Torthaí cuardaigh - Tanya Gurevich

Beachtaigh na torthaí
  1. 1
    COVID-19 mRNA Vaccination

    COVID-19 mRNA Vaccination de réir Vered, Livneh, Lubov, Barsky, Adi, Ezra, Tanya, Gurevich

    Foilsithe / Cruthaithe 2022
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  2. 2
    Quality of life in Parkinson's disease: A gender‐specific perspective

    Quality of life in Parkinson's disease: A gender‐specific perspective de réir Yacov Balash, Amos D. Korczyn, Angel A. Migirov, Tanya Gurevich

    Foilsithe / Cruthaithe 2019
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  3. 3
    Disorders of the Oral Cavity in Parkinson’s Disease and Parkinsonian Syndromes

    Disorders of the Oral Cavity in Parkinson’s Disease and Parkinsonian Syndromes de réir Yair Zlotnik, Yacov Balash, Amos D. Korczyn, Nir Giladi, Tanya Gurevich

    Foilsithe / Cruthaithe 2015
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  4. 4
    Subjective memory complaints in elders: depression, anxiety, or cognitive decline?

    Subjective memory complaints in elders: depression, anxiety, or cognitive decline? de réir Yacov Balash, M. Mordechovich, H. Shabtai, Nir Giladi, Tanya Gurevich, Amos D. Korczyn

    Foilsithe / Cruthaithe 2012
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  5. 5
    Rivastigmine (Exelon) for dementia in patients with Parkinson's disease

    Rivastigmine (Exelon) for dementia in patients with Parkinson's disease de réir Nir Giladi, H. Shabtai, Tanya Gurevich, B. R. Benbunan, M. Anca, Amos D. Korczyn

    Foilsithe / Cruthaithe 2003
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  6. 6
    Gait alterations in healthy carriers of the LRRK2 G2019S mutation

    Gait alterations in healthy carriers of the LRRK2 G2019S mutation de réir Anat Mirelman, Tanya Gurevich, Nir Giladi, Anat Bar‐Shira, Avi Orr‐Urtreger, Jeffrey M. Hausdorff

    Foilsithe / Cruthaithe 2011
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  7. 7
    White Matter Hyperintensities in Parkinson’s Disease: Do They Explain the Disparity between the Postural Instability Gait Difficulty and Tremor Dominant Subtypes?

    White Matter Hyperintensities in Parkinson’s Disease: Do They Explain the Disparity between the Postural Instability Gait Difficulty and Tremor Dominant Subtypes? de réir Talia Herman, Keren Rosenberg‐Katz, Yael Jacob, Eitan Auriel, Tanya Gurevich, Nir Giladi, Jeffrey M. Hausdorff

    Foilsithe / Cruthaithe 2013
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  8. 8
    ND0612 (levodopa/carbidopa for subcutaneous infusion) in patients with Parkinson's disease and motor response fluctuations: A randomized, placebo-controlled phase 2 study

    ND0612 (levodopa/carbidopa for subcutaneous infusion) in patients with Parkinson's disease and motor response fluctuations: A randomized, placebo-controlled phase 2 study de réir Nir Giladi, Tanya Gurevich, Ruth Djaldetti, Liat Adar, Ryan Case, Shelly Leibman-Barak, Noah J. Sasson, Yoseph Caraco

    Foilsithe / Cruthaithe 2021
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  9. 9
    High Frequency of <i>GBA</i> Gene Mutations in Dementia With Lewy Bodies Among Ashkenazi Jews

    High Frequency of <i>GBA</i> Gene Mutations in Dementia With Lewy Bodies Among Ashkenazi Jews de réir Tamara Shiner, Anat Mirelman, Mali Gana Weisz, Anat Bar‐Shira, Elissa L. Ash, Ron Cialic, Naomi Nevler, Tanya Gurevich, Noa Bregman, Avi Orr‐Urtreger, Nir Giladi

    Foilsithe / Cruthaithe 2016
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  10. 10
    Concomitant Medication Usage with <scp>Levodopa‐Carbidopa</scp> Intestinal Gel: Results from the <scp>COSMOS</scp> Study

    Concomitant Medication Usage with <scp>Levodopa‐Carbidopa</scp> Intestinal Gel: Results from the <scp>COSMOS</scp> Study de réir Alfonso Fasano, Tanya Gurevich, Robert Jech, Norbert Kovács, Per Svenningsson, József Attila Szász, Juan Carlos Parra, Lars Bergmann, Anita Johnson, O. Sánchez-Soliño, Zhongwen Tang, Lydia Vela

