Detalhe da pesquisa
1.
Wall permeability on magnetic resonance imaging is associated with intracranial aneurysm symptoms and wall enhancement.
Eur Radiol
; 2024 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38224377
2.
Spinocerebellar Ataxia Type 10 with Atypical Clinical Manifestation in Han Chinese.
Cerebellum
; 22(3): 355-362, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35441258
3.
ß-arrestin interacts with TRAF6 to negatively regulate the NF-κB pathway in triangle sail mussel Hyriopsis cumingii.
Fish Shellfish Immunol
; 127: 65-73, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35705131
4.
Disrupted structure and aberrant function of CHIP mediates the loss of motor and cognitive function in preclinical models of SCAR16.
PLoS Genet
; 14(9): e1007664, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30222779
5.
CADASIL mutant NOTCH3(R90C) decreases the viability of HS683 oligodendrocytes via apoptosis.
Mol Biol Rep
; 44(3): 273-280, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28601945
6.
Exome capture sequencing identifies a novel CCM1 mutation in a Chinese family with multiple cerebral cavernous malformations.
Int J Neurosci
; 126(12): 1071-6, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26643368
7.
Mapping of repeat-associated non-AUG (RAN) translation knowledge: A bibliometric analysis.
Heliyon
; 10(8): e29141, 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38628764
8.
Detection of skin α-synuclein using RT-QuIC as a diagnostic biomarker for Parkinson's disease in the Chinese population.
Eur J Med Res
; 29(1): 114, 2024 Feb 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38336827
9.
Dynamic monitoring of UBA1 somatic mutations in patients with relapsing polychondritis.
Orphanet J Rare Dis
; 19(1): 1, 2024 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38167209
10.
Novel inflammatory and insulin resistance indices provide a clue in cerebral amyloid angiopathy.
Sci Rep
; 14(1): 11474, 2024 05 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38769356
11.
Peripheral cutaneous synucleinopathy characteristics in genetic Parkinson's disease.
Front Neurol
; 15: 1404492, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38751879
12.
Regional and age-dependent changes in ubiquitination in cellular and mouse models of spinocerebellar ataxia type 3.
Front Mol Neurosci
; 16: 1154203, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37122622
13.
Regional and age-dependent changes in ubiquitination in cellular and mouse models of Spinocerebellar ataxia type 3.
bioRxiv
; 2023 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36891289
14.
Seed amplification assay of nasal swab extracts for accurate and non-invasive molecular diagnosis of neurodegenerative diseases.
Transl Neurodegener
; 12(1): 13, 2023 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36922862
15.
CHCHD2 p.Thr61Ile knock-in mice exhibit motor defects and neuropathological features of Parkinson's disease.
Brain Pathol
; 33(3): e13124, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36322611
16.
Neuroinflammation in Parkinson's Disease: Triggers, Mechanisms, and Immunotherapies.
Neuroscientist
; 28(4): 364-381, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33576313
17.
Clinical application of prion-like seeding in α-synucleinopathies: Early and non-invasive diagnosis and therapeutic development.
Front Mol Neurosci
; 15: 975619, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36299857
18.
Dysregulation of peripheral monocytes and pro-inflammation of alpha-synuclein in Parkinson's disease.
J Neurol
; 269(12): 6386-6394, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-35895134
19.
Pseudo-dominant inheritance of a novel double GLA mutation associated with Fabry disease mimicking familial episodic pain.
Am J Med Genet A
; 170(11): 3051-3053, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27531472
20.
Deciphering Neurodegenerative Diseases Using Long-Read Sequencing.
Neurology
; 97(9): 423-433, 2021 08 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-34389649