Works matching AU Gurevich, Tanya


Results: 71
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    Intact working memory in non-manifesting LRRK2 carriers -- an fMRI study.

    Published in:
    European Journal of Neuroscience, 2016, v. 43, n. 1, p. 106, doi. 10.1111/ejn.13120
    By:
    • Thaler, Avner;
    • Helmich, Rick C.;
    • Or‐Borichev, Ayelet;
    • Nuenen, Bart F.L.;
    • Shapira‐Lichter, Irit;
    • Gurevich, Tanya;
    • Orr‐Urtreger, Avi;
    • Marder, Karen;
    • Bressman, Susan;
    • Bloem, Bastiaan R.;
    • Giladi, Nir;
    • Hendler, Talma;
    • Mirelman, Anat;
    • Munoz, Doug
    Publication type:
    Article
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    Tossing and Turning in Bed: Nocturnal Movements in Parkinson's Disease.

    Published in:
    2020
    By:
    • Mirelman, Anat;
    • Hillel, Inbar;
    • Rochester, Lynn;
    • Del Din, Silvia;
    • Bloem, Bastiaan R.;
    • Avanzino, Laura;
    • Nieuwboer, Alice;
    • Maidan, Inbal;
    • Herman, Talia;
    • Thaler, Avner;
    • Gurevich, Tanya;
    • Kestenbaum, Meir;
    • Orr‐Urtreger, Avi;
    • Brys, Mirek;
    • Cedarbaum, Jesse M.;
    • Giladi, Nir;
    • Hausdorff, Jeffrey M.;
    • Orr-Urtreger, Avi
    Publication type:
    journal article
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    Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriers.

    Published in:
    2018
    By:
    • Mirelman, Anat;
    • Saunders‐Pullman, Rachel;
    • Alcalay, Roy N.;
    • Shustak, Shiran;
    • Thaler, Avner;
    • Gurevich, Tanya;
    • Raymond, Deborah;
    • Mejia‐Santana, Helen;
    • Orbe Reilly, Martha;
    • Ozelius, Laurie;
    • Clark, Lorraine;
    • Gana‐Weisz, Mali;
    • Bar‐Shira, Anat;
    • Orr‐Utreger, Avi;
    • Bressman, Susan B.;
    • Marder, Karen;
    • Giladi, Nir;
    • the AJ LRRK2 Consortium;
    • Saunders-Pullman, Rachel;
    • Mejia-Santana, Helen
    Publication type:
    journal article
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    Arm swing as a potential new prodromal marker of Parkinson's disease.

    Published in:
    2016
    By:
    • Mirelman, Anat;
    • Bernad‐Elazari, Hagar;
    • Thaler, Avner;
    • Giladi‐Yacobi, Eytan;
    • Gurevich, Tanya;
    • Gana‐Weisz, Mali;
    • Saunders‐Pullman, Rachel;
    • Raymond, Deborah;
    • Doan, Nancy;
    • Bressman, Susan B.;
    • Marder, Karen S.;
    • Alcalay, Roy N.;
    • Rao, Ashwini K.;
    • Berg, Daniela;
    • Brockmann, Kathrin;
    • Aasly, Jan;
    • Waro, Bjørg Johanne;
    • Tolosa, Eduardo;
    • Vilas, Dolores;
    • Pont‐Sunyer, Claustre
    Publication type:
    journal article
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    Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene.

    Published in:
    Movement Disorders, 2015, v. 30, n. 7, p. 981, doi. 10.1002/mds.26213
    By:
    • Mirelman, Anat;
    • Alcalay, Roy N.;
    • Saunders‐Pullman, Rachel;
    • Yasinovsky, Kira;
    • Thaler, Avner;
    • Gurevich, Tanya;
    • Mejia‐Santana, Helen;
    • Raymond, Deborah;
    • Gana‐Weisz, Mali;
    • Bar‐Shira, Anat;
    • Ozelius, Laurie;
    • Clark, Lorraine;
    • Orr‐Urtreger, Avi;
    • Bressman, Susan;
    • Marder, Karen;
    • Giladi, Nir
    Publication type:
    Article
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    A cognitive fMRI study in non-manifesting LRRK2 and GBA carriers.

    Published in:
    Brain Structure & Function, 2017, v. 222, n. 3, p. 1207, doi. 10.1007/s00429-016-1271-4
    By:
    • Bregman, Noa;
    • Thaler, Avner;
    • Mirelman, Anat;
    • Helmich, Rick;
    • Gurevich, Tanya;
    • Orr-Urtreger, Avi;
    • Marder, Karen;
    • Bressman, Susan;
    • Bloem, Bastiaan;
    • Giladi, Nir
    Publication type:
    Article
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    Biochemical markers for severity and risk in GBA and LRRK2 Parkinson's disease.

