L. D. Locks-Coelho

Neurological phenotypes in spinocerebellar ataxia type 2: Role of mitochondrial polymorphism A10398G and other risk factors.

J. Pedroso, M. Saraiva-Pereira, L. Jardim, 2017, Parkinsonism & related disorders.

NESSCA Validation and Responsiveness of Several Rating Scales in Spinocerebellar Ataxia Type 2

J. Pedroso, M. Saraiva-Pereira, O. Barsottini, 2017, The Cerebellum.

Complex abdominal wall reconstruction after massive resection due to neoplastic invasion: a case report

L. Cavazzola, L. D. Locks-Coelho, Márcia Appel, 2021, Journal of surgical case reports.

ATXN3, ATXN7, CACNA1A, and RAI1 Genes and Mitochondrial Polymorphism A10398G Did Not Modify Age at Onset in Spinocerebellar Ataxia Type 2 Patients from South America

J. Pedroso, M. Saraiva-Pereira, E. Ribeiro, 2015, The Cerebellum.

The progression rate of spinocerebellar ataxia type 2 changes with stage of disease

J. Pedroso, M. Saraiva-Pereira, S. Camey, 2018, Orphanet Journal of Rare Diseases.

Increase of extracellular glutamate concentration increases its oxidation and diminishes glucose oxidation in isolated mouse hippocampus: Reversible by TFB‐TBOA

F. Hansen, F. V. Torres, L. D. Locks-Coelho, 2013, Journal of neuroscience research.