Torthaí cuardaigh - Rachel Saunders‐Pullman

Beachtaigh na torthaí
  1. 1
    Substance Abuse and Movement Disorders: Complex Interactions and Comorbidities

    Substance Abuse and Movement Disorders: Complex Interactions and Comorbidities de réir Andres Deik, Rachel Saunders‐Pullman, Marta San Luciano

    Foilsithe / Cruthaithe 2012
    Faigh an téacs iomlán
    Revisão
    Cuir le mo chuid Ceanán
    Sábháilte in:
  2. 2
    Diagnosis and Referral Delay in Women With Parkinson's Disease

    Diagnosis and Referral Delay in Women With Parkinson's Disease de réir Rachel Saunders‐Pullman, Cuiling Wang, Kaili Stanley, Susan Bressman

    Foilsithe / Cruthaithe 2011
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  3. 3
    Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study

    Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study de réir Susan Bressman, Deborah Raymond, Tania Fuchs, Gary A. Heiman, Laurie J. Ozelius, Rachel Saunders‐Pullman

    Foilsithe / Cruthaithe 2009
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  4. 4
    Metabolic changes in <i>DYT11</i> myoclonus-dystonia

    Metabolic changes in <i>DYT11</i> myoclonus-dystonia de réir Maren Carbon, Deborah Raymond, Laurie J. Ozelius, Rachel Saunders‐Pullman, Steven J. Frucht, Vijay Dhawan, Susan Bressman, David Eidelberg

    Foilsithe / Cruthaithe 2013
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  5. 5
    LRRK2 and GBA Variants Exert Distinct Influences on Parkinson’s Disease-Specific Metabolic Networks

    LRRK2 and GBA Variants Exert Distinct Influences on Parkinson’s Disease-Specific Metabolic Networks de réir Katharina A. Schindlbeck, An Vo, Nha Nguyen, Chris C. Tang, Martin Niethammer, Vijay Dhawan, Vicky Brandt, Rachel Saunders‐Pullman, Susan Bressman, David Eidelberg

    Foilsithe / Cruthaithe 2019
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  6. 6
    <i>LRRK2</i> G2019S mutations are associated with an increased cancer risk in Parkinson disease

    <i>LRRK2</i> G2019S mutations are associated with an increased cancer risk in Parkinson disease de réir Rachel Saunders‐Pullman, Matthew J. Barrett, Kaili Stanley, Marta San Luciano, Vicki Shanker, Lawrence Severt, Ann Hunt, Deborah Raymond, Laurie J. Ozelius, Susan Bressman

    Foilsithe / Cruthaithe 2010
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  7. 7
    Digitized Spiral Drawing: A Possible Biomarker for Early Parkinson’s Disease

    Digitized Spiral Drawing: A Possible Biomarker for Early Parkinson’s Disease de réir Marta San Luciano, Cuiling Wang, Roberto A. Ortega, Qiping Yu, Sarah Boschung, Jeannie Soto‐Valencia, Susan Bressman, Richard B. Lipton, Seth L. Pullman, Rachel Saunders‐Pullman

    Foilsithe / Cruthaithe 2016
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  8. 8
    Olfactory dysfunction in <i>LRRK2</i> G2019S mutation carriers

    Olfactory dysfunction in <i>LRRK2</i> G2019S mutation carriers de réir Rachel Saunders‐Pullman, Kaili Stanley, C. Wang, Marta San Luciano, Vicki Shanker, Amelia R. Hunt, Lawrence Severt, Deborah Raymond, Laurie J. Ozelius, Richard B. Lipton, Susan Bressman

    Foilsithe / Cruthaithe 2011
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  9. 9
    Etiology of musician’s dystonia

    Etiology of musician’s dystonia de réir Alexander Schmidt, H.‐C. Jabusch, Eckart Altenmüller, J. Hagenah, Norbert Brüggemann, Katja Lohmann, Leonie Enders, P. L. Kramer, Rachel Saunders‐Pullman, Susan Bressman, Alexander Münchau, Christine Klein

    Foilsithe / Cruthaithe 2009
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  10. 10
    Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition

    Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition de réir Elena Arystarkhova, Ihtsham Haq, Timothy Luebbert, Fanny Mochel, Rachel Saunders‐Pullman, Susan Bressman, Polina Feschenko, Cynthia Salazar, Jared Cook, Scott Demarest, Allison Brashear, Laurie J. Ozelius, Kathleen J. Sweadner

    Foilsithe / Cruthaithe 2019
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  11. 11
    <i>LRRK2</i>G2019S as a Cause of Parkinson's Disease in Ashkenazi Jews

    <i>LRRK2</i>G2019S as a Cause of Parkinson's Disease in Ashkenazi Jews de réir Laurie J. Ozelius, Geetha Senthil, Rachel Saunders‐Pullman, Erin Ohmann, Amanda Deligtisch, Michele Tagliati, Ann Hunt, Christine Klein, Brian S. Henick, Susan M. Hailpern, Richard B. Lipton, Jeannie Soto‐Valencia, Neil Risch, Susan Bressman

