1. Hereditary ataxias and paraparesias: clinical and genetic update
   Livia Parodi et al, 2018, Current Opinion in Neurology CrossRef
2. Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches
   Samuel Shribman et al, 2019, The Lancet Neurology CrossRef
3. Illness representations, knowledge and motivation to perform presymptomatic testing for late-onset genetic diseases
   Ângela Leite et al, 2017, Psychology, Health & Medicine CrossRef
4. Oral trehalose maybe helpful for patients with spinocerebellar ataxia 3 and should be better evaluated
   M.A. Noorasyikin et al, 2020, Parkinsonism & Related Disorders CrossRef
5. Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force
   Connie Marras et al, 2016, Movement Disorders CrossRef
6. Corticospinal tract involvement in spinocerebellar ataxia type 3: a diffusion tensor imaging study
   Bruno Shigueo Yonekura Inada et al, 2021, Neuroradiology CrossRef
7. Clinical Features and Genetic Spectrum of Patients With Clinically Suspected Hereditary Progressive Spastic Paraplegia
   Yuzhi Shi et al, 2022, Frontiers in Neurology CrossRef