检索结果 - Alexandra I. Soto‐Ortolaza

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  1. 1
    Neuropathologically defined subtypes of Alzheimer’s disease differ significantly from neurofibrillary tangle-predominant dementia

    Neuropathologically defined subtypes of Alzheimer’s disease differ significantly from neurofibrillary tangle-predominant dementia 由 Nicholas J. Janocko, Kevin Brodersen, Alexandra I. Soto‐Ortolaza, Owen A. Ross, Amanda M. Liesinger, Ranjan Duara, Neill R. Graff‐Radford, Dennis W. Dickson, Melissa E. Murray

    出版 2012
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  2. 2
    TARDBP mutations in Parkinson's disease

    TARDBP mutations in Parkinson's disease 由 Sruti Rayaprolu, Shinsuke Fujioka, Sharleen Traynor, Alexandra I. Soto‐Ortolaza, Leonard Petrucelli, Dennis W. Dickson, Rosa Rademakers, Khrista Boylan, Neill R. Graff‐Radford, Ryan J. Uitti, Zbigniew K. Wszołek, Owen A. Ross

    出版 2012
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  3. 3
    <i>MAPT</i> H1 haplotype is a risk factor for essential tremor and multiple system atrophy

    <i>MAPT</i> H1 haplotype is a risk factor for essential tremor and multiple system atrophy 由 Carles Vilariño‐Güell, Alexandra I. Soto‐Ortolaza, Alex Rajput, Deborah C. Mash, Spyridon Papapetropoulos, Rajesh Pahwa, Kelly E. Lyons, Ryan J. Uitti, Zbigniew K. Wszołek, Dennis W. Dickson, Matthew J. Farrer, Owen A. Ross

    出版 2011
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  4. 4
    Association of the <i>MAPT</i> locus with Parkinson’s disease

    Association of the <i>MAPT</i> locus with Parkinson’s disease 由 Christian Wider, Carles Vilariño‐Güell, Barbara Jasińska‐Myga, Michael G. Heckman, Alexandra I. Soto‐Ortolaza, Stephanie A. Cobb, Jan Aasly, J. Mark Gibson, Timothy Lynch, Ryan J. Uitti, Zbigniew K. Wszołek, Matthew J. Farrer, Owen A. Ross

    出版 2009
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  5. 5
    Association of α-, β-, and γ-Synuclein With Diffuse Lewy Body Disease

    Association of α-, β-, and γ-Synuclein With Diffuse Lewy Body Disease 由 Kenya Nishioka, Christian Wider, Carles Vilariño‐Güell, Alexandra I. Soto‐Ortolaza, Sarah Lincoln, Jennifer M. Kachergus, Barbara Jasińska‐Myga, Owen A. Ross, Alex Rajput, Christopher A. Robinson, Tanis J. Ferman, Zbigniew K. Wszołek, Dennis W. Dickson, Matthew J. Farrer

    出版 2010
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  6. 6
    Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank

    Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank 由 Kevin F. Bieniek, Owen A. Ross, Kerry A. Cormier, Ronald L. Walton, Alexandra I. Soto‐Ortolaza, Amelia Johnston, Pamela Desaro, Khrista Boylan, Neill R. Graff‐Radford, Zbigniew K. Wszołek, Rosa Rademakers, Bradley F. Boeve, Ann C. McKee, Dennis W. Dickson

    出版 2015
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  7. 7
    <scp>S</scp>tudy of <i>LRRK2</i> variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration

    <scp>S</scp>tudy of <i>LRRK2</i> variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration 由 Mónica Sánchez-Contreras, Michael G. Heckman, Paweł Tacik, Nancy N. Diehl, Patricia H. Brown, Alexandra I. Soto‐Ortolaza, Elizabeth Christopher, Ronald L. Walton, Owen A. Ross, Lawrence I. Golbe, Neill R. Graff‐Radford, Zbigniew K. Wszołek, Dennis W. Dickson, Rosa Rademakers

    出版 2016
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  8. 8
    Identification of genetic modifiers of age-at-onset for familial Parkinson’s disease

