Výsledky vyhledávání - Grzegorz Opala

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  1. 1
    Early-onset Parkinson's disease due to PINK1 p.Q456X mutation – Clinical and functional study

    Early-onset Parkinson's disease due to PINK1 p.Q456X mutation – Clinical and functional study Autor Joanna Siuda, Barbara Jasińska‐Myga, Magdalena Boczarska‐Jedynak, Grzegorz Opala, Fabienne C. Fiesel, Elisabeth L. Moussaud-Lamodière, Leslie A. Scarffe, Valina L. Dawson, Owen A. Ross, Wolfdieter Springer, Ted M. Dawson, Zbigniew K. Wszołek

    Vydáno 2014
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  2. 2
    Genetic variation of Omi/HtrA2 and Parkinson's disease

    Genetic variation of Omi/HtrA2 and Parkinson's disease Autor Owen A. Ross, Alexandra I. Soto, Carles Vilariño‐Güell, Michael G. Heckman, Nancy N. Diehl, Mary Hulihan, Jan Aasly, Sigrid Botne Sando, J. Mark Gibson, Timothy Lynch, Anna Krygowska‐Wajs, Grzegorz Opala, Maria Barcikowska, K Czyźewski, Ryan J. Uitti, Zbigniew K. Wszołek, Matthew J. Farrer

    Vydáno 2008
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  3. 3
    Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease

    Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease Autor Dorota Hoffman‐Zacharska, Dariusz Koziorowski, Owen A. Ross, Michał Milewski, Jarosław Poznański, Marta Jurek, Zbigniew K. Wszołek, Alexandra I. Soto‐Ortolaza, Jarosław Sławek, Piotr Janik, Zygmunt Jamrozik, Anna Potulska‐Chromik, Barbara Jasińska‐Myga, Grzegorz Opala, Anna Krygowska‐Wajs, K Czyźewski, Dennis W. Dickson, Jerzy Bal, Andrzej Friedman

    Vydáno 2013
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  4. 4
    Heterozygous PINK1 p.G411S increases risk of Parkinson’s disease via a dominant-negative mechanism

    Heterozygous PINK1 p.G411S increases risk of Parkinson’s disease via a dominant-negative mechanism Autor Andreas Puschmann, Fabienne C. Fiesel, Thomas R. Caulfield, Roman Hudec, Maya Ando, Dominika Truban, Xu Hou, Kotaro Ogaki, Michael G. Heckman, Elle D. James, Maria Swanberg, Itzia Jiménez-Ferrer, Oskar Hansson, Grzegorz Opala, Joanna Siuda, Magdalena Boczarska‐Jedynak, Andrzej Friedman, Dariusz Koziorowski, Jan Aasly, Timothy Lynch, George D. Mellick, Megha Mohan, Peter A. Silburn, Yanosh Sanotsky, Carles Vilariño‐Güell, Matthew J. Farrer, Li Chen, Valina L. Dawson, Ted M. Dawson, Zbigniew K. Wszołek, Owen A. Ross, Wolfdieter Springer

    Vydáno 2016
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  5. 5
    Mitochondrial targeting sequence variants of the <i>CHCHD2</i> gene are a risk for Lewy body disorders

    Mitochondrial targeting sequence variants of the <i>CHCHD2</i> gene are a risk for Lewy body disorders Autor Kotaro Ogaki, Shunsuke Koga, Michael G. Heckman, Fabienne C. Fiesel, Maya Ando, Catherine Labbé, Oswaldo Lorenzo‐Betancor, Elisabeth L. Moussaud-Lamodière, Alexandra I. Soto‐Ortolaza, Ronald L. Walton, Audrey Strongosky, Ryan J. Uitti, Allan McCarthy, Timothy Lynch, Joanna Siuda, Grzegorz Opala, Monika Rudzińska, Anna Krygowska‐Wajs, Maria Barcikowska, K Czyźewski, Andreas Puschmann, Kenya Nishioka, Manabu Funayama, Nobutaka Hattori, Joseph E. Parisi, Ronald C. Petersen, Caroline Graff, Bradley F. Boeve, Wolfdieter Springer, Zbigniew K. Wszołek, Dennis W. Dickson, Owen A. Ross

