Mild left ventricular hypertrophy unravels a novel nonsense mutation of the GLA gene associated with the classical phenotype of fabry disease - Azevedo, O.; Gago, M.; Miltenberger-Miltenyi, G.; Gaspar, P.; Sousa, N.; Cunha, D. (Cardiology (Switzerland), 2017)

Serum lipid alterations in GBA-associated Parkinson's disease - Guedes, L.C.; Chan, R.B.; Gomes, M.A.; Conceição, V.A.; Machado, R.B.; Soares, T.; Xu, Y.; Gaspar, P.; Carriço, J.A.; Alcalay, R.N.; Ferreira, J.J.; Outeiro, T.F.; et al. (Parkinsonism and Related Disorders, 2017)