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SCA2
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An Electrophysiological Study of Visual Processing in Spinocerebellar Ataxia Type 2 (SCA2)
2011 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Medicine in Hradec Králové
publication
Can ataxin-2 be down-regulated by allele-specific de novo DNA methylation in SCA2 patients?
2004 |
Second Faculty of Medicine
publication
SCA2 trinucleotide expansion in German SCA patients
1997 |
Second Faculty of Medicine
publication
Morphological analysis of embryonic cerebellar grafts in SCA2 mice
2014 |
Faculty of Medicine in Pilsen
publication
An Electrophysiological Study of Visual Processing in Spinocerebellar Ataxia Type 2 (SCA2)
2011 |
Second Faculty of Medicine
publication
Mouse models of spinocerebellar ataxia type-2
2015 |
Faculty of Medicine in Pilsen
publication
Cognitive impairment in spinocerebellar ataxia type 2
2007 |
First Faculty of Medicine
publication
Spinocerebellar ataxia
2011 |
Faculty of Medicine in Hradec Králové
publication
Cognitive changes in spinocerebellar ataxia type 2
2011 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Medicine in Hradec Králové
publication
Cognitive impairment in spinocerebellar ataxia type 2
2007 |
Faculty of Medicine in Hradec Králové
publication
Cognitive changes in spinocerebellar ataxia type 2
2011 |
Second Faculty of Medicine
publication
Quantitative Oculomotor Assessment in Hereditary Ataxia: Discriminatory Power, Correlation with Severity Measures, and Recommended Parameters for Specific Genotypes
2024 |
Second Faculty of Medicine
publication
From mice to men: lessons from mutant ataxic mice
2014 |
Faculty of Medicine in Pilsen
publication
Fluorescent multiplex PCR: Fast method for autosomal dominant spinocerebellar ataxias screening
2005 |
Second Faculty of Medicine
publication
Spinocerebellar Ataxias Type 8, 12, and 17 and Dentatorubro-Pallidoluysian Atrophy in Czech Ataxic Patients
2013 |
First Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine
publication
SCA6 is caused by moderate CAG expansion in the alpha(1A)-voltage-dependent calcium channel gene
1997 |
Second Faculty of Medicine