Multiple system atrophy in a patient with the spinocerebellar ataxia 3 gene mutation

2007 ◽  
Vol 22 (2) ◽  
pp. 251-253 ◽  
Author(s):  
Melissa J. Nirenberg ◽  
Jenny Libien ◽  
Jean-Paul Vonsattel ◽  
Stanley Fahn
Keyword(s):  
Multiple System Atrophy ◽  
Gene Mutation ◽  
Spinocerebellar Ataxia ◽  
Spinocerebellar Ataxia 3

Analysis of SCA3/MJD3 gene mutation and genetic polymorphism in a Guangxi family with spinocerebellar ataxia 3

2013 ◽  
Vol 35 (11) ◽  
pp. 1300-1306
Author(s):  
Rong-Ni CHANG ◽  
Guang-Zhi YUAN ◽  
Jian-Qiang TAN ◽  
Qing-Niao LAI ◽  
Jun MA ◽  
...  
Keyword(s):  
Genetic Polymorphism ◽  
Gene Mutation ◽  
Spinocerebellar Ataxia ◽  
Spinocerebellar Ataxia 3

scholarly journals Novel SPTBN2 gene mutation and first intragenic deletion in early onset spinocerebellar ataxia type 5

2021 ◽  
Vol 8 (4) ◽  
pp. 956-963
Author(s):  
Romina Romaniello ◽  
Andrea Citterio ◽  
Elena Panzeri ◽  
Filippo Arrigoni ◽  
Marta De Rinaldis ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Spinocerebellar Ataxia ◽  
Early Onset ◽  
Spinocerebellar Ataxia Type ◽  
Intragenic Deletion

Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy

2021 ◽  
Vol 31 (1) ◽  
pp. 117-125
Author(s):  
Anna I. Wernick ◽  
Ronald L. Walton ◽  
Alexandra I. Soto-Beasley ◽  
Shunsuke Koga ◽  
Michael G. Heckman ◽  
...  
Keyword(s):  
Multiple System Atrophy ◽  
Spinocerebellar Ataxia

Unusual nocturnal motor restlessness in a patient with spinocerebellar ataxia 3

2005 ◽  
Vol 20 (7) ◽  
pp. 899-901 ◽  
Author(s):  
Imad Ghorayeb ◽  
Federica Provini ◽  
Bernard Bioulac ◽  
François Tison
Keyword(s):  
Spinocerebellar Ataxia ◽  
Motor Restlessness ◽  
Spinocerebellar Ataxia 3
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