    Vydáno 2015
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  6. 6
    A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease

    A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease Autor Rejko Krüger, Manu Sharma, Olaf Rieß, Thomas Gasser, Christine Van Broeckhoven, Jessie Theuns, Jan Aasly, Grazia Annesi, Anna Rita Bentivoglio, Alexis Brice, Ana Djarmati, Alexis Elbaz, Matthew J. Farrer, Carlo Ferrarese, J. Mark Gibson, Georgios M. Hadjigeorgiou, Nobutaka Hattori, John P. A. Ioannidis, Barbara Jasińska‐Myga, Christine Klein, Jean‐Charles Lambert, Suzanne Lesage, Juei-Jueng Lin, Timothy Lynch, George D. Mellick, Francesa de Nigris, Grzegorz Opala, Alessandro Prigione, Aldo Quattrone, Owen A. Ross, Wataru Satake, Peter A. Silburn, Eng King Tan, Tatsushi Toda, Hiroyuki Tomiyama, Karin Wirdefeldt, Zbigniew K. Wszołek, Georgia Xiromerisiou, Demetrius M. Maraganore

    Vydáno 2009
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  7. 7
    TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson’s disease

    TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson’s disease Autor Sruti Rayaprolu, Bianca Mullen, Matt Baker, Timothy Lynch, Elizabeth Finger, William W. Seeley, Kimmo J. Hatanpaa, Catherine Lomen‐Hoerth, Andrew Kertesz, Eileen H. Bigio, Carol F. Lippa, Keith A. Josephs, David S. Knopman, Charles L. White, Richard J. Caselli, Ian R. Mackenzie, Bruce L. Miller, Magdalena Boczarska‐Jedynak, Grzegorz Opala, Anna Krygowska‐Wajs, Maria Barcikowska, Steven G. Younkin, Ronald Petersen, Nilüfer Ertekin‐Taner, Ryan J. Uitti, James F. Meschia, Khrista Boylan, Bradley F. Boeve, Neill R. Graff‐Radford, Zbigniew K. Wszołek, Dennis W. Dickson, Rosa Rademakers, Owen A. Ross

    Vydáno 2013
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  8. 8
    Independent and joint effects of the <i>MAPT</i> and <i>SNCA</i> genes in Parkinson disease

    Independent and joint effects of the <i>MAPT</i> and <i>SNCA</i> genes in Parkinson disease Autor Alexis Elbaz, Owen A. Ross, John P. A. Ioannidis, Alexandra I. Soto‐Ortolaza, Frédéric Moisan, Jan Aasly, Grazia Annesi, Maria Bozi, Laura Brighina, Marie‐Christine Chartier‐Harlin, A. Destée, Carlo Ferrarese, Alessandro Ferraris, Jonathan Gibson, Suzana Gispert, Georgios M. Hadjigeorgiou, Barbara Jasińska‐Myga, Christine Klein, Rejko Krüger, Jean‐Charles Lambert, Katja Lohmann, Simone van de Loo, Marie‐Anne Loriot, Timothy Lynch, George D. Mellick, Eugénie Mutez, Christer Nilsson, Grzegorz Opala, Andreas Puschmann, Aldo Quattrone, Manu Sharma, Peter A. Silburn, Leonidas Stefanis, Ryan J. Uitti, Enza Maria Valente, Carles Vilariño‐Güell, Karin Wirdefeldt, Zbigniew K. Wszołek, Georgia Xiromerisiou, Demetrius M. Maraganore, Matthew J. Farrer

    Vydáno 2010
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  9. 9
    Pharmacological Rescue of Mitochondrial Deficits in iPSC-Derived Neural Cells from Patients with Familial Parkinson’s Disease

