Scale for the assessment and rating of ataxia : Development of a new clinical scale von SCHMITZ-HÜBSCH, T, TEZENAS DU MONTCEL, S, KREMER, B, MARIOTTI, C, MELEGH, B, PANDOLFO, M, RAKOWICZ, M, RIBAI, P, ROLA, R, SCHOLS, L, SZYMANSKI, S, VAN DE WARRENBURG, B. P, BALIKO, L, DÜRR, A, KLOCKGETHER, T, BERCIANO, J, BOESCH, S, DEPONDT, C, GIUNTI, P, GLOBAS, C, INFANTE, J, KANG, J.-S

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Spinocerebellar ataxia types 1, 2, 3, and 6 : Disease severity and nonataxia symptoms von SCHMITZ-HÜBSCH, T, COUDERT, M, RIBAI, P, SZYMANSKI, S, INFANTE, J, VAN DE WARRENBURG, B. P. C, DÜRR, A, TIMMANN, D, BOESCH, S, FANCELLU, R, ROLA, R, DEPONDT, C, BAUER, P, SCHÖLS, L, ZDIENICKA, E, KANG, J.-S, DÖHLINGER, S, KREMER, B, STEPHENSON, D. A, MELEGH, B, PANDOLFO, M, DI DONATO, S, TEZENAS DU MONTCEL, S, GIUNTI, P, KLOCKGETHER, T, GLOBAS, C, BALIKO, L, FILLA, A, MARIOTTI, C, RAKOWICZ, M, CHARLES, P

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Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia von Depienne, Christel, Fedirko, Estelle, Forlani, Sylvie, Cazeneuve, Cécile, Ribaï, Pascale, Feki, Imed, Tallaksen, Chantal, Nguyen, Karine, Stankoff, Bruno, Ruberg, Merle, Stevanin, Giovanni, Durr, Alexandra, Brice, Alexis

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SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years von Namekawa, M, Ribai, P, Nelson, I, Forlani, S, Fellmann, F, Goizet, C, Depienne, C, Stevanin, G, Ruberg, M, Dürr, A, Brice, A

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A new phenotype linked to SPG27 and refinement of the critical region on chromosome von Ribai, Pascale, Stevanin, Giovanni, Bouslam, Naima, Pontier, Bénédicte, Nelson, Isabelle, Fontaine, Bertrand, Dussert, Christel, Charon, Céline, Durr, Alexandra, Brice, Alexis

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Acute Balint's syndrome is not always caused by a stroke von Ribai, P., Vokaer, M., De Tiège, X., Massat, I., Slama, H., Bier, J.C.

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Usefulness of prolonged video-EEG monitoring and provocative procedure with saline injection for the diagnosis of non epileptic seizures of psychogenic origin von RIBAÏ, Pascale, TUGENDHAFT, Patrick, LEGROS, Benjamin

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A novel locus for autosomal dominant uncomplicated hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3 von HANEIN, Sylvain, DÜRR, Alexandra, BRICE, Alexis, STEVANIN, Giovanni, RIBAI, Pascale, FORLANI, Sylvie, LEUTENEGGER, Anne-Louise, NELSON, Isabelle, BABRON, Marie-Claude, ELLEUCH, Nizar, DEPIENNE, Christel, CHARON, Céline

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A new phenotype linked to SPG27 and refinement of the critical region on chromosome 10 von RIBAI, Pascale, STEVANIN, Giovanni, BOUSLAM, Naima, PONTIER, Bénédicte, NELSON, Isabelle, FONTAINE, Bertrand, DUSSERT, Christel, CHARON, Céline, DURR, Alexandra, BRICE, Alexis

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Self-rated health status in spinocerebellar ataxia--results from a European multicenter study von Schmitz-Hübsch, T, Coudert, M, Giunti, P, Globas, C, Baliko, L, Fancellu, R, Mariotti, C, Filla, A, Rakowicz, M, Charles, P, Ribai, P, Szymanski, S, Infante, J, van de Warrenburg, B P, Dürr, A, Timmann, D, Boesch, S, Rola, R, Depondt, C, Schöls, L, Zdzienicka, E, Kang, J S, Ratzka, S, Kremer, B, Schulz, J B, Klopstock, T, Melegh, B, du Montcel, S T, Klockgether, T

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Congenital stationary night blindness: Report of an autosomal recessive family and linkage analysis von Abramowicz, Marc J., Ribai, Pascale, Cordonnier, Monique

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A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A gene von Namekawa, Michito, Nelson, Isabelle, Ribai, Pascale, Dürr, Alexandra, Denis, Elodie, Stevanin, Giovanni, Ruberg, Merle, Brice, Alexis

