- Clinicopathological description of two cases with SQSTM1 gene mutation associated with frontotemporal dementia2016 | 1. lékařská fakulta, 2. lékařská fakulta
- Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration2014 | 1. lékařská fakulta
- Oligodendroglial Response in the Spinal Cord in TDP-43 Proteinopathy with Motor Neuron Involvement2014 | 1. lékařská fakulta, 3. lékařská fakulta
- Ex vivo 3D human corneal stroma model for Schnyder corneal dystrophy - role of autophagy in its pathogenesis and resolution2018 | 1. lékařská fakulta