Azevedo, O., Gago, M., Miltenberger-Miltenyi, G., Gaspar, P., et al. (2017). Mild left ventricular hypertrophy unravels a novel nonsense mutation of the GLA gene associated with the classical phenotype of fabry disease. Cardiology (Switzerland), 137(2), 67 - 73.

Vieira, N., Bessa, C., Rodrigues, A. J., Marques, P., et al. (2017). Sorting nexin 3 mutation impairs development and neuronal function in Caenorhabditis elegans. Cellular and Molecular Life Sciences.

Santos, M., Summavielle, T., Teixeira-Castro, A., Silva-Fernandes, A., et al. (2010). Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndrome. Neuroscience, 170(2), 453 - 467.

Alonso, I., Marques, J. M., Sousa, N., Sequeiros, J., et al. (2008). Motor and cognitive deficits in the heterozygous leaner mouse, a Cav2.1 voltage-gated Ca2+ channel mutant. Neurobiology of Aging, 29(11), 1733 - 1743.

Marques, F., Sousa, J. C., Correia-Neves, M., Oliveira, P., et al. (2007). The choroid plexus response to peripheral inflammatory stimulus. Neuroscience, 144(2), 424 - 430.

Mesquita, A. R., Pêgo, J. M., Summavielle, T., MacIel, P., et al. (2007). Neurodevelopment milestone abnormalities in rats exposed to stress in early life. Neuroscience, 147(4), 1022 - 1033.

MacIel, P., Cruz, V. T., Constante, M., Iniesta, I., et al. (2005). Neuroferritinopathy: Missense mutation in FTL causing early-onset bilateral pallidal involvement. Neurology, 65(4), 603 - 605.

Carlos Sousa, J., Grandela, C., Fernández-Ruiz, J., De Miguel, R., et al. (2004). Transthyretin is involved in depression-like behaviour and exploratory activity. Journal of Neurochemistry, 88(5), 1052 - 1058.