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The Lancet. Neurology|August 21, 2010
Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyondAlexandra DurrCurrent Opinion in Neurobiology|August 17, 2021
Genetics in hereditary spastic paraplegias: Essential but not enoughFrédéric Darios, Giulia Coarelli, Alexandra DurrF1000Research|November 27, 2018
Recent advances in understanding dominant spinocerebellar ataxias from clinical and genetic points of viewGiulia Coarelli, Alexis Brice, Alexandra DurrThe Lancet. Neurology|July 21, 2023
Autosomal dominant cerebellar ataxias: new genes and progress towards treatmentsGiulia Coarelli, Marie Coutelier, Alexandra DurrFaculty Reviews|April 5, 2021
Recent advances in understanding hereditary spastic paraplegias and emerging therapiesPauline Lallemant-Dudek, Frederic Darios, Alexandra DurrEuropean Journal of Human Genetics : EJHG|September 13, 2018
Reverse pre-symptomatic testing for Huntington disease: double disclosure when 25% at-risk children reveal the genetic status to their parentAdeline Bonnard, Ariane Herson, Marcela Gargiulo, et al.Current Opinion in Neurology|November 10, 2007
Hereditary spastic paraplegias: an updateChristel Depienne, Giovanni Stevanin, Alexis Brice, et al.Plos One|April 13, 2011
Altered dopamine and serotonin metabolism in motorically asymptomatic R6/2 miceFanny Mochel, Brandon Durant, Alexandra Durr, et al.Cerebellum (London, England)|May 18, 2005
Spinocerebellar ataxia with mental retardation (SCA13)Giovanni Stevanin, Alexandra Durr, Nawal Benammar, et al.Current Opinion in Neurology|May 31, 2018
Hereditary ataxias and paraparesias: clinical and genetic updateLivia Parodi, Giulia Coarelli, Giovanni Stevanin, et al.Pageof 33