Author:
Rodríguez-Antigüedad Jon,Pérez-Pérez Jesús,Kulisevsky Jaime
Publisher
Springer International Publishing
Reference63 articles.
1. Alami, N. H., Smith, R. B., Carrasco, M. A., Williams, L. A., Winborn, C. S., Han, S. S. W., et al. (2014). Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations. Neuron, 81(3), 536–543.
2. Arnold, E. S., Ling, S. C., Huelga, S. C., Lagier-Tourenne, C., Polymenidou, M., Ditsworth, D., et al. (2013a). ALS-linked TDP-43 mutations produce aberrant RNA splicing and adult-onset motor neuron disease without aggregation or loss of nuclear TDP-43. Proceedings of the National Academy of Sciences of the United States of America, 110(8), E736–E745.
3. Arnold, S. J., Dugger, B. N., & Beach, T. G. (2013b). TDP-43 deposition in prospectively followed, cognitively normal elderly individuals: Correlation with argyrophilic grains but not other concomitant pathologies. Acta Neuropathologica, 126(1), 51–57.
4. Ballatore, C., Lee, V. M. Y., & Trojanowski, J. Q. (2007). Tau-mediated neurodegeneration in Alzheimer’s disease and related disorders. Nature Reviews. Neuroscience, 8(9), 663–672.
5. Banfi, S., Servadio, A., Chung, M. Y., Kwiatkowski, T. J., McCall, A. E., Duvick, L. A., et al. (1994). Identification and characterization of the gene causing type 1 spinocerebellar ataxia. Nature Genetics, 7(4), 513–520.