Detalhe da pesquisa
1.
A novel bio-inspired strategy to prevent amyloidogenesis and synaptic damage in Alzheimer's disease.
Mol Psychiatry
; 27(12): 5227-5234, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36028569
2.
MAPT Q336H mutation: Intrafamilial phenotypic heterogeneity in a new Italian family.
Eur J Neurol
; 29(5): 1529-1533, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35020237
3.
SORL1 gene mutation and octapeptide repeat insertion in PRNP gene in a case presenting with rapidly progressive dementia and cerebral amyloid angiopathy.
Eur J Neurol
; 29(11): 3139-3146, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35789031
4.
Neurosyphilis Mimicking Behavioral Variant of Frontotemporal Dementia in a 59-Year-Old Man.
Cogn Behav Neurol
; 35(2): 140-146, 2022 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35639012
5.
Pathological 25 kDa C-Terminal Fragments of TDP-43 Are Present in Lymphoblastoid Cell Lines and Extracellular Vesicles from Patients Affected by Frontotemporal Lobar Degeneration and Neuronal Ceroidolipofuscinosis Carrying a GRN Mutation.
Int J Mol Sci
; 23(22)2022 Nov 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36430231
6.
The PINK1 p.Asn521Thr Variant Is Associated with Earlier Disease Onset in GRN/C9orf72 Frontotemporal Lobar Degeneration.
Int J Mol Sci
; 23(21)2022 Oct 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36361641
7.
Singular cases of Alzheimer's disease disclose new and old genetic "acquaintances".
Neurol Sci
; 42(5): 2021-2029, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-33006056
8.
Microglial Heterogeneity and Its Potential Role in Driving Phenotypic Diversity of Alzheimer's Disease.
Int J Mol Sci
; 22(5)2021 Mar 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33803478
9.
Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA): the SENECA project.
Neurol Sci
; 41(8): 2193-2200, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32166471
10.
Understanding the Pathophysiology of Cerebral Amyloid Angiopathy.
Int J Mol Sci
; 21(10)2020 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-32414028
11.
Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges.
Ann Neurol
; 84(3): 347-360, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30048013
12.
Neuro-Behçet's disease presenting as an isolated progressive cognitive and behavioral syndrome.
Neurocase
; 24(5-6): 238-241, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30583716
13.
Towards an early clinical diagnosis of sporadic CJD VV2 (ataxic type).
J Neurol Neurosurg Psychiatry
; 88(9): 764-772, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28668775
14.
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategy.
Acta Neuropathol
; 131(1): 87-102, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26659578
15.
Unusual presentations and intrafamilial phenotypic variability in infantile onset Alexander disease.
Neurol Sci
; 37(6): 973-7, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26743065
16.
Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis.
Hum Mol Genet
; 22(7): 1417-23, 2013 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23297359
17.
Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium.
J Neural Transm (Vienna)
; 122(7): 957-72, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25239189
18.
Anti-amyloid ß autoantibodies in cerebral amyloid angiopathy-related inflammation: implications for amyloid-modifying therapies.
Ann Neurol
; 73(4): 449-58, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23625526
19.
Early cortical and late striatal diffusion restriction on 3T MRI in a long-lived sporadic creutzfeldt-jakob disease case.
J Magn Reson Imaging
; 50(5): 1659-1662, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30912188
20.
Dissecting the Clinical Heterogeneity and Genotype-Phenotype Correlations of MAPT Mutations: A Systematic Review.
Front Biosci (Landmark Ed)
; 29(1): 12, 2024 01 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38287807