Detalhe da pesquisa
1.
Clinical and Genetic Features of Multiplex Families with Multiple System Atrophy and Parkinson's Disease.
Cerebellum
; 2022 Sep 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36097244
2.
Memory impairment following right cerebellar infarction: a case study.
Neurocase
; 21(5): 660-4, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25350282
3.
Tumefactive multiple sclerosis which initially presented with brainstem encephalitis with a long-term follow-up.
Mult Scler Relat Disord
; 32: 23-26, 2019 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-31005827
4.
The pathogenesis linked to coenzyme Q10 insufficiency in iPSC-derived neurons from patients with multiple-system atrophy.
Sci Rep
; 8(1): 14215, 2018 09 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-30242188
5.
Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy.
Nat Genet
; 50(4): 581-590, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29507423
6.
Atypical parkinsonism caused by Pro105Leu mutation of prion protein: A broad clinical spectrum.
Neurol Genet
; 2(1): e48, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27066585