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Items where Author is "Balikó, László"

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Number of items: 19.

Article

Hadzsiev, Kinga and Szőts, Mónika and Fekete, Anett and Balikó, László and Boycott, Kim and Nagy, Ferenc and Melegh, Béla (2017) Neuroacanthocytosis diagnózisa új generációs exom-szekvenálással | Neuroacanthocytosis diagnosis with new generation whole exome sequencing. Orvosi Hetilap, 158 (42). pp. 1681-1684. ISSN 0030-6002

Hadzsiev, Kinga and Balikó, László and Komlósi, Katalin and Lőcsei-Fekete, Anett and Csábi, Györgyi and Bene, Judit and Kisfali, Péter and Melegh, Béla (2015) Genetic testing of hereditary spastic paraplegia. Orvosi Hetilap, 156 (3). pp. 113-117. ISSN 0030-6002

Hadzsiev, Kinga and Balikó, László and Komlósi, Katalin and Lőcsei-Fekete, Anett and Csábi, Györgyi and Bene, Judit and Kisfali, Péter and Melegh, Béla (2015) Herediter spasticus paraplegia genetikai vizsgálata. Orvosi Hetilap, 156 (3). pp. 113-117. ISSN 0030-6002 (print), 1788-6120 (online)

Hadzsiev, Kinga and Balikó, László and Komlósi, Katalin and Lőcsei-Fekete, Anett and Csábi, Györgyi and Bene, Judit and Kisfali, Péter and Melegh, Béla (2015) Herediter spasticus paraplegia genetikai vizsgálata. Orvosi Hetilap, 156 (3). pp. 113-117. ISSN 0030-6002

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)

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

Maász, Anita and Szolnoki, Zoltán and Balikó, László and Melegh, Béla (2011) Ischaemiás stroke genetikai háttere: Hol tartunk most? Orvosi Hetilap, 152 (12). pp. 455-463. ISSN 0030-6002 (print), 1788-6120 (online)

Maász, Anita and Szolnoki, Zoltán and Balikó, László and Melegh, Béla (2011) Ischaemiás stroke genetikai háttere: Hol tartunk most? = Genetics of ischemic stroke: where are we now? Orvosi Hetilap, 152 (12). pp. 455-463. ISSN 0030-6002

Fonteyn M.R., Ella and Schmitz-Hübsch, Tanja and Verstappen C., Carla and Balikó, László and Bloem R., Bastian and Boesch, Sylvia and Bunn, Lisa and Charles, Perrine and Durr, Alexandra and Filla, Alessandro and Giunti, Paola and Globas, Christoph and Klockgether, Thomas and Melegh, Béla and Pandolfo, Massimo and Rosa De, Anna and Schols, Ludger and Timmann, Dagmar and Munneke, Marten and Kremer P.H., Berry and van de Warrenburg, Bart P.C. (2010) Falls in Spinocerebellar Ataxias: Results of the EuroSCA Fall Study. Cerebellum, 9 (2). pp. 232-239. ISSN 1473-4222 (Print) 1473-4230 (Online)

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

Schmitz-Hübsch, Tanja and Giunti, Paola and Stephenson, D. A. and Globas, Christoph and Balikó, László and Sacca, F. and Mariotti, C. and Rakowicz, M. and Szymanski, Sandra and Infante, Jon and van de Warrenburg, Bart P. and Timmann, D. and Fancellu, R. and Rola, R. and Depondt, Chantal and Schöls, L. and Zdzienicka, E. and Kang, J.-S. and Döhlinger, S. and Kremer, B. and Melegh, B. and Filla, A. and Klockgether, T. (2008) SCA Functional Index. A useful compound performance measure for spinocerebellar ataxia. Neurology, 71 (7). pp. 486-492. ISSN 1526-632X

Sáfrány, Enikő and Balikó, László and Guseo, András and Faragó, Bernadett and Melegh, Béla (2007) Autoszomális domináns öröklődésű cereballaris ataxiák. Orvosi Hetilap, 148 (45). pp. 2125-2132. ISSN 0030-6002 (print), 1788-6120 (online)

Sáfrány, Enikő and Balikó, László and Guseo, András and Faragó, Bernadett and Melegh, Béla (2007) Autoszomális domináns öröklődésű cerebellaris ataxiák = The autosomal dominant cerebellar ataxias are hereditary neurodegenerative diseases. Orvosi Hetilap, 148 (45). pp. 2125-2132. ISSN 0030-6002 (print); 1788-6120 (online)

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)

Schmitz-Hübsch, Tanja and Tezenas du Montcel, Sophie and Balikó, László and Boesch, Sylvia and Bonato, Sara and Fancellu, Roberto and Giunti, Paola and Globas, Christoph and Kang, Jun-Suk and Kremer, Berry and Mariotti, Caterina and Melegh, Béla and Rakowicz, Maria and Rola, Rafal and Romano, Sylvie and Schöls, Lodger and Szymanski, Sandra and van de Warrenburg, Bart P. C. and Zdzienicka, Elzbieta and Durr, Alexandra and Klockgether, Thomas (2006) Reliability and Validity of the international cooperative ataxia rating scale: A study in 156 spinocerebellar ataxia patients. MOVEMENT DISORDERS, 21 (5). pp. 969-704. ISSN 0885-3185

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)

Balikó, László and Csala, Béla and Czopf, József (2004) Suicide in Hungarian Huntington's Disease Patients. Neuroepidemiology, 23 (5). pp. 258-260. ISSN ISSN: 0251-5350 (Print) e-ISSN: 1423-0208 (Online

This list was generated on Sat Mar 22 05:27:44 2025 CET.