Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson disease by Barrett, M.J, Hagenah, J, Dhawan, V, Peng, S, Stanley, K, Raymond, D, Deik, A, Gross, S.J, Schreiber-Agus, N, Mirelman, A, Marder, K, Ozelius, L.J, Eidelberg, D, Bressman, S.B, Saunders-Pullman, R

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Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystonia by Walter, M, Bonin, M, Pullman, R. Saunders, Valente, E.M, Loi, M, Gambarin, M, Raymond, D, Tinazzi, M, Kamm, C, Glöckle, N, Poths, S, Gasser, T, Bressman, S.B, Klein, C, Ozelius, L.J, Riess, O, Grundmann, K

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1.261 THAP1/DYT6 SEQUENCE VARIANTS IN NON-DYT1 EARLY ONSET PRIMARY DYSTONIA IN CHINA AND THEIR EFFECTS ON RNA EXPRESSION by Cheng, F.B, Ozelius, L.J, Wan, X.H, Feng, J.C, Ma, L.Y, Wang, L, Yang, Y.M

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P1.070 Mutations in the THAP1 (DYT6) gene - a cause of generalized dystonia with prominent spasmodic dysphonia by Schneider, S.A, Djarmati, A, Lohmann, K, Winkler, S, Pawlack, H, Hagenah, J, Brüggemann, N, Zittel, S, Fuchs, T, Raković, A, Schmidt, A, Jabusch, H.-C, Wilcox, R, Kostić, V.S, Siebner, H, Münchau, A, Ozelius, L.J, Klein, C

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Gender differences in the risk of familial parkinsonism: Beyond LRRK2? by Saunders-Pullman, R., Stanley, K., Luciano, M. San, Barrett, M.J., Shanker, V., Raymond, D., Ozelius, L.J., Bressman, S.B.

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Genetik der Dystonien by Klein, Ch, Kann, M., Kis, B., Pramstaller, P.P., Breakefield, X.O., Ozelius, L.J., Vieregge, P.

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