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2019 1
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Page 1
Uveitis and Multiple Sclerosis: Potential Common Causal Mutations.
de-la-Torre A, Silva-Aldana CT, Muñoz-Ortiz J, Piñeros-Hernández LB, Otero O, Domínguez A, Faciolince LA, Arcos-Holzinger M, Mastronardi C, Contreras-Bravo NC, Restrepo CM, Arcos-Burgos M. de-la-Torre A, et al. Among authors: arcos holzinger m. Mol Neurobiol. 2019 Dec;56(12):8008-8017. doi: 10.1007/s12035-019-1630-2. Epub 2019 Jun 3. Mol Neurobiol. 2019. PMID: 31161422 Free PMC article.
Correction: Uveitis and Multiple Sclerosis: Potential Common Causal Mutations.
de-la-Torre A, Silva-Aldana CT, Muñoz-Ortiz J, Piñeros-Hernández LB, Otero-Marquez O, Domínguez A, Faciolince LA, Arcos-Holzinger M, Mastronardi C, Contreras-Bravo NC, Restrepo CM, Arcos-Burgos M. de-la-Torre A, et al. Among authors: arcos holzinger m. Mol Neurobiol. 2023 May;60(5):2969. doi: 10.1007/s12035-023-03265-3. Mol Neurobiol. 2023. PMID: 36781740 Free PMC article. No abstract available.
Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings.
Aguillon D, Vasquez D, Madrigal L, Moreno S, Hernández D, Isaza-Ruget M, Lopez JJ, Landires I, Nuñez-Samudio V, Restrepo CM, Vidal OM, Vélez JI, Arcos-Holzinger M, Lopera F, Arcos-Burgos M. Aguillon D, et al. Among authors: arcos holzinger m. Mol Neurobiol. 2022 Jun;59(6):3845-3858. doi: 10.1007/s12035-022-02821-7. Epub 2022 Apr 14. Mol Neurobiol. 2022. PMID: 35420381
Correction to: Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings.
Aguillon D, Vasquez D, Madrigal L, Moreno S, Hernández D, Isaza-Ruget M, Lopez JJ, Landires I, Nunez-Samudio V, Restrepo CM, Vidal OM, Vélez JI, Arcos-Holzinger M, Lopera F, Arcos-Burgos M. Aguillon D, et al. Among authors: arcos holzinger m. Mol Neurobiol. 2022 Jun;59(6):3859. doi: 10.1007/s12035-022-02874-8. Mol Neurobiol. 2022. PMID: 35585447 No abstract available.
ADGRL3, FGF1 and DRD4: Linkage and Association with Working Memory and Perceptual Organization Candidate Endophenotypes in ADHD.
Cervantes-Henriquez ML, Acosta-López JE, Ahmad M, Sánchez-Rojas M, Jiménez-Figueroa G, Pineda-Alhucema W, Martinez-Banfi ML, Noguera-Machacón LM, Mejía-Segura E, De La Hoz M, Arcos-Holzinger M, Pineda DA, Puentes-Rozo PJ, Arcos-Burgos M, Vélez JI. Cervantes-Henriquez ML, et al. Among authors: arcos holzinger m. Brain Sci. 2021 Jun 26;11(7):854. doi: 10.3390/brainsci11070854. Brain Sci. 2021. PMID: 34206913 Free PMC article.
Calpainopathy: Description of a Novel Mutation and Clinical Presentation with Early Severe Contractures.
Landires I, Núñez-Samudio V, Fernandez J, Sarria C, Villareal V, Córdoba F, Apráez-Ippolito G, Martínez S, Vidal OM, Vélez JI, Arcos-Holzinger M, Landires S, Arcos-Burgos M. Landires I, et al. Among authors: arcos holzinger m. Genes (Basel). 2020 Jan 25;11(2):129. doi: 10.3390/genes11020129. Genes (Basel). 2020. PMID: 31991774 Free PMC article.