    Pharmacological Rescue of Mitochondrial Deficits in iPSC-Derived Neural Cells from Patients with Familial Parkinson’s Disease Autor Oliver Cooper, Hyemyung Seo, Shaida A. Andrabi, Cristina Guardia‐Laguarta, John J. Graziotto, Maria Sundberg, Jesse R. McLean, Luis Carrillo‐Reid, Zhong Xie, Teresia Osborn, Gunnar Hargus, Michela Deleidi, Tristan Lawson, Helle Bogetofte, Eduardo Pérez-Torres, Lorraine N. Clark, Carol Moskowitz, Joseph R. Mazzulli, Li Chen, Laura A. Volpicelli‐Daley, Norma B. Romero, Houbo Jiang, Ryan J. Uitti, Zhigao Huang, Grzegorz Opala, Leslie A. Scarffe, Valina L. Dawson, Christine Klein, Jian Feng, Owen A. Ross, John Q. Trojanowski, Virginia M.‐Y. Lee, Karen Marder, D. James Surmeier, Zbigniew K. Wszołek, Serge Przedborski, Dimitri Krainc, Ted M. Dawson, Ole Isacson

    Vydáno 2012
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  10. 10
    Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research

    Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research Autor Selina Wray, Matthew W. Self, Patrick A. Lewis, Jan‐Willem Taanman, Natalie S. Ryan, Colin Mahoney, Yuying Liang, Michael J. Devine, Una‐Marie Sheerin, Henry Houlden, Huw R. Morris, Daniel G. Healy, J.F. Martí-Massó, Elisavet Preza, Suzanne Barker, Margaret Sutherland, Roderick A. Corriveau, Michael R. D’Andrea, Anthony H.V. Schapira, Ryan J. Uitti, Mark Guttman, Grzegorz Opala, Barbara Jasińska‐Myga, Andreas Puschmann, Christer Nilsson, Alberto J. Espay, Jarosław Sławek, Ludwig Gutmann, Bradley F. Boeve, Khrista Boylan, A. Jon Stoessl, Owen A. Ross, Nicholas J. Maragakis, Jay Van Gerpen, Melissa Gerstenhaber, Katrina Gwinn, Ted M. Dawson, Ole Isacson, Karen Marder, Lorraine N. Clark, Serge Przedborski, Steven Finkbeiner, Jeffrey D. Rothstein, Zbigniew K. Wszołek, Martin N. Rossor, John Hardy

    Vydáno 2012
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  11. 11
    Global investigation and meta-analysis of the <i>C9orf72</i> (G <sub>4</sub> C <sub>2</sub> ) <sub>n</sub> repeat in Parkinson disease

    Global investigation and meta-analysis of the <i>C9orf72</i> (G <sub>4</sub> C <sub>2</sub> ) <sub>n</sub> repeat in Parkinson disease Autor Jessie Theuns, Aline Verstraeten, Kristel Sleegers, Eline Wauters, Ilse Gijselinck, Stefanie Smolders, David Crosiers, Ellen Corsmit, Ellen Elinck, Manu Sharma, Rejko Krüger, Suzanne Lesage, Alexis Brice, Sun Ju Chung, Mi‐Jung Kim, Young Jin Kim, Owen A. Ross, Zbigniew K. Wszołek, Ekaterina Rogaeva, Zhengrui Xi, Anthony E. Lang, Christine Klein, Anne Weißbach, George D. Mellick, Peter A. Silburn, Georgios M. Hadjigeorgiou, Efthimios Dardiotis, Nobutaka Hattori, Kotaro Ogaki, Eng‐King Tan, Yi Zhao, Jan Aasly, Enza Maria Valente, Simona Petrucci, Grazia Annesi, Aldo Quattrone, Carlo Ferrarese, Laura Brighina, Angela Deutschländer, Andreas Puschmann, Christer Nilsson, Gaëtan Garraux, Mark S. LeDoux, Ronald F. Pfeiffer, Magdalena Boczarska‐Jedynak, Grzegorz Opala, Demetrius M. Maraganore, Sebastiaan Engelborghs, Peter Paul De Deyn, Patrick Cras, Marc Cruts, Christine Van Broeckhoven

