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10.1007/s12311-019-01042-4

Deafness and Vestibulopathy in Cerebellar Diseases: a Practical Approach



Twenty Years of a Pre-Symptomatic Testing Protocol for Late-Onset Neurological Diseases in Portugal.



Eye Movement Abnormalities in Neurodegenerative Diseases


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10.1007/s10072-019-03970-9

Highlights of the issue 7, 2019


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10.1007/s10048-019-00565-6

Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes



Phenotypic and Genotypic Analysis of Hereditary Ataxia Patients in Sakarya City, Turkey.



Profiling the genome-wide landscape of tandem repeat expansions


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10.1007/s11910-019-0968-1

Sleep Disorders in Hereditary Ataxias



Prevalence and phenotype of the c.1529C>T SPG7 variant in adult‐onset cerebellar ataxia in Italy


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10.1097/WCO.0000000000000735

Charcot-Marie-Tooth disease and related disorders: an evolving landscape.


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10.1016/j.nbd.2019.104606

Friedreich ataxia- pathogenesis and implications for therapies


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10.1007/s10072-019-03856-w

Degenerative and acquired sporadic adult onset ataxia


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10.1038/s41588-019-0387-x

Expanding the genetic basis of ataxia



Hereditary Ataxia with a Novel Mutation in the Senataxin Gene: A Case Report


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10.1134/S1022795419030062

DNA Methylation in Neurodegenerative Diseases


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