Roussel, Martine

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

Moss, D. J. H., Pardiñas, A. F., Langbehn, D., Lo, K., Leavitt, B. R., Roos, R., Durr, A., Mead, S., Coleman, A., Santos, R. D., et al. (2017) · The Lancet Neurology

Genetic Neurodegenerative DiseasesGenetic Associations and Epidemiology

Cited by 312

Dysexecutive syndrome: diagnostic criteria and validation study

Godefroy, O., Azouvi, P., Robert, P., Roussel, M., LeGall, D., Meulemans, T., & Behalf of the Groupe de Réflexion sur l'Evaluation des Fonctions Exécutives Study Group (2010) · Annals of Neurology

Historical and Modern Theater StudiesCognitive Functions and Memory

Cited by 293

Cognitive Impairment and Dementia After Intracerebral Hemorrhage: A Cross-sectional Study of a Hospital-based Series

Garcia, P. Y., Roussel, M., Bugnicourt, J. M., Lamy, C., Canaple, S., Peltier, J., Loas, G., Deramond, H., & Godefroy, O. (2013) · Journal of Stroke and Cerebrovascular Diseases

Intracerebral and Subarachnoid Hemorrhage ResearchDementia and Cognitive Impairment Research

Cited by 96