Evaluating the role of TMEM230 variants in Parkinson's disease by Baumann, Hauke, Wolff, Simone, Münchau, Alexander, Hagenah, Johann M, Lohmann, Katja, Klein, Christine

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Substantia nigra hyperechogenicity correlates with clinical status and number of Parkin mutated alleles by HAGENAH, Johann M, KÖNIG, Inke R, BECKER, Björn, HILKER, Rüdiger, KASTEN, Meike, HEDRICH, Katja, PRAMSTALLER, Peter P, KLEIN, Christine, SEIDEL, Günter

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Focal dystonia as a presenting sign of spinocerebellar ataxia 17 by Hagenah, Johann M., Zühlke, Christine, Hellenbroich, Yorck, Heide, Wolfgang, Klein, Christine

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Variation in the Uric Acid Transporter Gene SLC2A9 and Its Association with AAO of Parkinson’s Disease by Facheris, Maurizio F., Hicks, Andrew A., Minelli, Cosetta, Hagenah, Johann M., Kostic, Vladimir, Campbell, Susan, Hayward, Caroline, Volpato, Claudia B., Pattaro, Cristian, Vitart, Veronique, Wright, Alan, Campbell, Harry, Klein, Christine, Pramstaller, Peter P.

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Phenotypic spectrum of PINK1-associated parkinsonism in 15 mutation carriers from 1 family by Hiller, Anja, Hagenah, Johann M., Djarmati, Ana, Hedrich, Katja, Reetz, Kathrin, Schneider-Gold, Christiane, Kress, Wolfgang, Münchau, Alexander, Klein, Christine

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Effects of amantadine treatment on in vitro production of interleukin-2 in de-novo patients with idiopathic Parkinson's disease by Wandinger, Klaus P, Hagenah, Johann M, Klüter, Harald, Rothermundt, Matthias, Peters, Marion, Vieregge, Peter

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Mutations in THAP1 ( DYT6 ) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study by Djarmati, Ana, PhD, Schneider, Susanne A, MD, Lohmann, Katja, PhD, Winkler, Susen, BSc, Pawlack, Heike, BSc, Hagenah, Johann, MD, Brüggemann, Norbert, MD, Zittel, Simone, MD, Fuchs, Tania, PhD, Raković, Aleksandar, MSc, Schmidt, Alexander, MD, Jabusch, Hans-Christian, MD, Wilcox, Robert, MD, Kostić, Vladimir S, MD, Siebner, Hartwig, MD, Altenmüller, Eckart, MD, Münchau, Alexander, MD, Ozelius, Laurie J, PhD, Klein, Christine, MD

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Altered resting state brain networks in Parkinson's disease by Göttlich, Martin, Münte, Thomas F, Heldmann, Marcus, Kasten, Meike, Hagenah, Johann, Krämer, Ulrike M

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Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene by Lohmann, Katja, Wilcox, Robert A., Winkler, Susen, Ramirez, Alfredo, Rakovic, Aleksandar, Park, Jin-Sung, Arns, Björn, Lohnau, Thora, Groen, Justus, Kasten, Meike, Brüggemann, Norbert, Hagenah, Johann, Schmidt, Alexander, Kaiser, Frank J., Kumar, Kishore R., Zschiedrich, Katja, Alvarez-Fischer, Daniel, Altenmüller, Eckart, Ferbert, Andreas, Lang, Anthony E., Münchau, Alexander, Kostic, Vladimir, Simonyan, Kristina, Agzarian, Marc, Ozelius, Laurie J., Langeveld, Antonius P. M., Sue, Carolyn M., Tijssen, Marina A. J., Klein, Christine

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Gaucher disease ascertained through a Parkinson's center: Imaging and clinical characterization by Saunders-Pullman, Rachel, Hagenah, Johann, Dhawan, Vijay, Stanley, Kaili, Pastores, Gregory, Sathe, Swati, Tagliati, Michele, Condefer, Kelly, Palmese, Christina, Brüggemann, Norbert, Klein, Christine, Roe, AM, Kornreich, Ruth, Ozelius, Laurie, Bressman, Susan

