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Frontiers in Genetics|April 9, 2021
The History of Gene Hunting in Hereditary Spinocerebellar Degeneration: Lessons From the Past and Future PerspectivesAshraf Yahia, Giovanni StevaninJournal of Molecular Biology|March 8, 2020
Impairment of Lysosome Function and Autophagy in Rare Neurodegenerative DiseasesFrédéric Darios, Giovanni StevaninCerebellum (London, England)|April 18, 2008
Spinocerebellar ataxia 17 (SCA17) and Huntington's disease-like 4 (HDL4)Giovanni Stevanin, Alexis BriceHandbook of Clinical Neurology|August 11, 2011
Spinocerebellar ataxia 13 and 25Giovanni Stevanin, Alexandra DürrJournal of Neurology|April 12, 2015
Genetic landscape remodelling in spinocerebellar ataxias: the influence of next-generation sequencingMarie Coutelier, Giovanni Stevanin, Alexis BriceCurrent Neurology and Neuroscience Reports|June 11, 2008
Recent advances in the genetics of spastic paraplegiasGiovanni Stevanin, Merle Ruberg, Alexis BriceCurrent Neurology and Neuroscience Reports|March 2, 2019
Update on the Genetics of Spastic ParaplegiasMaxime Boutry, Sara Morais, Giovanni StevaninHuman Genetics|March 12, 2015
Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosologyChristelle Tesson, Jeanette Koht, Giovanni StevaninFrontiers in Neuroscience|March 18, 2020
Lipids in the Physiopathology of Hereditary Spastic ParaplegiasFrédéric Darios, Fanny Mochel, Giovanni StevaninCells|August 7, 2021
Current Knowledge of Endolysosomal and Autophagy Defects in Hereditary Spastic ParaplegiaLiriopé Toupenet Marchesi, Marion Leblanc, Giovanni StevaninPageof 19