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Journal of Neurology|April 12, 2015
Genetic landscape remodelling in spinocerebellar ataxias: the influence of next-generation sequencingMarie Coutelier, Giovanni Stevanin, Alexis Brice
Physiological Reviews|October 21, 2011
What genetics tells us about the causes and mechanisms of Parkinson's diseaseOlga Corti, Suzanne Lesage, Alexis Brice
Current Neurology and Neuroscience Reports|June 11, 2008
Recent advances in the genetics of spastic paraplegiasGiovanni Stevanin, Merle Ruberg, Alexis Brice
F1000Research|November 27, 2018
Recent advances in understanding dominant spinocerebellar ataxias from clinical and genetic points of viewGiulia Coarelli, Alexis Brice, Alexandra Durr
Current Opinion in Neurobiology|November 18, 2025
The genetics of autosomal recessive early-onset Parkinson's diseaseGuillaume Cogan, Suzanne Lesage, Alexis Brice
Journal of Neural Transmission. Supplementum|April 24, 2010
Neurodegeneration in Parkinson's disease: genetics enlightens physiopathologyOlga Corti, Margot Fournier, Alexis Brice
Current Neurology and Neuroscience Reports|September 1, 2005
New autosomal recessive cerebellar ataxias with oculomotor apraxiaIsabelle Le Ber, Alexis Brice, Alexandra Dürr
Current Opinion in Neurology|November 10, 2007
Hereditary spastic paraplegias: an updateChristel Depienne, Giovanni Stevanin, Alexis Brice, et al.
Cerebellum (London, England)|May 18, 2005
Spinocerebellar ataxia with mental retardation (SCA13)Giovanni Stevanin, Alexandra Durr, Nawal Benammar, et al.
Parkinsonism & Related Disorders|June 7, 2011
Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson's diseaseSoraya Bardien, Suzanne Lesage, Alexis Brice, et al.
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