    Published in:
    Journal of Neurology, 2021, v. 268, n. 4, p. 1517, doi. 10.1007/s00415-020-10325-4
    By:
    • Thaler, Avner;
    • Omer, Nurit;
    • Giladi, Nir;
    • Gurevich, Tanya;
    • Bar-Shira, Anat;
    • Gana-Weisz, Mali;
    • Goldstein, Orly;
    • Kestenbaum, Meir;
    • Cedarbaum, Jesse M.;
    • Orr-Urtreger, Avi;
    • Shenhar-Tsarfaty, Shani;
    • Mirelman, Anat
    Publication type:
    Article
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    Parkinson disease phenotype in Ashkenazi jews with and without LRRK2 G2019S mutations.

    Published in:
    Movement Disorders, 2013, v. 28, n. 14, p. 1966, doi. 10.1002/mds.25647
    By:
    • Alcalay, Roy N.;
    • Mirelman, Anat;
    • Saunders‐Pullman, Rachel;
    • Tang, Ming‐X;
    • Mejia Santana, Helen;
    • Raymond, Deborah;
    • Roos, Ernest;
    • Orbe‐Reilly, Martha;
    • Gurevich, Tanya;
    • Bar Shira, Anat;
    • Gana Weisz, Mali;
    • Yasinovsky, Kira;
    • Zalis, Maayan;
    • Thaler, Avner;
    • Deik, Andres;
    • Barrett, Matthew James;
    • Cabassa, Jose;
    • Groves, Mark;
    • Hunt, Ann L.;
    • Lubarr, Naomi
    Publication type:
    Article
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    Red flags for multiple system atrophy.

    Published in:
    Movement Disorders, 2008, v. 23, n. 8, p. 1093, doi. 10.1002/mds.21992
    By:
    • Köllensperger, Martin;
    • Geser, Felix;
    • Seppi, Klaus;
    • Stampfer-Kountchev, Michaela;
    • Sawires, Martin;
    • Scherfler, Christoph;
    • Boesch, Sylvia;
    • Mueller, Joerg;
    • Koukouni, Vasiliki;
    • Quinn, Niall;
    • Pellecchia, Maria Teresa;
    • Barone, Paolo;
    • Schimke, Nicole;
    • Dodel, Richard;
    • Oertel, Wolfgang;
    • Dupont, Erik;
    • Østergaard, Karen;
    • Daniels, Christine;
    • Deuschl, Günther;
    • Gurevich, Tanya
    Publication type:
    Article
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    Early Screening for the Parkinson Variant of Multiple System Atrophy: A 6‐Item Score.

    Published in:
    Movement Disorders Clinical Practice, 2024, v. 11, n. 7, p. 867, doi. 10.1002/mdc3.14048
    By:
    • Fanciulli, Alessandra;
    • Stankovic, Iva;
    • Avraham, Omer;
    • Jecmenica Lukic, Milica;
    • Ezra, Adi;
    • Leys, Fabian;
    • Goebel, Georg;
    • Krismer, Florian;
    • Petrovic, Igor;
    • Svetel, Marina;
    • Seppi, Klaus;
    • Kostic, Vladimir;
    • Giladi, Nir;
    • Poewe, Werner;
    • Wenning, Gregor K.;
    • Gurevich, Tanya
    Publication type:
    Article
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    R869C mutation in molecular motor KIF17 gene is involved in dementia with Lewy bodies.

    Published in:
    Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 2021, v. 13, n. 1, p. 1, doi. 10.1002/dad2.12143
    By:
    • Goldstein, Orly;
    • Gana‐Weisz, Mali;
    • Shiner, Tamara;
    • Attar, Reut;
    • Mordechai, Yael;
    • Waldman, Yedael Y.;
    • Bar‐Shira, Anat;
    • Thaler, Avner;
    • Gurevich, Tanya;
    • Mirelman, Anat;
    • Giladi, Nir;
    • Orr‐Urtreger, Avi
    Publication type:
    Article
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    Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 17, p. 4693, doi. 10.1093/hmg/ddu158
    By:
    • Vacic, Vladimir;
    • Ozelius, Laurie J.;
    • Clark, Lorraine N.;
    • Bar-Shira, Anat;
    • Gana-Weisz, Mali;
    • Gurevich, Tanya;
    • Gusev, Alexander;
    • Kedmi, Merav;
    • Kenny, Eimear E.;
    • Liu, Xinmin;
    • Mejia-Santana, Helen;
    • Mirelman, Anat;
    • Raymond, Deborah;
    • Saunders-Pullman, Rachel;
    • Desnick, Robert J.;
    • Atzmon, Gil;
    • Burns, Edward R.;
    • Ostrer, Harry;
    • Hakonarson, Hakon;
    • Bergman, Aviv
    Publication type:
    Article