Detalhe da pesquisa
1.
Clinical and Genetic Characterization of Brazilian Patients with Ataxia and Oculomotor Apraxia.
Mov Disord;
37(6): 1309-1316, 2022 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35426160
2.
Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegias.
Sci Rep;
11(1): 22248, 2021 11 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34782662
3.
Fields of Forel Brain Stimulation Improves Levodopa-Unresponsive Gait and Balance Disorders in Parkinson's Disease.
Neurosurgery;
89(3): 450-459, 2021 08 16.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34161592
4.
Ophthalmological changes in hereditary spastic paraplegia and other genetic diseases with spastic paraplegia.
J Neurol Sci;
409: 116620, 2020 Feb 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31865189
5.
A Case of NEDMAGA: Neurodevelopmental Disorder with Movement Abnormalities, Abnormal Gait, and Autistic Features.
Mov Disord Clin Pract;
11(2): 181-183, 2024 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38386481
6.
X-Linked Adrenoleukodystrophy Mimicking Hereditary Spastic Paraplegia.
Mov Disord Clin Pract;
7(1): 109-110, 2020 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31970225