    Foilsithe / Cruthaithe 2021
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  11. 11
    The effect of polygenic risk score on PD risk and phenotype in <i>LRRK2</i> G2019S and <i>GBA1</i> carriers

    The effect of polygenic risk score on PD risk and phenotype in <i>LRRK2</i> G2019S and <i>GBA1</i> carriers de réir Orly Goldstein, Shachar Shani, Mali Gana‐Weisz, Nadav Elkoshi, Fergal Casey, Yu Sun, Khyati Chandratre, Jesse M. Cedarbaum, Cornelis Blauwendraat, Anat Bar‐Shira, Avner Thaler, Tanya Gurevich, Anat Mirelman, Nir Giladi, Avi Orr‐Urtreger, Roy N. Alcalay

    Foilsithe / Cruthaithe 2025
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  12. 12
    The p.L302P mutation in the lysosomal enzyme gene <i>SMPD1</i> is a risk factor for Parkinson disease

    The p.L302P mutation in the lysosomal enzyme gene <i>SMPD1</i> is a risk factor for Parkinson disease de réir Ziv Gan‐Or, Laurie J. Ozelius, Anat Bar‐Shira, Rachel Saunders‐Pullman, Anat Mirelman, Ruth Kornreich, Mali Gana‐Weisz, Deborah Raymond, Liron Rozenkrantz, Andres Deik, Tanya Gurevich, Susan J. Gross, Nicole Schreiber‐Agus, Nir Giladi, Susan Bressman, Avi Orr‐Urtreger

    Foilsithe / Cruthaithe 2013
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  13. 13
    Tossing and Turning in Bed: Nocturnal Movements in Parkinson's Disease

    Tossing and Turning in Bed: Nocturnal Movements in Parkinson's Disease de réir Anat Mirelman, Inbar Hillel, Lynn Rochester, Silvia Del Din, Bastiaan R. Bloem, Laura Avanzino, Alice Nieuwboer, Inbal Maidan, Talia Herman, Avner Thaler, Tanya Gurevich, Meir Kestenbaum, Avi Orr‐Urtreger, Mirosław Bryś, Jesse M. Cedarbaum, Nir Giladi, Jeffrey M. Hausdorff

    Foilsithe / Cruthaithe 2020
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  14. 14
    Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the <i>LRRK2</i> gene

    Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the <i>LRRK2</i> gene de réir Anat Mirelman, Roy N. Alcalay, Rachel Saunders‐Pullman, Kira Yasinovsky, Avner Thaler, Tanya Gurevich, Helen Mejia‐Santana, Deborah Raymond, Mali Gana‐Weisz, Anat Bar‐Shira, Laurie J. Ozelius, Lorraine N. Clark, Avi Orr‐Urtreger, Susan Bressman, Karen Marder, Nir Giladi

    Foilsithe / Cruthaithe 2015
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  15. 15
    Application of the Movement Disorder Society prodromal criteria in healthy <i>G2019S</i>‐<i>LRRK2</i> carriers

    Application of the Movement Disorder Society prodromal criteria in healthy <i>G2019S</i>‐<i>LRRK2</i> carriers de réir Anat Mirelman, Rachel Saunders‐Pullman, Roy N. Alcalay, Shiran Shustak, Avner Thaler, Tanya Gurevich, Deborah Raymond, Helen Mejia‐Santana, Martha Orbe Reilly, Laurie J. Ozelius, Lorraine N. Clark, Mali Gana‐Weisz, Anat Bar‐Shira, Avi Orr‐Utreger, Susan Bressman, Karen Marder, Nir Giladi

    Foilsithe / Cruthaithe 2018
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  16. 16
    Arm swing as a potential new prodromal marker of Parkinson's disease

    Arm swing as a potential new prodromal marker of Parkinson's disease de réir Anat Mirelman, Hagar Bernad‐Elazari, Avner Thaler, Eytan Giladi‐Yacobi, Tanya Gurevich, Mali Gana‐Weisz, Rachel Saunders‐Pullman, Deborah Raymond, Nancy Doan, Susan Bressman, Karen Marder, Roy N. Alcalay, Ashwini K. Rao, Daniela Berg, Kathrin Brockmann, Jan Aasly, Bjørg Warø, Eduardo Tolosa, Dolores Vilas, Claustre Pont‐Sunyer, Avi Orr‐Urtreger, Jeffrey M. Hausdorff, Nir Giladi

    Foilsithe / Cruthaithe 2016
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  17. 17
    Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes

    Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes de réir Vladimir Vacic, Laurie J. Ozelius, Lorraine N. Clark, Anat Bar‐Shira, Mali Gana‐Weisz, Tanya Gurevich, Alexander Gusev, Merav Kedmi, Eimear E. Kenny, X. Liu, Helen Mejia‐Santana, Anat Mirelman, Deborah Raymond, Rachel Saunders‐Pullman, Robert J. Desnick, Gil Atzmon, E. Robert Burns, Harry Ostrer, Hákon Hákonarson, Aviv Bergman, Nir Barzilai, Ariel Darvasi, Inga Peter, Saurav Guha, Todd Lencz, Nir Giladi, K. Marder, I. Pe'er, Susan Bressman, Avi Orr‐Urtreger

    Foilsithe / Cruthaithe 2014
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  18. 18
    Red flags for multiple system atrophy

    Red flags for multiple system atrophy de réir Martin Köllensperger, Felix Geser, Klaus Seppi, Michaela Stampfer‐Kountchev, Martin Sawires, Christoph Scherfler, Sylvia Boesch, Joerg Mueller, Vasiliki Koukouni, Niall Quinn, Maria Teresa Pellecchia, Paolo Barone, Nicole Schimke, Richard Dodel, Wolfgang H. Oertel, E. Dupont, Karen Østergaard, Christine Daniels, Günther Deuschl, Tanya Gurevich, Nir Giladi, Miguel Coelho, Cristina Sampaio, Christer Nilsson, Håkan Widner, Francesca Del Sorbo, Alberto Albanese, Adriana Cardozo, Eduardo Tolosa, Michael Abele, Thomas Klockgether, Christoph Kamm, Thomas Gasser, Ruth Djaldetti, Carlo Colosimo, G. Meco, Anette Schrag, Werner Poewe, Gregor K. Wenning

    Foilsithe / Cruthaithe 2008
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  19. 19
    The natural history of multiple system atrophy: a prospective European cohort study

    The natural history of multiple system atrophy: a prospective European cohort study de réir Gregor K. Wenning, Felix Geser, Florian Krismer, Klaus Seppi, Susanne Duerr, Sylvia Boesch, Martin Köllensperger, Hans H. Goebel, Karl Pfeiffer, Paolo Barone, Maria Teresa Pellecchia, Niall Quinn, Vasiliki Koukouni, Clare J. Fowler, Anette Schrag, Christopher J. Mathias, Nir Giladi, Tanya Gurevich, E. Dupont, Karen Østergaard, Christer Nilsson, Håkan Widner, Wolfgang H. Oertel, Karla Eggert, Alberto Albanese, Francesca Del Sorbo, Eduardo Tolosa, Adriana Cardozo, Günther Deuschl, Helge Hellriegel, Thomas Klockgether, Richard Dodel, Cristina Sampaio, Miguel Coelho, Ruth Djaldetti, Eldad Melamed, Thomas Gasser, Christoph Kamm, G. Meco, Carlo Colosimo, Olivier Rascol, Wassilios G. Meissner, François Tison, Werner Poewe

    Foilsithe / Cruthaithe 2013
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  20. 20
    Parkinson disease phenotype in Ashkenazi jews with and without <i>LRRK2</i> G2019S mutations

    Parkinson disease phenotype in Ashkenazi jews with and without <i>LRRK2</i> G2019S mutations de réir Roy N. Alcalay, Anat Mirelman, Rachel Saunders‐Pullman, Ming‐X Tang, Helen Mejia Santana, Deborah Raymond, Ernest Roos, Martha Orbe‐Reilly, Tanya Gurevich, Anat Bar Shira, Mali Gana Weisz, Kira Yasinovsky, Maayan Zalis, Avner Thaler, Andres Deik, Matthew J. Barrett, Jose Cabassa, Mark Groves, Ann Hunt, Naomi Lubarr, Marta San Luciano, Joan Miravite, Christina A. Palmese, Rivka Sachdev, Harini Sarva, Lawrence Severt, Vicki Shanker, Matthew Swan, Jeannie Soto‐Valencia, Brooke Johannes, Robert Ortega, Stanley Fahn, Lucien Côté, Cheryl Waters, Pietro Mazzoni, Blair Ford, Elan D. Louis, Oren Levy, Llency Rosado, Dylanis Lopez Ruiz, Tsvyatko Dorovski, Michael W. Pauciulo, William C. Nichols, Avi Orr‐Urtreger, Laurie J. Ozelius, Lorraine N. Clark, Nir Giladi, Susan Bressman, Karen Marder

    Foilsithe / Cruthaithe 2013
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