    Identification of genetic modifiers of age-at-onset for familial Parkinson’s disease 由 Erin M. Hill‐Burns, Owen A. Ross, William T. Wissemann, Alexandra I. Soto‐Ortolaza, Sepideh Zareparsi, Joanna Siuda, Timothy Lynch, Zbigniew K. Wszołek, Peter A. Silburn, George D. Mellick, Beate Ritz, Clemens R. Scherzer, Cyrus P. Zabetian, Stewart A. Factor, Patrick Breheny, Haydeh Payami

    出版 2016
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  9. 9
    LINGO1 rs9652490 is associated with essential tremor and Parkinson disease

    LINGO1 rs9652490 is associated with essential tremor and Parkinson disease 由 Carles Vilariño‐Güell, Owen A. Ross, Christian Wider, Barbara Jasińska‐Myga, Stephanie A. Cobb, Alexandra I. Soto‐Ortolaza, Jennifer M. Kachergus, Brett H. Keeling, Justus C. Dächsel, Heather L. Melrose, Bahareh Behrouz, Zbigniew K. Wszołek, Ryan J. Uitti, Jan Aasly, Alex Rajput, Matthew J. Farrer

    出版 2009
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  10. 10
    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 由 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

    出版 2013
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  11. 11
    Analysis of COQ2gene in multiple system atrophy

    Analysis of COQ2gene in multiple system atrophy 由 Kotaro Ogaki, Shinsuke Fujioka, Michael G. Heckman, Sruti Rayaprolu, Alexandra I. Soto‐Ortolaza, Catherine Labbé, Ronald L. Walton, Oswaldo Lorenzo‐Betancor, Xue Wang, Yan W. Asmann, Rosa Rademakers, Neill R. Graff‐Radford, Ryan J. Uitti, William P. Cheshire, Zbigniew K. Wszołek, Dennis W. Dickson, Owen A. Ross

    出版 2014
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  12. 12
    Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease

    Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease 由 Jan Aasly, Carles Vilariño‐Güell, Justus C. Dächsel, Philip J. Webber, Andrew B. West, Kristoffer Haugarvoll, Krisztina K. Johansen, Mathias Toft, John G. Nutt, Haydeh Payami, Jennifer M. Kachergus, Sarah Lincoln, Amela Felic, Christian Wider, Alexandra I. Soto‐Ortolaza, Stephanie A. Cobb, Linda R. White, Owen A. Ross, Matthew J. Farrer

    出版 2010
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  13. 13
    LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease

    LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease 由 Carles Vilariño‐Güell, Christian Wider, Owen A. Ross, Barbara Jasińska‐Myga, Jennifer M. Kachergus, Stephanie A. Cobb, Alexandra I. Soto‐Ortolaza, Bahareh Behrouz, Michael G. Heckman, Nancy N. Diehl, Claudia Testa, Zbigniew K. Wszołek, Ryan J. Uitti, Joseph Jankovic, Elan D. Louis, Lorraine N. Clark, Alex Rajput, Matthew J. Farrer

    出版 2010
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  14. 14
    <i>LRRK2</i> exonic variants and risk of multiple system atrophy

    <i>LRRK2</i> exonic variants and risk of multiple system atrophy 由 Michael G. Heckman, Lucía Schottlaender, Alexandra I. Soto‐Ortolaza, Nancy N. Diehl, Sruti Rayaprolu, Kotaro Ogaki, Shinsuke Fujioka, Melissa E. Murray, William P. Cheshire, Ryan J. Uitti, Zbigniew K. Wszołek, Matthew J. Farrer, Anna Sailer, Andrew Singleton, Patrick F. Chinnery, Michael J. Keogh, Steve Gentleman, Janice L. Holton, Kiely Aoife, David M. A. Mann, Safa Al‐Sarraj, Claire Troakes, Dennis W. Dickson, Henry Houlden, Owen A. Ross

    出版 2014
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  15. 15
    Characterization of <i>DCTN1</i> genetic variability in neurodegeneration

    Characterization of <i>DCTN1</i> genetic variability in neurodegeneration 由 Carles Vilariño‐Güell, Christian Wider, Alexandra I. Soto‐Ortolaza, Stephanie A. Cobb, Jennifer M. Kachergus, Brett H. Keeling, Justus C. Dächsel, Mary Hulihan, Dennis W. Dickson, Zbigniew K. Wszołek, Ryan J. Uitti, Neill R. Graff‐Radford, B. F. Boeve, K. Josephs, Bruce L. Miller, Khrista Boylan, Katrina Gwinn, Charles H. Adler, Jan Aasly, Fayçal Hentati, A. Destée, Anna Krygowska‐Wajs, Marie‐Christine Chartier‐Harlin, Owen A. Ross, Rosa Rademakers, Matthew J. Farrer

