Detalhe da pesquisa
1.
Selective visuoconstructional impairment following mild COVID-19 with inflammatory and neuroimaging correlation findings.
Mol Psychiatry
; 28(2): 553-563, 2023 02.
Artigo
Inglês
| MEDLINE | ID: mdl-35701598
2.
Development and Validation of the Dystonia-Pain Classification System: A Multicenter Study.
Mov Disord
; 38(7): 1163-1174, 2023 07.
Artigo
Inglês
| MEDLINE | ID: mdl-37208983
3.
A comparative study of cognitive and behavioral profiles between sporadic and type 8 amyotrophic lateral sclerosis.
Muscle Nerve
; 68(3): 316-322, 2023 09.
Artigo
Inglês
| MEDLINE | ID: mdl-37424512
4.
Episodic memory in progressive supranuclear palsy: a neuropsychological and neuroimaging study.
Neurol Sci
; 43(9): 5363-5368, 2022 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-35633422
5.
Characterisation of ataxia in Sjogren's syndrome.
J Neurol Neurosurg Psychiatry
; 91(4): 446-448, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-32015088
6.
Comparison of techniques of botulinum toxin injections for blepharospasm and hemifacial spasm.
Mov Disord
; 34(9): 1401-1403, 2019 09.
Artigo
Inglês
| MEDLINE | ID: mdl-31251420
7.
Handicap as a Measure of Perceived-Health Status in Parkinson's Disease.
Mov Disord Clin Pract
; 10(8): 1172-1180, 2023 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-37635780
8.
Do Patients with Progressive Supranuclear Palsy Have Episodic Memory Impairment? A Systematic Review.
Mov Disord Clin Pract
; 9(4): 436-445, 2022 May.
Artigo
Inglês
| MEDLINE | ID: mdl-35586534
9.
Structural brain and spinal cord damage in symptomatic and pre-symptomatic VAPB-related ALS.
J Neurol Sci
; 434: 120126, 2022 Mar 15.
Artigo
Inglês
| MEDLINE | ID: mdl-35007920
10.
I'm looking through you: Mentalizing in frontotemporal dementia and progressive supranuclear palsy.
Cortex
; 155: 373-389, 2022 10.
Artigo
Inglês
| MEDLINE | ID: mdl-36116296
11.
Rare mutations in ATL3, SPTLC2 and SCN9A explaining hereditary sensory neuropathy and congenital insensitivity to pain in a Brazilian cohort.
J Neurol Sci
; 427: 117498, 2021 Aug 15.
Artigo
Inglês
| MEDLINE | ID: mdl-34090020
12.
Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.
Mov Disord
; 24(5): 662-6, 2009 Apr 15.
Artigo
Inglês
| MEDLINE | ID: mdl-19205068
13.
Amyotrophic lateral sclerosis type 8 is not a pure motor disease: evidence from a neuropsychological and behavioural study.
J Neurol
; 266(8): 1980-1987, 2019 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-31089860
14.
Novel GCH1 mutation in a Brazilian family with dopa-responsive dystonia.
Mov Disord
; 23(2): 299-302, 2008 Jan 30.
Artigo
Inglês
| MEDLINE | ID: mdl-18044725
15.
POLG1 Arg953Cys mutation: expanded phenotype and recessive inheritance in a Brazilian family.
Muscle Nerve
; 45(3): 453-4, 2012 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-22334187
16.
A Brazilian family with Brown-Vialetto-van Laere syndrome with autosomal recessive inheritance.
Arq Neuropsiquiatr
; 65(1): 32-5, 2007 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-17420823
17.
The genetics of the dystonias--a review based on the new classification of the dystonias.
Arq Neuropsiquiatr
; 73(4): 350-8, 2015 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-25992527
18.
Internal consistency of a Brazilian version of the unified Huntington's disease rating scale.
Arq Neuropsiquiatr
; 62(4): 977-82, 2004 12.
Artigo
Inglês
| MEDLINE | ID: mdl-15608955
19.
Genetic evaluation for TOR1-A (DYT1) in Brazilian patients with dystonia.
Arq Neuropsiquiatr
; 72(10): 753-6, 2014 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-25337725
20.
Cervical dystonia: about familial and sporadic cases in 88 patients.
Arq Neuropsiquiatr
; 72(2): 107-13, 2014 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-24604363