M05 Registry in Europe; study sites' catchment area based on participant flow von Koivisto, S Pro, da Silva, W Vieira

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M05Registry in Europe; study sites' catchment area based on participant flow von Koivisto, S Pro, da Silva, W Vieira

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Suicidal ideation in a European Huntington's disease population von Hubers, Anna A.M, van Duijn, Erik, Roos, Raymund A.C, Craufurd, David, Rickards, Hugh, Bernhard Landwehrmeyer, G, van der Mast, Rose C, Giltay, Erik J

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Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease von AZIZ, N. A, JURGENS, C. K, LANDWEHRMEYER, G. B, VAN ROON-MOM, W. M. C, VAN OMMEN, G. J. B, STIJNEN, T, ROOS, R. A. C

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NMDA receptor gene variations as modifiers in Huntington disease: a replication study von Saft, Carsten, Epplen, Jörg T, Wieczorek, Stefan, Landwehrmeyer, G Bernhard, Roos, Raymund A C, de Yebenes, Justo Garcia, Dose, Matthias, Tabrizi, Sarah J, Craufurd, David, Arning, Larissa

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Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study von Moss, Davina J Hensman, MBBS, Pardiñas, Antonio F, PhD, Langbehn, Douglas, Prof, Lo, Kitty, PhD, Leavitt, Blair R, Prof, Roos, Raymund, Prof, Durr, Alexandra, Prof, Mead, Simon, Prof, Holmans, Peter, Prof, Jones, Lesley, Prof, Tabrizi, Sarah J, Prof

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Clinical manifestations of intermediate allele carriers in Huntington disease von Cubo, Esther, Ramos-Arroyo, María A, Martinez-Horta, Saul, Martínez-Descalls, Asunción, Calvo, Sara, Gil-Polo, Cecilia

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Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY von Orth, Michael

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Discrepancies in reporting the CAG repeat lengths for Huntington's disease von QUARRELL, Oliver W, HANDLEY, Olivia, O'DONOVAN, Kirsty, DUMOULIN, Christine, RAMOS-ARROYO, Maria, BIUNNO, Ida, BAUER, Peter, KLINE, Margaret, BERNHARD LANDWEHRMEYER, G

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Clinical and genetic characteristics of late-onset Huntington's disease von Oosterloo, Mayke, Bijlsma, Emilia K., van Kuijk, Sander MJ, Minkels, Floor, de Die-Smulders, Christine EM

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The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients von Metzger, Silke, Walter, Carolin, Riess, Olaf, Roos, Raymund A C, Nielsen, Jørgen E, Craufurd, David, Nguyen, Huu Phuc

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Identification of symbol digit modality test score extremes in Huntington's disease von Braisch, Ulrike, Muche, Rainer, Rothenbacher, Dietrich, Landwehrmeyer, Georg Bernhard, Long, Jeffrey D, Orth, Michael, Bachoud-Levi, Anne-Catherine, Bentivoglio, Anna-Rita, Biunno, Ida, Bonelli, Raphael M, Burgunder, Jean-Marc, Dunnett, Stephen B, Ferreira, Joaquim J, Handley, Olivia J, Heiberg, Arvid, Illmann, Torsten, Landwehrmeyer, G. Bernhard, Levey, Jamie, Ramos-Arroyo, Maria, Nielsen, Jorgen E, Koivisto, Susana Pro, Paivarinta, Markku, Roos, Raymund A.C, Sebastian, Ana Rojo, Tabrizi, Sarah J, Vandenberghe, Wim, Verellen-Dumoulin, Christine, Uhrova, Tereza, Wahlstrom, Jan, Zaremba, Jacek, Baake, Verena, Barth, Katrin, Bos, Reineke, Come, Adrien, Guedes, Leonor Correia, Finisterra, Ana Maria, Garde, Monica Bascunana, Betz, Sabrina, Callaghan, Jenny, Capodarca, Selene, Wildson, Sebastien Charpentier, da Silva, Vieira, Di Renzo, Martina, Ecker, Daniel, Finisterra, Maria, Fullam, Ruth, Genoves, Camille, Gilling, Mette, Hvalstedt, Carina, Held, Christine, Koppers, Kerstin, Lamanna, Claudia, Laura, Matilde, Descals, Asuncion Martinez, Martinez-Horta, Saul, Mestre, Tiago, Minster, Sara, Monza, Daniela, Mutze, Lisanne, Oehmen, Martin, Padieu, Helene, Paterski, Laurent, Peppa, Nadia, Rindal, Beate, Roren, Niini, Sasinkova, Pavla, Seliverstov, Yury, Timewell, Erika, Townhill, Jenny, Cubillo, Patricia Trigo, van Walsem, Marleen R, Witjes-Ane, Marie-Noelle, Witkowski, Grzegorz, Wright, Abigail, Yudina, Elizaveta, Zielonka, Daniel, Zielonka, Eugeniusz, Zinzi, Paola, Braunwarth, Eva-Maria, Brugger, Florian, Buratti, Lisa, Hametner, Eva-Maria, Hepperger, Caroline, Holas, Christiane, Hotter, Anna, Hussl, Anna, Larcher, Barbara, Mahlknecht, Philipp, Muller, Christoph, Pinter, Bernadette, Poewe, Werner, Seppi, Klaus, Sprenger, Fabienne, Wenning, Gregor, Dupuis, Michel, Minet, Cecile, Ribai, Pascale, Van Paemel, Dominique, Klempir, Jiri, Majerova, Veronika

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Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study von Moss, Davina, Pardiñas, Antonio, Langbehn, Douglas, Lo, Kitty, Leavitt, Blair, Roos, Raymund, Durr, Alexandra, Mead, Simon, Holmans, Peter, Jones, Lesley, Tabrizi, Sarah, Coleman, A, Santos, R Dar, Decolongon, J, Sturrock, A, Bardinet, E, Ret, C Jauff, Justo, D, Lehericy, S, Marelli, C, Nigaud, K, Valabrègue, R, van den Bogaard, Sja, Dumas, E, van der Grond, J, t'Hart, Ep, Jurgens, C, Witjes-Ane, M-N, Arran, N, Callaghan, J, Stopford, C, Frost, C, Jones, R, Hobbs, N, Lahiri, N, Ordidge, R, Owen, G, Pepple, T, Read, J, Say, M, Wild, E, Patel, A, Fox, N, Gibbard, C, Malone, I, Crawford, H, Whitehead, D, Keenan, S, Cash, D, Berna, C, Bechtel, N, Bohlen, S, Man, a Hoff, Kraus, P, Axelson, E, Wang, C, Acharya, T, Lee, S, Monaco, W, Campbell, C, Queller, S, Whitlock, K, Campbell, M, Frajman, E, Milchman, C, O'Regan, A, Labuschagne, I, Stout, J, Landwehrmeyer, B, Craufurd, D, Scahill, R, Hicks, S, Kennard, C, Johnson, H, Tobin, A, Rosas, Hd, Reilmann, R, Borowsky, B, Pourchot, C, Andrews, S, Bachoud-Lévi, Anne-Catherine, Bentivoglio, Anna Rita, Biunno, Ida, Bonelli, Raphael, Burgunder, Jean-Marc, Dunnett, Stephen, Ferreira, Joaquim, Handley, Olivia, Heiberg, Arvid, Illmann, Torsten, Landwehrmeyer, G. Bernhard, Levey, Jamie, Ramos-Arroyo, Maria, Nielsen, Jørgen, Koivisto, Susana Pro, Päivärinta, Markku, Roos, Raymund A.C., Sebastián, a Rojo, Vandenberghe, Wim, Verellen-Dumoulin, Christine

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