    出版 2009
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  16. 16
    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 由 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

    出版 2015
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  17. 17
    LRRK2 variation and dementia with Lewy bodies

    LRRK2 variation and dementia with Lewy bodies 由 Michael G. Heckman, Alexandra I. Soto‐Ortolaza, Mónica Sánchez-Contreras, Melissa E. Murray, Otto Pedraza, Nancy N. Diehl, Ronald L. Walton, Catherine Labbé, Oswaldo Lorenzo‐Betancor, Ryan J. Uitti, Jay Van Gerpen, Nilüfer Ertekin‐Taner, Glenn E. Smith, Kejal Kantarci, Rodolfo Savica, David T. Jones, Jonathan Graff‐Radford, David S. Knopman, Val J. Lowe, Clifford R. Jack, Ronald C. Petersen, Joseph E. Parisi, Rosa Rademakers, Zbigniew K. Wszołek, Neill R. Graff‐Radford, Tanis J. Ferman, Dennis W. Dickson, Bradley F. Boeve, Owen A. Ross

    出版 2016
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  18. 18
    VPS35 Mutations in Parkinson Disease

    VPS35 Mutations in Parkinson Disease 由 Carles Vilariño‐Güell, Christian Wider, Owen A. Ross, Justus C. Dächsel, Jennifer M. Kachergus, Sarah Lincoln, Alexandra I. Soto‐Ortolaza, Stephanie A. Cobb, Greggory J. Wilhoite, Justin A. Bacon, Bahareh Behrouz, Heather L. Melrose, Emna Hentati, Andreas Puschmann, Daniel M. Evans, Elizabeth Conibear, Wyeth W. Wasserman, Jan Aasly, Pierre R. Burkhard, Ruth Djaldetti, Joseph Ghika, Fayçal Hentati, Anna Krygowska‐Wajs, Tim Lynch, Eldad Melamed, Alex Rajput, Ali H. Rajput, Alessandra Solida, Ruey‐Meei Wu, Ryan J. Uitti, Zbigniew K. Wszołek, François Vingerhoets, Matthew J. Farrer

    出版 2011
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  19. 19
    Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype

    Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype 由 Nicola J. Rutherford, Michael G. Heckman, Mariely DeJesus‐Hernandez, Matt Baker, Alexandra I. Soto‐Ortolaza, Sruti Rayaprolu, Heather Stewart, Elizabeth Finger, Kathryn Volkening, William W. Seeley, Kimmo J. Hatanpaa, Catherine Lomen‐Hoerth, Andrew Kertesz, Eileen H. Bigio, Carol F. Lippa, David S. Knopman, Hans A. Kretzschmar, Manuela Neumann, Richard J. Caselli, Charles L. White, Ian R. Mackenzie, Ronald Petersen, Michael J. Strong, Bruce L. Miller, Bradley F. Boeve, Ryan J. Uitti, Khrista Boylan, Zbigniew K. Wszołek, Neill R. Graff‐Radford, Dennis W. Dickson, Owen A. Ross, Rosa Rademakers

    出版 2012
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  20. 20
    Ataxin-2 repeat-length variation and neurodegeneration

    Ataxin-2 repeat-length variation and neurodegeneration 由 Owen A. Ross, Nicola J. Rutherford, Matthew Baker, Alexandra I. Soto‐Ortolaza, Minerva M. Carrasquillo, M. DeJesus-Hernandez, Joy Adamson, M. Li, Kathryn Volkening, Elizabeth Finger, William W. Seeley, Kimmo J. Hatanpaa, Catherine Lomen‐Hoerth, Andrew Kertesz, Eileen H. Bigio, Carol F. Lippa, Bryan K. Woodruff, David S. Knopman, Charles L. White, Jay A. van Gerpen, James F. Meschia, Ian R. Mackenzie, Khrista Boylan, Bradley F. Boeve, Bruce L. Miller, Michael J. Strong, Ryan J. Uitti, Steven G. Younkin, N. R. Graff-Radford, Ronald Petersen, Zbigniew K. Wszołek, Dennis W. Dickson, Rosa Rademakers

    出版 2011
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