Search Results - Zygmunt Jamrozik

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  1. 1
    Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia

    Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia by GDJ Watts, Dana Thomasová, SK Ramdeen, Erin Fulchiero, SG Mehta, DA Drachman, C. Weihl, Zygmunt Jamrozik, Hubert Kwieciński, Anna Kamińska, VE Kimonis

    Published 2007
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    Artigo
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  2. 2
    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 by 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

    Published 2013
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    Artigo
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  3. 3
    Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options

    Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options by Albert C. Ludolph, Jan Kassubek, G. Bernhard Landwehrmeyer, E. Mandelkow, Eva‐Maria Mandelkow, David J. Burn, D Caparros-Lefèbvre, Kirk A. Frey, Justo Garcı́a de Yébenes, Thomas Gasser, Peter Heutink, Günter U. Höglinger, Zygmunt Jamrozik, K. A. Jellinger, A.D. Kazantsev, Hans Kretzschmar, Anthony E. Lang, Irene Litvan, José J. Lucas, Patrick L. McGeer, Stacey Melquist, Wolfgang H. Oertel, Markus Otto, Dominic Paviour, T. Reum, Agnès Saint-Raymond, John C. Steele, Markus Tolnay, Hayrettin Tumani, John C. van Swieten, M. T. Vanier, Jean‐Paul Vonsattel, Steven L. Wagner, Zbigniew K. Wszołek

    Published 2009
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    Revisão
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  4. 4
    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 by 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

    Published 2012
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