Mauricio Arcos-Holzinger

Calpainopathy: Description of a Novel Mutation and Clinical Presentation with Early Severe Contractures

M. Arcos-Burgos, J. I. Velez, I. Landires, 2020, Genes.

Uveitis and Multiple Sclerosis: Potential Common Causal Mutations

M. Arcos-Burgos, C. Restrepo, A. de-la-Torre, 2019, Molecular Neurobiology.

ADGRL3, FGF1 and DRD4: Linkage and Association with Working Memory and Perceptual Organization Candidate Endophenotypes in ADHD

D. Pineda, M. Arcos-Burgos, Giomar Jiménez-Figueroa, 2021, Brain sciences.

A Comprehensive Machine Learning Framework for the Exact Prediction of the Age of Onset in Familial and Sporadic Alzheimer’s Disease

F. Lopera, M. Arcos-Burgos, J. I. Velez, 2021, Diagnostics.

Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings

F. Lopera, M. Arcos-Burgos, C. Restrepo, 2022, Molecular Neurobiology.

Utility of a Short Neuropsychological Protocol for Detecting HIV-Associated Neurocognitive Disorders in Patients with Asymptomatic HIV-1 Infection

Manuel Perea, M. Arcos-Burgos, J. E. Acosta-López, 2021, Brain sciences.

Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings

F. Lopera, M. Arcos-Burgos, C. Restrepo, 2021, Molecular Neurobiology.