Detalhe da pesquisa
1.
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia.
Am J Hum Genet
; 2024 Jun 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38889728
2.
Somatic comorbidities and Alzheimer's disease treatment.
Neurol Sci
; 34(9): 1581-9, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23370896
3.
A Comparison of Behavioral and Psychological Symptoms of Dementia (BPSD) and BPSD Sub-Syndromes in Early-Onset and Late-Onset Alzheimer's Disease.
J Alzheimers Dis
; 85(2): 691-699, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34864668
4.
Neuropsychiatric or Behavioral and Psychological Symptoms of Dementia (BPSD): Focus on Prevalence and Natural History in Alzheimer's Disease and Frontotemporal Dementia.
Front Neurol
; 13: 832199, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35812082
5.
MAPT V363I variation in a sporadic case of frontotemporal dementia: variable penetrant mutation or rare polymorphism?
Alzheimer Dis Assoc Disord
; 25(1): 96-9, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21343707
6.
A Novel Mutation (D395A) in Valosin-Containing Protein Gene Is Associated With Early Onset Frontotemporal Dementia in an Italian Family.
Front Genet
; 12: 795029, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34917136
7.
Amyloid Precursor Protein A713T Mutation in Calabrian Patients with Alzheimer's Disease: A Population Genomics Approach to Estimate Inheritance from a Common Ancestor.
Biomedicines
; 10(1)2021 Dec 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35052700
8.
Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia.
Neurol Sci
; 31(1): 65-70, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19768372
9.
C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts.
Neurology
; 95(24): e3288-e3302, 2020 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32943482
10.
Uncoupling protein 4 (UCP4) gene variability in neurodegenerative disorders: further evidence of association in Frontotemporal dementia.
Aging (Albany NY)
; 10(11): 3283-3293, 2018 11 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30425186
11.
Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia.
J Alzheimers Dis
; 61(3): 1179-1187, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29332048
12.
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
em Inglês
| MEDLINE | ID: mdl-29724592
13.
Role of Niemann-Pick Type C Disease Mutations in Dementia.
J Alzheimers Dis
; 55(3): 1249-1259, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-27792009
14.
The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family.
Neurobiol Aging
; 56: 213.e7-213.e12, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28532646
15.
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family.
Neurology
; 84(22): 2266-73, 2015 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25948718
16.
Identification of three novel LRRK2 mutations associated with Parkinson's disease in a Calabrian population.
J Alzheimers Dis
; 38(2): 351-7, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-23963289
17.
Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome.
Neurobiol Aging
; 35(11): 2657.e7-2657.e11, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25022973
18.
Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism.
J Neurol
; 255(4): 604-6, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18350357
19.
Role of TOMM40 rs10524523 polymorphism in onset of alzheimer's disease caused by the PSEN1 M146L mutation.
J Alzheimers Dis
; 37(2): 285-9, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23792692
20.
Presenilin 2 Ser130Leu mutation in a case of late-onset "sporadic" Alzheimer's disease.
J Neurol
; 254(3): 391-3, 2007 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-17345043