共 182 条
- [1] Sullivan R(2019)Spinocerebellar ataxia: an update J Neurol 266 533-544
- [2] Yau WY(2021)Tezenas du Montcel S, Klockgether T. Natural history of most common spinocerebellar ataxia: a systematic review and meta-analysis J Neurol 268 2749-2756
- [3] O'Connor E(2014)The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies Neuroepidemiology. 42 174-183
- [4] Houlden H(2015)Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study Lancet Neurol 14 1101-1108
- [5] Diallo A(2022)Quality of life since pre-ataxic phases of spinocerebellar ataxia type 3/Machado-Joseph disease Cerebellum. 21 297-305
- [6] Jacobi H(2014)Patient-reported outcome (PRO) assessment in clinical trials: a systematic review of guidance for trial protocol writers PLoS One 9 e110216-292
- [7] Ruano L(2009)The use of patient-reported outcomes instruments in registered clinical trials: evidence from ClinicalTrials.gov Contemp Clin Trials 30 289-128
- [8] Melo C(2008)Health related quality of life measures in Friedreich ataxia J Neurol Sci 272 123-2051
- [9] Silva MC(2018)Long-term evolution of patient-reported outcome measures in spinocerebellar ataxias J Neurol 265 2040-895
- [10] Coutinho P(2021)Discordance between patient-reported outcomes and physician-rated motor symptom severity in early-to-middle-stage spinocerebellar ataxia type 3 Cerebellum. 20 887-595