investigation across 12 countries.
Neuropsychology
; 36(7): 664-682, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-35834208
6.
Prion protein codon 129 polymorphism modifies age at onset of frontotemporal dementia with the C.709-1G>A progranulin mutation.
Alzheimer Dis Assoc Disord
; 25(1): 93-5, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-20711061
7.
Blood Markers in Healthy-Aged Nonagenarians: A Combination of High Telomere Length and Low Amyloidß Are Strongly Associated With Healthy Aging in the Oldest Old.
Front Aging Neurosci
; 10: 380, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30546303
8.
The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics.
PLoS One
; 12(6): e0178093, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28594853
9.
MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEÉ4 Noncarriers: Results from the Dementia Genetics Spanish Consortium.
J Alzheimers Dis
; 49(2): 343-52, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26444794
10.
Identification of a novel THAP1 mutation at R29 amino-acid residue in sporadic patients with early-onset dystonia.
Mov Disord
; 24(16): 2428-9, 2009 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19908320
11.
Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes.
Neurobiol Aging
; 35(11): 2657.e13-2657.e19, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25042114
12.
Distinctive age-related temporal cortical thinning in asymptomatic granulin gene mutation carriers.
Neurobiol Aging
; 34(5): 1462-8, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23218900
13.
A novel PRNP Y218N mutation in Gerstmann-Sträussler-Scheinker disease with neurofibrillary degeneration.
J Neuropathol Exp Neurol
; 69(8): 789-800, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20613639
14.
Mutations in progranulin gene: clinical, pathological, and ribonucleic acid expression findings.
Biol Psychiatry
; 63(10): 946-52, 2008 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17950702
15.
Levodopa-induced ocular dyskinesias in Parkinson's disease.
Mov Disord
; 17(1): 186-7, 2002 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-11835460
16.
Possible sporadic rapid-onset dystonia-parkinsonism.
Mov Disord
; 17(3): 608-9, 2002 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-12112218
17.
A common haplotype associated with the Basque 2362AG --> TCATCT mutation in the muscular calpain-3 gene.
Hum Biol
; 76(5): 731-41, 2004 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-15757244