    Vydáno 2014
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  12. 12
    Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease

    Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease Autor Marie‐Christine Chartier‐Harlin, Justus C. Dächsel, Carles Vilariño‐Güell, Sarah Lincoln, Frédéric Leprêtre, Mary Hulihan, Jennifer M. Kachergus, Austen J. Milnerwood, Lucı́a Tapia, Mee-Sook Song, Émilie Le Rhun, Eugénie Mutez, Lydie Larvor, Aurélie Duflot, Christel Vanbesien-Mailliot, Alexandre Kreisler, Owen A. Ross, Kenya Nishioka, Alexandra I. Soto‐Ortolaza, Stephanie A. Cobb, Heather L. Melrose, Bahareh Behrouz, Brett H. Keeling, Justin A. Bacon, Emna Hentati, Lindsey N. Williams, Akiko Yanagiya, Nahum Sonenberg, Paul J. Lockhart, Abba C. Zubair, Ryan J. Uitti, Jan Aasly, Anna Krygowska‐Wajs, Grzegorz Opala, Zbigniew K. Wszołek, Roberta Frigerio, Demetrius M. Maraganore, David Gosal, Tim Lynch, Michael Hutchinson, Anna Rita Bentivoglio, Enza Maria Valente, William C. Nichols, Nathan Pankratz, Tatiana Foroud, Rachel A. Gibson, Fayçal Hentati, Dennis W. Dickson, A. Destée, Matthew J. Farrer

    Vydáno 2011
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  13. 13
    A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

    A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants Autor Manu Sharma, John P. A. Ioannidis, Jan Aasly, Grazia Annesi, Alexis Brice, Lars Bertram, Maria Bozi, Maria Barcikowska, David Crosiers, Carl E Clarke, Maurizio Facheris, Matthew J. Farrer, Gaëtan Garraux, Suzana Gispert, Georg Auburger, Carles Vilariño‐Güell, Georgios M. Hadjigeorgiou, Andrew A. Hicks, Nobutaka Hattori, Beom S. Jeon, Zygmunt Jamrozik, Anna Krygowska‐Wajs, Suzanne Lesage, Christina M. Lill, Juei‐Jueng Lin, Timothy Lynch, Peter Lichtner, Anthony E. Lang, Cécile Libioulle, Miho Murata, Vincent Mok, Barbara Jasińska‐Myga, George D. Mellick, Karen Morrison, Thomas Meitnger, Alexander Zimprich, Grzegorz Opala, Peter P. Pramstaller, Irene Pichler, Sung Sup Park, Aldo Quattrone, Ekaterina Rogaeva, Owen A. Ross, Leonidas Stefanis, Joanne Stockton, Wataru Satake, Peter A. Silburn, Tim M. Strom, Jessie Theuns, Eng King Tan, Tatsushi Toda, Hiroyuki Tomiyama, Ryan J. Uitti, Christine Van Broeckhoven, Karin Wirdefeldt, Zbigniew K. Wszołek, Georgia Xiromerisiou, Harumi Yomono, Kuo-Chu Yueh, Yi Zhao, Thomas Gasser, Demetrius M. Maraganore, Rejko Krüger

    Vydáno 2012
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  14. 14
    Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study

    Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study Autor Owen A. Ross, Alexandra I. Soto‐Ortolaza, Michael G. Heckman, Jan Aasly, Nadine Abahuni, Grazia Annesi, Justin A. Bacon, Soraya Bardien, Maria Bozi, Alexis Brice, Laura Brighina, Christine Van Broeckhoven, Jonathan Carr, Marie‐Christine Chartier‐Harlin, Efthimios Dardiotis, Dennis W. Dickson, Nancy N. Diehl, Alexis Elbaz, Carlo Ferrarese, Alessandro Ferraris, Brian Fiske, J. Mark Gibson, Rachel A. Gibson, Georgios M. Hadjigeorgiou, Nobutaka Hattori, John P. A. Ioannidis, Barbara Jasińska‐Myga, Beom S. Jeon, Yun Joong Kim, Christine Klein, Rejko Krüger, Elli Kyratzi, Suzanne Lesage, Chin‐Hsien Lin, Timothy Lynch, Demetrius M. Maraganore, George D. Mellick, Eugénie Mutez, Christer Nilsson, Grzegorz Opala, Sung Sup Park, Andreas Puschmann, Aldo Quattrone, Manu Sharma, Peter A. Silburn, Young H. Sohn, Leonidas Stefanis, Vera Tadić, Jessie Theuns, Hiroyuki Tomiyama, Ryan J. Uitti, Enza Maria Valente, Simone van de Loo, Demetrios K. Vassilatis, Carles Vilariño‐Güell, Linda R. White, Karin Wirdefeldt, Zbigniew K. Wszołek, Ruey‐Meei Wu, Matthew J. Farrer

    Vydáno 2011
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  15. 15
    Large-scale replication and heterogeneity in Parkinson disease genetic loci

    Large-scale replication and heterogeneity in Parkinson disease genetic loci Autor Manu Sharma, John P. A. Ioannidis, Jan Aasly, Grazia Annesi, Alexis Brice, Christine Van Broeckhoven, Lars Bertram, Maria Bozi, David Crosiers, Carl E Clarke, Maurizio Facheris, Matthew J. Farrer, Gaëtan Garraux, Suzana Gispert, Georg Auburger, Carles Vilariño‐Güell, Georgios M. Hadjigeorgiou, Andrew A. Hicks, Nobutaka Hattori, Beom S. Jeon, Suzanne Lesage, Christina M. Lill, Juei-Jueng Lin, Timothy Lynch, Peter Lichtner, Anthony E. Lang, Vincent Mok, Barbara Jasińska‐Myga, George D. Mellick, Karen Morrison, Grzegorz Opala, Peter P. Pramstaller, Irene Pichler, Sung Sup Park, Aldo Quattrone, Ekaterina Rogaeva, Owen A. Ross, Leonidas Stefanis, Joanne Stockton, Wataru Satake, Peter A. Silburn, Jessie Theuns, Eng-King Tan, Tatsushi Toda, Hiroyuki Tomiyama, Ryan J. Uitti, Karin Wirdefeldt, Zbigniew K. Wszołek, Georgia Xiromerisiou, Kuo-Chu Yueh, Yi Zhao, Thomas Gasser, Demetrius M. Maraganore, Rejko Krüger, R.S Boyle, A Sellbach, John D. O’Sullivan, Greg T. Sutherland, G. Siebert, N. Dissanayaka, Christine Van Broeckhoven, Jessie Theuns, David Crosiers, Barbara Pickut, Sebastiaan Engelborghs, Bram Meeus, Peter Paul De Deyn, Patrick Cras, Ekaterina Rogaeva, Anthony E. Lang, Y. Agid, Mathieu Anheim, A-M Bonnet, Michael Borg, Alexis Brice, E. Broussolle, Jean‐Christophe Corvol, Philippe Damier, A. Destée, Alexandra Dürr, F. Durif, Suzanne Lesage, Ebba Lohmann, Pierre Pollak, Olivier Rascol, François Tison, Christine Tranchant, François Viallet, Marie Vidailhet, Christophe Tzourio, Philippe Amouyel, Marie‐Anne Loriot, Eugénie Mutez, Aurélie Duflot, Jean-Philippe Legendre, Nawal Waucquier, Thomas Gasser, Olaf Rieß, Daniela Berg, Claudia Schulte

    Vydáno 2012
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