Add to ORKGCopyright © 2014 Georgios Koutsis et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Introduction. Spinocerebellar ataxia 17 (SCA 17) is a rare autosomal dominant cerebellar ataxia (ADCA) caused by a CAG/CAA expansion in the TBP gene, reported from a limited number of countries. It is a very heterogeneous ADCA characterized by ataxia, cognitive decline, psychiatric symptoms, and involuntary movements, with some patients presenting with Huntington disease (HD) phenocopies. The SCA 17 expansion is stable during parent-child transmission and intrafamilial phenotypic homogenei...
Item does not contain fulltextBACKGROUND: Autosomal dominant cerebellar ataxias (ADCAs), or spinocer...
ABSTRACT- The spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous group of...
The autosomal dominant spinocerebellar ataxias (SCAs) are a clinically heterogeneous group of neurod...
Contains fulltext : 50955.pdf (publisher's version ) (Closed access)We describe cl...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
Spinocerebellar ataxias are classified according to the clinical signs, affected neuroanatomical reg...
Introduction: Spinocerebellar ataxia 48 has recently been described as an adult onset ataxia associa...
International audienceSpinocerebellar ataxia 17 (SCA17) or Huntington's disease-like-4 is a neurodeg...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
BACKGROUND: Spinocerebellar ataxia type 17 is an autosomal dominant cerebellar ataxia caused by a CA...
Item does not contain fulltextBACKGROUND: Autosomal dominant cerebellar ataxias (ADCAs), or spinocer...
ABSTRACT- The spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous group of...
The autosomal dominant spinocerebellar ataxias (SCAs) are a clinically heterogeneous group of neurod...
Contains fulltext : 50955.pdf (publisher's version ) (Closed access)We describe cl...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
Spinocerebellar ataxias are classified according to the clinical signs, affected neuroanatomical reg...
Introduction: Spinocerebellar ataxia 48 has recently been described as an adult onset ataxia associa...
International audienceSpinocerebellar ataxia 17 (SCA17) or Huntington's disease-like-4 is a neurodeg...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
Spinocerebellar ataxia type 17 (SCA17) is a rare autosomal dominant neurodegenerative disease caused...
BACKGROUND: Spinocerebellar ataxia type 17 is an autosomal dominant cerebellar ataxia caused by a CA...
Item does not contain fulltextBACKGROUND: Autosomal dominant cerebellar ataxias (ADCAs), or spinocer...
ABSTRACT- The spinocerebellar ataxias (SCAs) are a clinically and genetically heterogeneous group of...
The autosomal dominant spinocerebellar ataxias (SCAs) are a clinically heterogeneous group of neurod...