Cavity filling mutations at the thyroxine-binding site dramatically increase transthyretin stability and prevent its aggregation - Sant'Anna, R.; Almeida, M.R.; Varejao, N.; Gallego, P.; Esperante, S.; Ferreira, P.; Pereira-Henriques, A.; Palhano, F.L.; De Carvalho, M.; Foguel, D.; Reverter, D.; Saraiva, M.J.; et al. (Scientific Reports, 2017)

Mutant fibrinogen A-α-chain associated with hereditary renal amyloidosis and peripheral neuropathy - De Carvalho, M.; Linke, R.P.; Domingos, F.; Evangelista, T.; Ducla-Soares, J.L.; Nathrath, W.B.J.; Azevedo-Coutinho, C.; Lima, R.; Saraiva, M.J. (Amyloid, 2004)