The brain and the muscles of genetics von Anheim, M

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Triple-gene therapy in Parkinson disease (ProSavin): toward a putaminal dopamine factory? von Anheim, M

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Deep intronic FGF14 GAA-repeat expansion in late-onset cerebellar ataxia: Last but not least von Anheim, M.

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Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers von ANHEIM, M, ELBAZ, A, LESAGE, S, DURR, A, CONDROYER, C, VIALLET, F, POLLAK, P, BONAÏTI, B, BONAÏTI-PELLIE, C, BRICE, A

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Neurology and pregnancy: The delivery von Anheim, M.

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Journées d’enseignement supérieur de neurologie, Strasbourg 2022 von Anheim, M.

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Movement disorders in mitochondrial diseases von Tranchant, C., Anheim, M.

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Brain MRI of multiple system atrophy of cerebellar type: a prospective study with implications for diagnosis criteria von Carré, G., Dietemann, J. L., Gebus, O., Montaut, S., Lagha-Boukbiza, O., Wirth, T., Kremer, S., Namer, I. J., Anheim, M., Tranchant, C.

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CANVAS: A very late onset cerebellar ataxia, due to biallelic expansions in the RFC1 gene von Tranchant, C., Anheim, M.

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Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients von Anheim, M., Monga, B., Fleury, M., Charles, P., Barbot, C., Salih, M., Delaunoy, J. P., Fritsch, M., Arning, L., Synofzik, M., Schöls, L., Sequeiros, J., Goizet, C., Marelli, C., Le Ber, I., Koht, J., Gazulla, J., De Bleecker, J., Mukhtar, M., Drouot, N., Ali-Pacha, L., Benhassine, T., Chbicheb, M., M’Zahem, A., Hamri, A., Chabrol, B., Pouget, J., Murphy, R., Watanabe, M., Coutinho, P., Tazir, M., Durr, A., Brice, A., Tranchant, C., Koenig, M.

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Unravelling the etiology of sporadic late-onset cerebellar ataxia in a cohort of 205 patients: a prospective study von Bogdan, T., Wirth, T., Iosif, A., Schalk, A., Montaut, S., Bonnard, C., Carre, G., Lagha-Boukbiza, O., Reschwein, C., Albugues, E., Demuth, S., Landsberger, H., Einsiedler, M., Parratte, T., Nguyen, A., Lamy, F., Durand, H., Fahrer, P., Voulleminot, P., Bigaut, K., Chanson, J. B., Nicolas, G., Chelly, J., Cazeneuve, C., Koenig, M., Bund, C., Namer, I. J., Kremer, S., Calmels, N., Tranchant, C., Anheim, M.

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Novel anoctamin-3 missense mutation responsible for early-onset myoclonic dystonia von Delamarre, A., Chelly, J., Guehl, D., Drouot, N., Tranchant, C., Anheim, M., Burbaud, P.

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Neuropathies périphériques associées aux ataxies cérébelleuses héréditaires von Anheim, M., Tranchant, C.

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Autosomal recessive cerebellar ataxias von Anheim, M

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Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population von SAAD, Mohamad, LESAGE, Suzanne, POLLAK, Pierre, DAMIER, Philippe, TISON, François, SILBURN, Peter A, TZOURIO, Christophe, FORIANI, Sylvie, LORIOT, Marie-Anne, GIROUD, Maurice, HELMER, Catherine, PORTET, Florence, SAINT-PIERRE, Aude, AMOUYEL, Philippe, LATHROP, Mark, ELBAZ, Alexis, DURR, Alexandra, MARTINEZ, Maria, BRICE, Alexis, CORVOL, Jean-Christophe, ZELENIKA, Diana, LAMBERT, Jean-Charles, VIDAILHET, Marie, MELLICK, George D, LOHMANN, Ebba, DURIF, Franck

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Early hyperdopaminergic state following sub-thalamic nucleus deep brain stimulation in Parkinson disease von Lamy, F., Lagha-Boukbiza, O., Wirth, T., Philipps, C., Longato, N., Gebus, O., Montaut, S., Mengin, A., Voirin, J., Proust, F., Tuzin, N., Anheim, M., Tranchant, C.

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Severe early-onset impulsive compulsive behavior and psychosis in PLA2G6-related juvenile Parkinson's disease von Wirth, T., Weibel, S., Montaut, S., Bigaut, K., Rudolf, G., Chelly, J., Tranchant, C., Anheim, M.

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Le cerveau et les muscles de la génétique von Anheim, M.

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Paroxysmal dyskinesia: When a PRRT2 variant hides a curable cause von Schneider, V., Ferrari-Henquinet, M., Diallo, A.O., Chelly, J., Anheim, M., Tranchant, C.

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French guidelines for the diagnosis and management of Tourette syndrome von Hartmann, A., Ansquer, S., Brefel-Courbon, C., Burbaud, P., Castrioto, A., Czernecki, V., Damier, P., Deniau, E., Drapier, S., Jalenques, I., Marechal, O., Priou, T., Spodenkiewicz, M., Thobois, S., Roubertie, A., Witjas, T., Anheim, M.

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