- Clinicopathological description of two cases with SQSTM1 gene mutation associated with frontotemporal dementia2016 | First Faculty of Medicine, Second Faculty of Medicine
- Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration2014 | First Faculty of Medicine
- Oligodendroglial Response in the Spinal Cord in TDP-43 Proteinopathy with Motor Neuron Involvement2014 | First Faculty of Medicine, Third Faculty of Medicine
- Ex vivo 3D human corneal stroma model for Schnyder corneal dystrophy - role of autophagy in its pathogenesis and resolution2018 | First Faculty of Medicine