Functionality and disease severity in spinocerebellar ataxias
Author:
Affiliation:
1. Universidade Federal do Paraná, Brazil
2. University of Toronto, Canada
3. Universidade Federal do Paraná, Brazil; Universidade Federal do Paraná, Brazil
Abstract
Publisher
FapUNIFESP (SciELO)
Subject
Neurology,Neurology (clinical)
Link
http://www.scielo.br/pdf/anp/v80n2/1678-4227-anp-80-02-137.pdf
Reference31 articles.
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2. HeterozygousSTUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48);Genis D;Neurology,2018
3. Primary and secondary ataxias;Teive HAG;Curr Opin Neurol,2015
4. Spinocerebellar ataxia: relationship between phenotype and genotype: a review;Sun YM;Clin Genet,2016
5. Patients with autosomal dominant spinocerebellar ataxia have more risk of falls, important balance impairment, and decreased ability to function;Aizawa CYP;Arq Neuro-Psiquiatr,2013
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