Author:
Braga-Neto P.,Felicio A.C.,Pedroso J.L.,Dutra L.A.,Bertolucci P.H.F.,Gabbai A.A.,Barsottini O.G.P.
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference29 articles.
1. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis;Schöls;Lancet Neurol,2004
2. Frequency of different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients;Lopes-Cendes;Arq Neuropsiquiatr,1997
3. Clinical phenotype of Brazilian families with spinocerebellar ataxia 10;Teive;Neurology,2004
4. Clinical criteria for diagnosis of Machado-Joseph disease: report of a non-Azorean Portuguese family;Lima;Neurology,1980
5. Neurologic findings in Machado-Joseph disease: relation with disease duration, subtypes, and (CAG)n;Jardim;Arch Neurol,2001
Cited by
29 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献