    Foilsithe / Cruthaithe 2006
    Faigh an téacs iomlán Faigh an téacs iomlán
    Carta
    Cuir le mo chuid Ceanán
    Sábháilte in:
  12. 12
    Neuropsychological performance in LRRK2 G2019S carriers with Parkinson's disease

    Neuropsychological performance in LRRK2 G2019S carriers with Parkinson's disease de réir Roy N. Alcalay, Helen Mejia‐Santana, Anat Mirelman, Rachel Saunders‐Pullman, Deborah Raymond, Christina A. Palmese, Elise Caccappolo, Laurie J. Ozelius, Avi Orr‐Urtreger, Lorraine N. Clark, Nir Giladi, Susan Bressman, Karen Marder

    Foilsithe / Cruthaithe 2014
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  13. 13
    Higher Frequency of Certain Cancers in<i>LRRK2</i>G2019S Mutation Carriers With Parkinson Disease

    Higher Frequency of Certain Cancers in<i>LRRK2</i>G2019S Mutation Carriers With Parkinson Disease de réir Ilir Agalliu, Marta San Luciano, Anat Mirelman, Nir Giladi, Bjørg Warø, Jan Aasly, Rivka Inzelberg, Sharon Hassin‐Baer, Eitan Friedman, Javier Ruiz‐Martínez, J.F. Martí-Massó, Avi Orr‐Urtreger, Susan Bressman, Rachel Saunders‐Pullman

    Foilsithe / Cruthaithe 2014
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  14. 14
    Gaucher disease ascertained through a Parkinson's center: Imaging and clinical characterization

    Gaucher disease ascertained through a Parkinson's center: Imaging and clinical characterization de réir Rachel Saunders‐Pullman, Johann Hagenah, Vijay Dhawan, Kaili Stanley, Gregory M. Pastores, Swati Sathe, Michele Tagliati, Kelly A. Condefer, Christina A. Palmese, Norbert Brüggemann, Christine Klein, AM Roe, Ruth Kornreich, Laurie J. Ozelius, Susan Bressman

    Foilsithe / Cruthaithe 2010
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  15. 15
    Progression in the <i>LRRK2</i>-Associated Parkinson Disease Population

    Progression in the <i>LRRK2</i>-Associated Parkinson Disease Population de réir Rachel Saunders‐Pullman, Anat Mirelman, Roy N. Alcalay, Cuiling Wang, Roberto A. Ortega, Deborah Raymond, Helen Mejia‐Santana, Martha Orbe‐Reilly, Brooke Johannes, Avner Thaler, Laurie J. Ozelius, Avi Orr‐Urtreger, Karen Marder, Nir Giladi, Susan Bressman

    Foilsithe / Cruthaithe 2018
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  16. 16
    Association of Dual <i>LRRK2 </i>G2019S and <i>GBA</i> Variations With Parkinson Disease Progression

    Association of Dual <i>LRRK2 </i>G2019S and <i>GBA</i> Variations With Parkinson Disease Progression de réir Roberto A. Ortega, Cuiling Wang, Deborah Raymond, Nicole Bryant, Clemens R. Scherzer, Avner Thaler, Roy N. Alcalay, Andrew B. West, Anat Mirelman, Yuliya I. Kuras, Karen Marder, Nir Giladi, Laurie J. Ozelius, Susan Bressman, Rachel Saunders‐Pullman

    Foilsithe / Cruthaithe 2021
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  17. 17
    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
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  18. 18
    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
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  19. 19
    Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian Mennonites

    Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian Mennonites de réir Rachel Saunders‐Pullman, Deborah Raymond, A. Jon Stoessl, Douglas E. Hobson, Toshitaka Nakamura, Seth L. Pullman, D Lefton, Michael S. Okun, Ryan J. Uitti, Rivka Sachdev, Kaili Stanley, Marta San Luciano, J. Hagenah, Richard A. Gatti, Laurie J. Ozelius, Susan Bressman

    Foilsithe / Cruthaithe 2012
    Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:
  20. 20
    Psychiatric disorders, myoclonus dystonia and <i> <scp>SGCE</scp> </i> : an international study

    Psychiatric disorders, myoclonus dystonia and <i> <scp>SGCE</scp> </i> : an international study de réir Kathryn J. Peall, Joke M. Dijk, Rachel Saunders‐Pullman, Yasmine E. M. Dreissen, Ilke Loon, Daniëlle C. Cath, Manju A. Kurian, Michael J. Owen, E.M.J. Foncke, Huw R. Morris, Thomas Gasser, Susan Bressman, Friedrich Asmus, Marina A.J. Tijssen

    Foilsithe / Cruthaithe 2015
    Faigh an téacs iomlán Faigh an téacs iomlán
    Artigo
    Cuir le mo chuid Ceanán
    Sábháilte in:

Uirlisí cuardaigh: