Detalhe da pesquisa
1.
APOE4 impairs myelination via cholesterol dysregulation in oligodendrocytes.
Nature;
611(7937): 769-779, 2022 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36385529
2.
Fibrillation and molecular characteristics are coherent with clinical and pathological features of 4-repeat tauopathy caused by MAPT variant G273R.
Neurobiol Dis;
146: 105079, 2020 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32961270
3.
Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates.
Acta Neuropathol;
139(4): 717-734, 2020 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31950334
4.
De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions.
Am J Hum Genet;
98(4): 763-71, 2016 Apr 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27058447
5.
The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort.
Hum Mol Genet;
24(18): 5326-9, 2015 Sep 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26157024
6.
PREDICT-PD: An online approach to prospectively identify risk indicators of Parkinson's disease.
Mov Disord;
32(2): 219-226, 2017 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28090684
7.
Aberrant axon initial segment plasticity and intrinsic excitability of ALS hiPSC motor neurons.
Cell Rep;
42(12): 113509, 2023 12 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38019651
8.
Biobased Elastomer Nanofibers Guide Light-Controlled Human-iPSC-Derived Skeletal Myofibers.
Adv Mater;
34(18): e2110441, 2022 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35231133
9.
ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients.
Parkinsonism Relat Disord;
41: 37-43, 2017 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28511835