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List of works by Chantal M E Tallaksen

A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42).

scientific article

Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia

scientific article

Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia

scientific article

Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10.

scientific article published in February 2009

Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes

scientific article published on 26 February 2018

Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia

scientific article published on 10 November 2006

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration

scientific article published on 13 December 2007

Survival and severity in dominant cerebellar ataxias

scientific article

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