Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutation

Por Anheim, M, Hannequin, D, Boulay, C, Martin, C, Campion, D, Tranchant, C
Publicado em 2007

Neurofibrillary tangles in Gerstmann-Sträussler-Scheinker syndrome with the A117V prion gene mutation

Por Tranchant, C, Sergeant, N, Wattez, A, Mohr, M, Warter, J, Delacourte, A
Publicado em 1997

Gerstmann-Sträussler-Scheinker disease in an Alsatian family: clinical and genetic studies.

Por Tranchant, C, Doh-ura, K, Warter, J M, Steinmetz, G, Chevalier, Y, Hanauer, A, Kitamoto, T, Tateishi, J
Publicado em 1992

Myopathy with tubular aggregates and gyrate atrophy of the choroid and retina due to hyperornithinaemia

Por Fleury, M, Barbier, R, Ziegler, F, Mohr, M, Caron, O, Dollfus, H, Tranchant, C, Warter, J M
Publicado em 2007

A randomized controlled double-blind study of rotigotine on neuropsychiatric symptoms in de novo PD

Por Castrioto, A., Thobois, S., Anheim, M., Quesada, J. L., Lhommée, E., Klinger, H., Bichon, A., Schmitt, E., Durif, F., Azulay, J. P., Houeto, J. L., Longato, N., Philipps, C., Pelissier, P., Broussolle, E., Moro, E., Tranchant, C., Fraix, V., Krack, P.
Publicado no NPJ Parkinsons Dis (2020)

Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes

Por du Montcel, S Tezenas, Clot, F, Vidailhet, M, Roze, E, Damier, P, Jedynak, C P, Camuzat, A, Lagueny, A, Vercueil, L, Doummar, D, Guyant‐Maréchal, L, Houeto, J‐L, Ponsot, G, Thobois, S, Cournelle, M‐A, Durr, A, Durif, F, Echenne, B, Hannequin, D, Tranchant, C, Brice, A
Publicado em 2006

Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein

Por Mariani, L. L., Rivaud-Péchoux, S., Charles, P., Ewenczyk, C., Meneret, A., Monga, B. B., Fleury, M.-C., Hainque, E., Maisonobe, T., Degos, B., Echaniz-Laguna, A., Renaud, M., Wirth, T., Grabli, D., Brice, A., Vidailhet, M., Stoppa-Lyonnet, D., Dubois-d’Enghien, C., Le Ber, I., Koenig, M., Roze, E., Tranchant, C., Durr, A., Gaymard, B., Anheim, M.
Publicado no Sci Rep (2017)