Blindness and Deafness – an Extreme Phenotype in Friedreich Ataxia
Midbrain atrophy related to parkinsonism in a non-coding repeat expansion disorder: five cases of spinocerebellar ataxia type 31 with nigrostriatal dopaminergic dysfunction
Idiopathic Superficial Siderosis of the Central Nervous System
Genetic Rhabdomyolysis within the Spectrum of the Spinocerebellar Ataxia Type 2 Responsive to Pregabalin
Cerebellar transcranial direct current stimulation reconfigurates static and dynamic functional connectivity of the resting-state networks
An Unusual Case of Myasthenia-Like Presentation in Erdheim-Chester Disease
Should we Investigate Mitochondrial Disorders in Progressive Adult-onset Undetermined Ataxias?
Relationships between motor scores and cognitive functioning in FMR1 female premutation X carriers indicate early involvement of cerebello-cerebral pathways.
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