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Biblio

3 resultats trouvés

Filtres: Auteur is Tesson, Christelle [Clear All Filters]

C

Roux T, Barbier M, Papin M, Davoine C-S, Sayah S, Coarelli G, Charles P, Marelli C, Parodi L, Tranchant C et al.. Submitted. Clinical, neuropathological, and genetic characterization ofSTUB1variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment. GENETICS IN MEDICINE.

Roux T, Barbier M, Papin M, Davoine C-S, Sayah S, Coarelli G, Charles P, Marelli C, Parodi L, Tranchant C et al.. Submitted. Clinical, neuropathological, and genetic characterization ofSTUB1variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment. GENETICS IN MEDICINE.

P

Coutelier M, Coarelli G, Monin M-L, Konop J, Davoine C-S, Tesson C, Valter R, Anheim M, Behin A, Castelnovo G et al.. 2017. A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies. BRAIN. 140:1579-1594.