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Neuropathology and Applied Neurobiology, ISSN 0305-1846, 04/2016, Volume 42, Issue 3, pp. 296 - 300
Journal Article
AKTUELLE NEUROLOGIE, ISSN 0302-4350, 11/2008, Volume 35, Issue 9, pp. 435 - 442
Episodic ataxias are a clinically and genetically heterogeneous group of diseases with cardinal symptoms comprising recurrent attacks of gait, stand or... 
CACNA1A GENE | CHROMOSOME 19P | calcium channels | POTASSIUM CHANNEL GENE | NEUROSCIENCES | CLINICAL NEUROLOGY | VESTIBULOCEREBELLAR ATAXIA | ion channel disorders | ataxia | potassium channels | PAROXYSMAL CEREBELLAR-ATAXIA | SMOOTH-PURSUIT | MUTATIONS | downbeat nystagmus | TYPE-2 | PROGRESSIVE ATAXIA
Journal Article
Journal Article
2012, Advances in Experimental Medicine and Biology, Volume 724, 17
The spinocerebellar ataxias (SCAs) are a group of neurodegenerative diseases characterised by progressive lack of motor coordination leading to major... 
MEDICINE, RESEARCH & EXPERIMENTAL | MOLECULAR CHAPERONES | POTASSIUM CHANNELOPATHY | NEUROSCIENCES | CLINICAL NEUROLOGY | VESTIBULOCEREBELLAR ATAXIA | TREMOR/ATAXIA SYNDROME | MOUSE MODEL | DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY | POLYGLUTAMINE AGGREGATION | DOMINANT CEREBELLAR-ATAXIA | HUNTINGTONS-DISEASE | EPISODIC ATAXIA
Book Chapter
Movement Disorders, ISSN 0885-3185, 05/2011, Volume 26, Issue 6, pp. 1157 - 1165
Journal Article
Journal Article
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