Polymorphisms in the receptor for GDNF ( RET ) are not associated with Parkinson's disease in Southern Germany von Lücking, C.B, Lichtner, P, Kramer, E.R, Gieger, C, Illig, T, Dichgans, M, Berg, D, Gasser, T

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Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations von VAN DE WARRENBURG, B. P. C, LAMMENS, M, LÜCKING, C. B, DENEFLE, P, WESSELING, P, BOOIJ, J, PRAAMSTRA, P, QUINN, N, BRICE, A, HORSTINK, M. W. I. M

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Parkin interacts with the proteasome subunit α4 von Dächsel, J.C., Lücking, C.B., Deeg, S., Schultz, E., Lalowski, M., Casademunt, E., Corti, O., Hampe, C., Patenge, N., Vaupel, K., Yamamoto, A., Dichgans, M., Brice, A., Wanker, E.E., Kahle, P.J., Gasser, T.

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[18F]-dopa PET study in patients with juvenile-onset PD and parkin gene mutations von BROUSSOLLE, E, LÜCKING, C. B, GINOVART, N, POLLAK, P, REMY, P, DÜRR, A

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New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism von RAWAL, N, PERIQUET, M, HORSTINK, M. W. I. M, DOS SANTOS BELE, W, BROUSOLLE, E, DESTEE, A, MIZUNO, Y, FARRER, M, DELEUZE, J.-F, DE MICHELE, G, AGID, Y, DÜRR, A, LOHMANN, E, BRICE, A, LÜCKING, C. B, TEIVE, H. A, AMBROSIO, G, RASKIN, S, LINCOLN, S, HATTORI, N, GUIMARAES, J

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Mitochondrial NADH dehydrogenase and CYP2D6 genotypes in Lewy-body Parkinsonism von Kösel, S., Lücking, C.B., Egensperger, R., Mehraein, P., Graeber, M.B.

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Parkin modulates gene expression in control and ceramide-treated PC12 cells von Unschuld, P.G., Dächsel, J., Darios, F., Kohlmann, A., Casademunt, E., Lehmann-Horn, K., Dichgans, M., Ruberg, M., Brice, A., Gasser, T., Lücking, C.B.

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Parkin modulates gene expression in control and ceramide-treated PC12 cells von Unschuld, P.G., Dächsel, J., Darios, F., Kohlmann, A., Casademunt, E., Lehmann-Horn, K., Dichgans, M., Ruberg, M., Brice, A., Gasser, T., Lücking, C.B.

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Identifikation einer proteasomalen alpha-Untereinheit als neuen Parkin-Interaktor von Lücking, C.B, Dächsel, J.C, Deeg, S, Schultz, E, Corti, O, Hampe, C, Patenge, N, Yamamoto, A, Dichgans, M, Brice, A, Kahle, P.J, Wanker, E.E, Gasser, T

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Absence of the Mitochondrial A7237T Mutation in Parkinson′s Disease von Lucking, C.B., Kosel, S., Mehraein, P., Graeber, M.B.

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Strigula lacinulata Vain

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