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Items where Author is "Bauer, Péter"

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Number of items: 7.

Tezenas du Montcel, Sophie and Durr, Alexandra and Rakowicz, Maria and Nanetti, Lorenzo and Charles, Perrine and Sulek, Anna and Mariotti, Caterina and Rola, Rafal and Schols, Ludger and Bauer, Péter and Dufaure-Garé, Isabelle and Jacobi, Heike and Forlani, Sylvie and Schmitz-Hübsch, Tanja and Filla, Alessandro and Timmann, Dagmar and van de Warrenburg, Bart P. and Marelli, Cecilia and Kang, Jun-Suk and Giunti, Paola and Cook, Arron and Balikó, László and Melegh, Béla and Boesch, Sylvia and Szymanski, Sandra and Berciano, José and Infante, Jon and Buerk, Katrin and Masciullo, Marcella and Fabio Di, Roberto and Depondt, Chantal and Ratka, Susanne and Stevanin, Giovanni and Klockgether, Thomas and Brice, Alexis and Golmard, Jean-Louis (2014) Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6. Journal of Medical Genetics, 51 (7). pp. 479-486. ISSN 0022-2593 (print), 1468-6244 (online)

Jacobi, Heike and Reetz, Kathrin and Tezenas du Montcel, Sophie and Bauer, Péter and Mariotti, Caterina and Nanetti, Lorenzo and Rakowicz, Maria and Sulek, Anna and Durr, Alexandra and Charles, Perrine and Filla, Alessandro and Antenora, Antonella and Schols, Ludger and Schicks, Julia and Infante, Jon and Kang, Jun-Suk and Timmann, Dagmar and Di Fabio, Roberto and Masciullo, Marcella and Balikó, László and Melegh, Béla and Boesch, Sylvia and Bürk, Katrin and Peltz, Annkathrin and Schulz B, Jörg and Dufaure-Garé, Isabelle and Klockgether, Thomas (2013) Biological and clinical characteristics of individuals at risk for spinocereellar ataxia types 1,2,3, and 6 in the longitudinal RISCA study: analysis of baseline data. Lancet Neurology, 12 (7). pp. 650-658. ISSN 1474-4422

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)

Bokor, József and Bauer, Péter and Bécsi, Tamás and Gáspár, Péter and Kulcsár, Balázs and Péni, Tamás and Péter, Tamás and Rödönyi, Gábor and Szabó, Zoltán and Varga, István (2010) Lineáris és paraméter függő lineáris kapcsoló üzemmódú rendszerek irányítása = Control of linear and parameter-varying switching mode systems. Project Report. OTKA.

Soumelidis, Alexandros and Gáspár, Péter and Bauer, Péter and Lantos, Béla and Prohászka, Zoltán (2007) Design of an embedded microcomputer based mini quadrotor UAV. In: European Control Conference. IEEE, Kos, pp. 2236-2241. ISBN 978-960-89028-5-5

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)

This list was generated on Sat Mar 28 06:17:17 2015 CET.