Parkinsonism and ataxia
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference140 articles.
1. Movement disorders in autosomal dominant cerebellar ataxias: a systematic review;Rossi;Mov Disord Clin Pract,2014
2. SCA-2 presenting as parkinsonism in an Alberta family: clinical, genetic, and PET findings;Furtado;Neurology,2002
3. Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism;Shan;Ann. Neurol.,2001
4. The parkinsonian phenotype of spinocerebellar ataxia type 2;Lu;Arch. Neurol.,2004
5. Spinocerebellar ataxia type 2: Clinicogenetic aspects, mechanistic insights, and management approaches;Velazquez-Perez;Front. Neurol.,2017
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1. Identification of SYNJ1 in a Complex Case of Juvenile Parkinsonism Using a Multiomics Approach;International Journal of Molecular Sciences;2024-09-09
2. Clinical and Molecular Spectrum of Autosomal Recessive CA8‐Related Cerebellar Ataxia;Movement Disorders;2024-04-06
3. Imbalance and gait impairment in Parkinson’s disease: discussing postural instability and ataxia;Neurological Sciences;2023-11-21
4. Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders;Brain;2023-11-10
5. Parkinsonism in complex neurogenetic disorders: lessons from hereditary dementias, adult-onset ataxias and spastic paraplegias;Neurological Sciences;2023-08-30
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