Spinocerebellar ataxia type 3 presenting with writer's cramp without ataxia
Author:
Affiliation:
1. Neurology Department, Hospital Universitario 12 de Octubre, Madrid, Spain
2. Movement Disorders Unit, Hospital Universitario 12 de Octubre, Madrid, Spain
3. Centro De Investigación Biomédica En Red sobre Enfermedades Neurodegenerativas, Spain
Publisher
Informa UK Limited
Subject
General Medicine,General Neuroscience
Link
https://www.tandfonline.com/doi/pdf/10.1080/00207454.2017.1408621
Reference5 articles.
1. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis
2. Intrafamilial variability in Machado-Joseph disease
3. Autosomal dominant system degeneration in Portuguese families of the Azores Islands: A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions
4. Chinese patients with spinocerebellar ataxia type 3 presenting with rare clinical symptoms
5. Dystonia in Machado–Joseph disease: Clinical profile, therapy and anatomical basis
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2. Deep brain stimulation for patients with dystonia in Machado–Joseph disease: three case reports;Journal of Neurology;2023-03-02
3. Pharmacotherapy for the management of the symptoms of Machado-Joseph Disease;Expert Opinion on Pharmacotherapy;2022-10-13
4. Botulinum neurotoxin for writer’s cramp;Annals of Movement Disorders;2022-09
5. Unraveling movement disorders in spinocerebellar ataxia;Annals of Movement Disorders;2022-05
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