Detalhe da pesquisa
1.
Clinicopathological correlates in frontotemporal lobar degeneration: motor neuron disease spectrum.
Brain
; 2024 Jan 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38227807
2.
Amyloid precursor protein ð½CTF accumulates in synapses in sporadic and genetic forms of Alzheimer's disease.
Neuropathol Appl Neurobiol
; 49(1): e12879, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36702749
3.
Myelin loss in C9orf72 hexanucleotide expansion carriers.
J Neurosci Res
; 100(10): 1862-1875, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35766328
4.
Neuropathology of a patient with Alzheimer disease treated with low doses of verubecestat.
Neuropathol Appl Neurobiol
; 48(3): e12781, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34825396
5.
Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers.
Acta Neuropathol
; 144(5): 821-842, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36066633
6.
Heterozygous APOE Christchurch in familial Alzheimer's disease without mutations in other Mendelian genes.
Neuropathol Appl Neurobiol
; 47(4): 579-582, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33095930
7.
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.
Mov Disord
; 34(12): 1851-1863, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31660654
8.
Analysis of known amyotrophic lateral sclerosis and frontotemporal dementia genes reveals a substantial genetic burden in patients manifesting both diseases not carrying the C9orf72 expansion mutation.
J Neurol Neurosurg Psychiatry
; 89(2): 162-168, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28889094
9.
Distinct Clinical Features and Outcomes in Motor Neuron Disease Associated with Behavioural Variant Frontotemporal Dementia.
Dement Geriatr Cogn Disord
; 45(3-4): 220-231, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29886477
10.
Characterization of the repeat expansion size in C9orf72 in amyotrophic lateral sclerosis and frontotemporal dementia.
Hum Mol Genet
; 23(3): 749-54, 2014 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24057670
11.
Plasma phosphorylated TDP-43 levels are elevated in patients with frontotemporal dementia carrying a C9orf72 repeat expansion or a GRN mutation.
J Neurol Neurosurg Psychiatry
; 85(6): 684-91, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24309270
12.
Dissecting phenotypic traits linked to human resilience to Alzheimer's pathology.
Brain
; 136(Pt 8): 2510-26, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23824488
13.
APOE4 homozygozity represents a distinct genetic form of Alzheimer's disease.
Nat Med
; 30(5): 1284-1291, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38710950
14.
Analysis of the C9orf72 gene in patients with amyotrophic lateral sclerosis in Spain and different populations worldwide.
Hum Mutat
; 34(1): 79-82, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22936364
15.
Proteomic comparison between non-purified cerebrospinal fluid and cerebrospinal fluid-derived extracellular vesicles from patients with Alzheimer's, Parkinson's and Lewy body dementia.
J Extracell Vesicles
; 12(12): e12383, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38082559
16.
Reduced Number of Thymoma CTLA4-Positive Cells Is Associated With a Higher Probability of Developing Myasthenia Gravis.
Neurol Neuroimmunol Neuroinflamm
; 10(2)2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36697230
17.
Neuroinflammation-Related Proteins NOD2 and Spp1 Are Abnormally Upregulated in Amyotrophic Lateral Sclerosis.
Neurol Neuroimmunol Neuroinflamm
; 10(2)2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36460480
18.
Brain hypometabolism in non-demented microtubule-associated protein tau H1 carriers with Parkinson's disease.
J Neuroimaging
; 33(6): 953-959, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37726927
19.
Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control Studies.
Neurol Genet
; 9(4): e200079, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37293291
20.
Erratum: Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control Studies.
Neurol Genet
; 9(5): e200095, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37521204