França, M., Martí-Bonmatí, L., Silva, S., Oliveira, C., et al. (2017). Optimizing the management of hereditary haemochromatosis: The value of MRI R2* quantification to predict and monitor body iron stores. British Journal of Haematology.

Kazachkova, N., Raposo, M., Montiel, R., Cymbron, T., et al. (2013). Patterns of mitochondrial DNA damage in blood and brain tissues of a transgenic mouse model of machado-joseph disease. Neurodegenerative Diseases, 11(4), 206 - 214.

Alonso, I., Costa, C., Gomes, A., Ferro, A., et al. (2005). A novel H101Q mutation causes PKC? loss in spinocerebellar ataxia type 14. Journal of Human Genetics, 50(10), 523 - 529.