Detalhe da pesquisa
1.
Frequency of Hereditary and GBA1-Related Parkinsonism in Latin America: A Systematic Review and Meta-Analysis.
Mov Disord;
39(1): 6-16, 2024 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37921246
2.
Genome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients.
Mov Disord;
36(2): 434-441, 2021 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33150996
3.
The Parkinson's Disease Genome-Wide Association Study Locus Browser.
Mov Disord;
35(11): 2056-2067, 2020 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32864809
4.
Predictors of Motor Complications in Early Parkinson's Disease.
Mov Disord;
35(1): 191-192, 2020 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31965634
5.
Polymorphisms in the dopamine transporter gene are associated with visual hallucinations and levodopa equivalent dose in Brazilians with Parkinson's disease.
Int J Neuropsychopharmacol;
16(6): 1251-1258, 2013 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23363854
6.
Average annual cost of Parkinson's disease in a Brazilian multiethnic population.
Parkinsonism Relat Disord;
117: 105897, 2023 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37931350
7.
Lack of full sequencing GBA1 studies for patients with Parkinson's disease in Latin America.
NPJ Parkinsons Dis;
8(1): 101, 2022 Aug 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35941142
8.
Parkinsonism-hyperpyrexia Syndrome After Amantadine Withdrawal: Case Report and Review of the Literature.
Neurologist;
26(4): 149-152, 2021 Jul 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34190209
9.
Diagnostic prediction model for levodopa-induced dyskinesia in Parkinson's disease.
Arq Neuropsiquiatr;
78(4): 206-216, 2020 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32294749
10.
Genetic Testing for Parkinson's Disease and Movement Disorders in Less Privileged Areas: Barriers and Opportunities.
Mov Disord Clin Pract;
11(1): 14-20, 2024 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38291851
11.
Tumor necrosis factor alpha polymorphisms are associated with Parkinson's disease age at onset.
Neurosci Lett;
658: 133-136, 2017 Sep 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28844731
12.
Association between DNA methyltransferase gene polymorphism and Parkinson's disease.
Neurosci Lett;
639: 146-150, 2017 02 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28041964
13.
Val66Met BDNF polymorphism is associated with Parkinson's disease cognitive impairment.
Neurosci Lett;
615: 88-91, 2016 Feb 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26806863
14.
Influence of genetic, biological and pharmacological factors on levodopa dose in Parkinson's disease.
Pharmacogenomics;
17(5): 481-8, 2016 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27019953
15.
Is there a role for ADORA2A polymorphisms in levodopa-induced dyskinesia in Parkinson's disease patients?
Pharmacogenomics;
16(6): 573-82, 2015.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25872644
16.
Parkinson's disease pharmacogenomics: new findings and perspectives.
Pharmacogenomics;
15(9): 1253-71, 2014 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25141900
17.
DNA methyltransferase haplotype is associated with Alzheimer's disease.
Neurosci Lett;
579: 70-4, 2014 Sep 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25038421
18.
DRD2 haplotype is associated with dyskinesia induced by levodopa therapy in Parkinson's disease patients.
Pharmacogenomics;
13(15): 1701-10, 2012 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23171335
19.
Sex differential effect of parental longevity on the risk of dementia.
J Am Geriatr Soc;
62(2): 393-5, 2014 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24521375