- Hereditary ataxias and paraparesias: clinical and genetic update
Livia Parodi et al, 2018, Current Opinion in Neurology CrossRef - Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches
Samuel Shribman et al, 2019, The Lancet Neurology CrossRef - Illness representations, knowledge and motivation to perform presymptomatic testing for late-onset genetic diseases
Ângela Leite et al, 2017, Psychology, Health & Medicine CrossRef - 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 - Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force
Connie Marras et al, 2016, Movement Disorders CrossRef - Investigating the genetic basis of hereditary spastic paraplegia and cerebellar Ataxia in Pakistani families
Arfa Azeem et al, 2024, BMC Neurology CrossRef - Disease Progression and Multiparametric Imaging Characteristics of Spinocerebellar Ataxia Type 3 With Spastic Paraplegia
Zhi-Xian Ye et al, 2024, Neurology Genetics CrossRef - Corticospinal tract involvement in spinocerebellar ataxia type 3: a diffusion tensor imaging study
Bruno Shigueo Yonekura Inada et al, 2021, Neuroradiology CrossRef - Clinical Features and Genetic Spectrum of Patients With Clinically Suspected Hereditary Progressive Spastic Paraplegia
Yuzhi Shi et al, 2022, Frontiers in Neurology CrossRef