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Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study by Ross, Owen A, Dr, Soto-Ortolaza, Alexandra I, BSc, Heckman, Michael G, MS, Aasly, Jan O, Prof, Abahuni, Nadine, MD, Annesi, Grazia, Prof, Bacon, Justin A, BSc, Bardien, Soraya, PhD, Bozi, Maria, MD, Brice, Alexis, Prof, Brighina, Laura, MD, Van Broeckhoven, Christine, Prof, Carr, Jonathan, Prof, Chartier-Harlin, Marie-Christine, Prof, Dardiotis, Efthimios, MD, Dickson, Dennis W, Prof, Diehl, Nancy N, BS, Elbaz, Alexis, Prof, Ferrarese, Carlo, Prof, Ferraris, Alessandro, MD, Fiske, Brian, PhD, Gibson, J Mark, Prof, Gibson, Rachel, PhD, Hadjigeorgiou, Georgios M, MD, Hattori, Nobutaka, Prof, Ioannidis, John PA, Prof, Jasinska-Myga, Barbara, MD, Jeon, Beom S, Prof, Kim, Yun Joong, Prof, Klein, Christine, Prof, Kruger, Rejko, MD, Kyratzi, Elli, MD, Lesage, Suzanne, PhD, Lin, Chin-Hsien, MD, Lynch, Timothy, Prof, Maraganore, Demetrius M, Prof, Mellick, George D, PhD, Mutez, Eugénie, MD, Nilsson, Christer, Prof, Opala, Grzegorz, Prof, Park, Sung Sup, Prof, Puschmann, Andreas, MD, Quattrone, Aldo, Prof, Sharma, Manu, PhD, Silburn, Peter A, Prof, Sohn, Young Ho, Prof, Stefanis, Leonidas, MD, Tadic, Vera, MD, Theuns, Jessie, PhD, Tomiyama, Hiroyuki, MD, Uitti, Ryan J, Prof, Valente, Enza Maria, Prof, van de Loo, Simone, PhD, Vassilatis, Demetrios K, PhD, Vilariño-Güell, Carles, PhD, White, Linda R, Prof, Wirdefeldt, Karin, MD, Wszolek, Zbigniew K, Prof, Wu, Ruey-Meei, Prof, Farrer, Matthew J, Prof

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Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson’s disease study by Westenberger, Ana, Usnich, Tatiana, Beetz, Christian, Vollstedt, Eva-Juliane, Laabs, Björn-Hergen, Gaber, Hanaa, Schell, Nathalie, Agarwal, Pinky, Aldred, Jason, Anderson, Roderick, Araújo, Rui, Arkadir, David, Avenali, Micol, Balal, Mehmet, Bhatia, Perminder, Bonello, Michael, Brauneis, Sarah, Cardoso, Francisco Eduardo Costa, Classen, Joseph, Coletta, Della, Crosiers, David, Cullufi, Paskal, Demirkiran, Meltem, de Carvalho Aguiar, Patricia, De Rosa, Anna, Djaldetti, Ruth, Dogu, Okan, Ellenbogen, Aaron, Ertan, Sibel, Fabiani, Giorgio, Fay-Karmon, Tsviya, Ferencz, Gerald J, Genç, Gençer, Gorospe, Arantza, Grandas, Francisco, Gruber, Doreen, Hanagasi, Hasmet A, Hassin-Baer, Sharon, Hauser, Robert A, Hernández-Vara, Jorge, Herting, Birgit, Hogg, Elliot, Hummelgen, Eduardo, Hussey, Kelly, Infante, Jon, Isaacson, Stuart H, Jauma, Serge, Kühn, Andrea, Litvan, Irene, López-Manzanares, Lydia, Luxmore, McKenzie, Manandhar, Sujeena, Marras, Connie, Morgan, John C, Mullin, Stephen, Musacchio, Thomas, Myers, Bennett, Negrotti, Anna, Nieves, Anette, Öztop-Çakmak, Özgür, Pal, Gian, Pavese, Nicola, Percesepe, Antonio, Piccoli, Tommaso, Pinto de Souza, Carolina, Prell, Tino, Reetz, Kathrin, Sammler, Esther, Santos-Lobato, Bruno Lopes, Saunders-Pullman, Rachel, Schofield, Christine M, Schumacher-Schuh, Artur F, Sesar, Ángel, Shafer, Stuart J, Silverdale, Monty, Sophia, Rani, Spitz, Mariana, Stocchi, Fabrizio, Tai, Yen F, Tönges, Lars, Toschi, Giulia, Urban, Peter Paul, Vandenberghe, Wim, Vela-Desojo, Lydia, Weill, Caroline, Weise, David, Wojcieszek, Joanne, Wolz, Martin, Yahalom, Gilad, Yalcin-Cakmakli, Gul, Kandaswamy, Krishna K, Balck, Alexander, Hanssen, Henrike, Borsche, Max, Lange, Lara M, Csoti, Ilona, Lohmann, Katja, Kasten, Meike, Rolfs, Arndt, Bauer, Peter

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Mechanical Behavior of Highly-Flexible Elastomeric Composites with Knitted-Fabric Reinforcement by Bekisli, Burak, Nied, Herman F., Pancrace, Johann

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A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease by 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

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NR4A2 mutations are rare among European patients with familial Parkinson's disease by Wellenbrock, Claudia, Hedrich, Katja, Schäfer, Nora, Kasten, Meike, Jacobs, Helfried, Schwinger, Eberhard, Hagenah, Johann, Pramstaller, Peter P., Vieregge, Peter, Klein, Christine

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Clinical and genetic features of myoclonus-dystonia in 3 cases: A video presentation by Kock, Norman, Kasten, Meike, Schüle, Birgitt, Hedrich, Katja, Wiegers, Karin, Kabakci, Kemal, Hagenah, Johann, Pramstaller, Peter P., Nitschke, Matthias F., Münchau, Alexander, Sperner, Jürgen, Klein, Christine

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