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Items where Author is "Ribai, Pascale"

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Number of items: 5.

Article

Jacobi, Heike and Hauser, Till-Karsten and Giunti, Paola and Globas, Christoph and Bauer, Péter and Schmitz-Hübsch, Tanja and Balikó, László and Filla, Alessandro and Mariotti, Caterina and Rakowicz, Maria and Charles, Perrine and Ribai, Pascale and Szymanski, Sandra and Infante, Jon and van de Warrenburg, Bart P.C. and Durr, Alexandra and Timmann, Dagmar and Boesch, Sylvia and Fancellu, Roberto and Rola, Rafal and Depondt, Chantal and Schols, Ludger and Zdzienicka, Elzbieta and Kang, Jun-Suk and Ratzka, Susanne and Kremer, Berry and Stephenson, Dennis A. and Melegh, Béla and Pandolfo, Massimo and du Montcel, Sophie Tezenas and Borkert, Johannes and Schulz B., Jörg and Klockgether, Thomas (2012) Spinocerebellar Ataxia Types 1, 2, 3 and 6: the Clinical Spectrum of Ataxia and Morphometric Brainstem and cerebellar Findings. Cerebellum, 11 (1). pp. 155-166. ISSN 1473-4222 (Print) 1473-4230 (Online)

Schmitz-Hübsch, Tanja and Coudert, Mathieu and du Montcel, Sophie Tezenas and Giunti, Paola and Labrum, Robyn and Durr, Alexandra and Ribai, Pascale and Charles, Perrine and Linnemann, Christoph and Schols, Ludger and Rakowicz, Maria and Rola, Rafal and Zdzienicka, Elzbieta and Fancellu, Roberto and Mariotti, Caterina and Balikó, László and Melegh, Béla and Filla, Alessandro and Salvatore, Elena and van de Warrenburg, Bart P. C. and Szymanski, Sandra and Infante, Jon and Timmann, Dagmar and Boesch, Sylvia and Depondt, Chantal and Kang, Jun-Suk and Schulz B., Jörg and Klopstock, Thomas and Lossnitzer, Nicole and Löwe, Bernd and Frick, Caroline and Rottlander, Daniela and Schlaepfer, E. Thomas and Klockgether, Thomas (2011) Depression comorbidity in spinocerebellar ataxia. MOVEMENT DISORDERS, 25 (5). pp. 870-876. ISSN 0885-3185

Globas, Christoph and Tezenas du Montcel, Sophie and Balikó, László and Boesch, Sylvia and Depondt, Chantal and DiDonato, Stefano and Durr, Alexandra and Filla, Alessandro and Klockgether, Thomas and Mariotti, Caterina and Melegh, Béla and Rakowicz, Maria and Ribai, Pascale and Rola, Rafal and Schmitz-Hübsch, Tanja and Szymanski, Sandra and Timmann, Dagmar and van de Warrenburg, Bart P. and Bauer, Péter and Schols, Ludger (2008) Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6. MOVEMENT DISORDERS, 23 (15). pp. 2232-2238. ISSN 0885-3185

Metzger, Silke and Bauer, Péter and Tomiuk, Jürgen and Laccone, Franco and DiDonato, Stefano and Gellera, Cinzia and Mariotti, Caterina and Lange, Herwig W. and Weirich-Schwaiger, Helga and Wenning, Gregor K. and Seppi, Klaus and Melegh, Béla and Havasi, Viktória and Balikó, László and Wieczorek, Stefan and Zaremba, Jacek and Hoffman-Zacharska, Dorota and Sulek, Anna and Basak, Nazli A. and Soydan, Esra and Zidovska, Jana and Kebrdlova, Vera and Pandolfo, Massimo and Ribai, Pascale and Kadasi, Ludovit and Kvasnicova, Marta and Weber, Bernhardt H. F. and Kreuz, Friedmar and Dose, Matthias and Stuhrmann, Manfred and Riess, Olaf (2006) Genetic analysis of candidate genes modifying the age-atonset in Hungtinton's disease. Human Genetics, 20 (2). pp. 285-292. ISSN 0340-6717 (Print); 1432-1203 (Online)

Metzger, Silke and Bauer, Péter and Tomiuk, Jürgen and Laccone, Franco and DiDonato, Stefano and Gellera, Cinzia and Soliveri, Paola and Lange, Herwig W. and Weirich-Schwaiger, Helga and Wenning, Gregor K. and Melegh, Béla and Havasi, Viktória and Balikó, László and Wieczorek, Stefan and Arning, Larissa and Zaremba, Jacek and Sulek, Anna and Hoffman-Zacharska, Dorota and Basak, Nazli A. and Ersoy, Nagehan and Zidovska, Jana and Kebrdlova, Vera and Pandolfo, Massimo and Ribai, Pascale and Kadasi, Ludovit and Kvasnicova, Marta and Weber, Bernhardt H. F. and Kreuz, Friedmar and Dose, Matthias and Stuhrmann, Manfred and Riess, Olaf (2006) The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease. Neurogenetics, 7 (1). pp. 27-30. ISSN ISSN: 1364-6745 (Print) 1364-6753 (Online)

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