Transcranial sonography findings in a large family with homozygous and heterozygous PINK1 mutations von Hagenah, J M, Becker, B, Brüggemann, N, Djarmati, A, Lohmann, K, Sprenger, A, Klein, C, Seidel, G

Volltext

Myoclonus-dystonia: significance of large SGCE deletions von Grünewald, A, Djarmati, A, Lohmann-Hedrich, K, Farrell, K, Zeller, J.A, Allert, N, Papengut, F, Petersen, B, Fung, V, Sue, C.M, O'Sullivan, D, Mahant, N, Kupsch, A, Chuang, R.S, Wiegers, K, Pawlack, H, Hagenah, J, Ozelius, L.J, Stephani, U, Schuit, R, Lang, A.E, Volkmann, J, Münchau, A, Klein, C

Volltext

DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease von HEDRICH, K, DJARMATI, A, BONIFATI, V, SCHWINGER, E, LANG, A. E, NOTH, J, BRESSMAN, S. B, PRAMSTALLER, P. P, RIESS, O, KLEIN, C, SCHÄFER, N, HERING, R, WELLENBROCK, C, WEISS, P. H, HILKER, R, VIEREGGE, P, OZELIUS, L. J, HEUTINK, P

Volltext

Evidence for linkage of restless legs syndrome to chromosome 9p : Are there two distinct loci? von LOHMANN-HEDRICH, K, NEUMANN, A, ZIEGLER, A, STEPHANI, U, KLEIN, C, KLEENSANG, A, LOHNAU, T, MUHLE, H, DJARMATI, A, KÖNIG, I. R, PRAMSTALLER, P. P, SCHWINGER, E, KRAMER, P. L

Volltext

A novel DCC mutation and genetic heterogeneity in congenital mirror movements von Djarmati-Westenberger, A, Brüggemann, N, Espay, A J, Bhatia, K P, Klein, C

Volltext

Large-scale assessment of polyglutamine repeat expansions in Parkinson disease von Wang, Lisa, Aasly, Jan O, Annesi, Grazia, Bardien, Soraya, Bozi, Maria, Brice, Alexis, Carr, Jonathan, Chung, Sun J, Clarke, Carl, Crosiers, David, Deutschländer, Angela, Eckstein, Gertrud, Farrer, Matthew J, Goldwurm, Stefano, Garraux, Gaetan, Hadjigeorgiou, Georgios M, Hicks, Andrew A, Hattori, Nobutaka, Klein, Christine, Jeon, Beom, Kim, Yun J, Lesage, Suzanne, Lin, Juei-Jueng, Lynch, Timothy, Lichtner, Peter, Lang, Anthony E, Mok, Vincent, Jasinska-Myga, Barbara, Mellick, George D, Morrison, Karen E, Opala, Grzegorz, Pihlstrøm, Lasse, Pramstaller, Peter P, Park, Sung S, Quattrone, Aldo, Rogaeva, Ekaterina, Ross, Owen A, Stefanis, Leonidas, Stockton, Joanne D, Silburn, Peter A, Theuns, Jessie, Tan, Eng K, Tomiyama, Hiroyuki, Toft, Mathias, Van Broeckhoven, Christine, Uitti, Ryan J, Wirdefeldt, Karin, Wszolek, Zbigniew, Xiromerisiou, Georgia, Yueh, Kuo-Chu, Zhao, Yi, Gasser, Thomas, Maraganore, Demetrius M, Krüger, Rejko, Sharma, Manu

Volltext

A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease von Krüger, Rejko, Sharma, Manu, Riess, Olaf, Gasser, Thomas, Van Broeckhoven, Christine, Theuns, Jessie, Aasly, Jan, Annesi, Grazia, Bentivoglio, Anna Rita, Brice, Alexis, Djarmati, Ana, Elbaz, Alexis, Farrer, Matthew, Ferrarese, Carlo, Gibson, J. Mark, Hadjigeorgiou, Georgios M, Hattori, Nobutaka, Ioannidis, John P.A, Jasinska-Myga, Barbara, Klein, Christine, Lambert, Jean-Charles, Lesage, Suzanne, Lin, Juei-Jueng, Lynch, Timothy, Mellick, George D, de Nigris, Francesa, Opala, Grzegorz, Prigione, Alessandro, Quattrone, Aldo, Ross, Owen A, Satake, Wataru, Silburn, Peter A, Tan, Eng King, Toda, Tatsushi, Tomiyama, Hiroyuki, Wirdefeldt, Karin, Wszolek, Zbigniew, Xiromerisiou, Georgia, Maraganore, Demetrius M

Volltext

MECP2 mutations in Serbian Rett syndrome patients von Djarmati, A., Dobričić, V., Kecmanović, M., Marsh, P., Jančić-Stefanović, J., Klein, C., Djurić, M., Romac, S.

Volltext

P1.070 Mutations in the THAP1 (DYT6) gene - a cause of generalized dystonia with prominent spasmodic dysphonia von 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

Volltext

SCA2 and SCA3 mutations in young-onset dopa-responsive parkinsonism von Svetel, M., Djarmati, A., Dragašević, N., Savić, D., Čuljković, B., Romac, S., Kostić, V. S.

Volltext

α-Synuclein gene duplication is present in sporadic Parkinson disease von Brueggemann, N., Odin, P., Gruenewald, A., Tadic, V., Hagenah, J., Seidel, G., Lohmann, K., Klein, C., Djarmati, A.

Volltext

PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism von Klein, Christine, Djarmati, Ana, Hedrich, Katja, Schäfer, Nora, Scaglione, Cesa, Marchese, Roberta, Kock, Norman, Schüle, Birgitt, Hiller, Anja, Lohnau, Thora, Winkler, Susen, Wiegers, Karin, Hering, Robert, Bauer, Peter, Riess, Olaf, Abbruzzese, Giovanni, Martinelli, Paolo, Pramstaller, Peter P

Volltext

Co-occurrence of affective and schizophrenia spectrum disorders with PINK1 mutations von Steinlechner, Susanne, Stahlberg, Jessica, Völkel, Birgit, Djarmati, Ana, Hagenah, Johann, Hiller, Anja, Hedrich, Katja, König, Inke, Klein, Christine, Lencer, Rebekka

Volltext

Spinocerebellar ataxia type 17 in the Yugoslav population von Alendar, A., Čuljković, B., Savić, D., Djarmati, A., Keckarević, M., Ristić, A., Dragašević, N., Kosić, V., Romac, S.

Volltext

Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: Large-scale collaborative study von Evangelou, Evangelos, Maraganore, Demetrius M., Annesi, Grazia, Brighina, Laura, Brice, Alexis, Elbaz, Alexis, Ferrarese, Carlo, Hadjigeorgiou, Georgios M., Krueger, Rejko, Lambert, Jean-Charles, Lesage, Suzanne, Markopoulou, Katerina, Mellick, George D., Meeus, Bram, Pedersen, Nancy L., Quattrone, Aldo, Van Broeckhoven, Christine, Sharma, Manu, Silburn, Peter A., Tan, Eng-King, Wirdefeldt, Karin, Ioannidis, John P.A.

Volltext

Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients von Djarmati, Ana, Hedrich, Katja, Svetel, Marina, Schäfer, Nora, Juric, Vladislava, Vukosavic, Slobodanka, Hering, Robert, Riess, Olaf, Romac, Stanka, Klein, Christine, Kostic, Vladimir

Volltext

Co-occurrence of restless legs syndrome and Parkin mutations in two families von Adel, Susanna, Djarmati, Ana, Kabakci, Kemal, Pichler, Irene, Eskelson, Cordula, Lohnau, Thora, Kock, Norman, Hagenah, Johann, Hedrich, Katja, Schwinger, Eberhard, Kramer, Patricia L., Pramstaller, Peter P., Klein, Christine

Volltext

Chemical composition of leaf extracts of Stevia rebaudiana Bertoni grown experimentally in Vojvodina von Markovic, Ivana, Djarmati, Zoltan, Abramovic, Biljana

Volltext

Transcranial sonography findings in a large family with homozygous and heterozygous PINK1 mutations von HAGENAH, J. M, BECKER, B, BRÜGGEMANN, N, DJARMATI, A, LOHMANN, K, SPRENGER, A, KLEIN, C, SEIDEL, G

Volltext

Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease von Rakovic, A, Stiller, B, Djarmati, A, Flaquer, A, Freudenberg, J, Toliat, M R, Linnebank, M, Kostic, V, Lohmann, K, Paus, S, Nürnberg, P, Kubisch, C, Klein, C, Wüllner, U, Ramirez, A

Volltext