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The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease von METZGER, Silke, BAIUER, Peter, MELEGH, Bela, HAVASI, Victoria, BALIKO, Lazlo, WIECZOREK, Stefan, ARNING, Larissa, ZAREMBA, Jacek, SUIEK, Anna, HOFFMAN-ZACHARSKA, Dorota, BASAK, A. Nazli, ERSOY, Nagehan, TOMIUK, Juergen, ZIDOVSKA, Jana, KEBRDLOVA, Vera, PANDOLFO, Massimo, RIBAÏ, Pascale, KADASI, Ludovit, KVASNICOVA, Marta, WEBER, Bernhard H. F, KREUZ, Friedmar, DOSE, Matthias, STUHRMANN, Manfred, LACCONE, Franco, RIESS, Olaf, DIDONATO, Stefano, GELLERA, Cinzia, SOLIVERI, Paola, LANGE, Herwig W, WEIRICH-SCHWAIGER, Helga, WENNING, Gregor K

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Transient cerebral arteriopathy in infancy associated with enteroviral infection von RibaI, Pascale, Liesnard, Corinne, Rodesch, Georges, Giurgea, Sanda, Verheulpen, Denis, David, Philippe, Van Bogaert, Patrick

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SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years von NAMEKAWA, M, RIBAI, P, BRICE, A, NELSON, I, FORLANI, S, FELLMANN, F, GOIZET, C, DEPIENNE, C, STEVANIN, G, RUBERG, M, DÜRR, A

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Sialic acid residues in the labial salivary glands from Sjögren's syndrome patients von PENALOZA, A, DECAESTECKER, C, RIBAÏ, P, NAGY, N, SALMON, I, APPELBOOM, T, DANGUY, A, KISS, R, STEINFELD, S

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Brachial plexus neuritis: is prognosis worse in children? von Verheulpen, Denis, Ribaı̈, Pascale, Gérard, Jean-Marie, Caroyer, Jean-Marc, Van Bogaert, Patrick

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Genetic analysis of candidate genes modifying the age-at-onset in Huntington's Disease: results of a large European association study von Metzger, S, Bauer, P, Tomiuk, J, Laccone, F, DiDonato, S, Gellera, C, Lange, H.W, Weirich-Schwaiger, H, Melegh, B, Havasi, V, Baliko, L, Epplen, J.T, Zaremba, J, Sulek, A, Basak, A.N, Soydan, E, Zidovska, J, Kebrdlova, V, Pandolfo, M, Ribai, P, Kadasi, L, Kvasnicova, M, Weber, B.H.F, Kreuz, F, Dose, M, Stuhrmann, M, Riess, O

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Acute Balint's syndrome is not always caused by a stroke von Ribai, P, Vokaer, M, De Tiège, X, Massat, I, Slama, H, Bier, J C

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Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study von McNulty, P, Pilcher, R, Ramesh, R, Necuiniate, R, Hughes, A, Farewell, D, Holmans, P, Jones, L, Bonelli, RM, Hecht, K, Herranhof, B, Holl, A, Kapfhammer, HP, Koppitz, M, Lilek, S, Magnet, M, Müller, N, Otti, D, Painold, A, Reisinger, K, Scheibl, M, Schöggl, H, Ullah, J, Braunwarth, EM, Brugger, F, Buratti, L, Hametner, EM, Hepperger, C, Holas, C, Hotter, A, Hussl, A, Larcher, B, Mahlknecht, P, Müller, C, Pinter, B, Poewe, W, Reiter, EM, Seppi, K, Sprenger, F, Wenning, G, Ladurner, G, Sinadinosa, D, Staffen, W, Walleczek, AM, Constant, E, Gillardin, AF, Léonard, MC, Verellen-Dumoulin, C, Van De Wyngaerde, F, Dupuis, M, Minet, C, Ribaï, P, Van Paemel, D, Boogaerts, A, Vandenberghe, W, Van Reijen, D, Kaiserova, M, Šenkárová, Z, Klempíř, J, Majerová, V, Roth, J, Madsen, LH, Møller, AT, Hjermind, L, Jacobsen, O, Lindquist, S, Nielsen, J, Regeur, L, Stockholm, J, Larsen, IU, Vangsted-Hansen, C, Vinther-Jensen, T, Lolk, A, Lundsgaard, M, Wermuth, L, Andersson, C, Nyberg, C, Sundblom, J, Peippo, M, Sipponen, M, Hartikainen, P, Ollokainen, M, Åman, J, Ignatius, J, Kärppä, M, Mustonen, A, Kajula, O, Jääskalainen, O, Moilanen, J, Santala, M, Eklund, P, Hiivola, H, Hyppönen, H

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