Resultats de la cerca - Rachel Saunders‐Pullman
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LRRK2 and GBA Variants Exert Distinct Influences on Parkinson’s Disease-Specific Metabolic Networks per Katharina A. Schindlbeck, An Vo, Nha Nguyen, Chris C. Tang, Martin Niethammer, Vijay Dhawan, Vicky Brandt, Rachel Saunders‐Pullman, Susan Bressman, David Eidelberg
Publicat 2019Artigo -
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<i>LRRK2</i> G2019S mutations are associated with an increased cancer risk in Parkinson disease per Rachel Saunders‐Pullman, Matthew J. Barrett, Kaili Stanley, Marta San Luciano, Vicki Shanker, Lawrence Severt, Ann Hunt, Deborah Raymond, Laurie J. Ozelius, Susan Bressman
Publicat 2010Artigo -
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Digitized Spiral Drawing: A Possible Biomarker for Early Parkinson’s Disease per 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
Publicat 2016Artigo -
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Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition per 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
Publicat 2019Artigo -
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<i>LRRK2</i>G2019S as a Cause of Parkinson's Disease in Ashkenazi Jews per 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
Publicat 2006Carta -
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Neuropsychological performance in LRRK2 G2019S carriers with Parkinson's disease per 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
Publicat 2014Artigo -
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Higher Frequency of Certain Cancers in<i>LRRK2</i>G2019S Mutation Carriers With Parkinson Disease per 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
Publicat 2014Artigo -
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Gaucher disease ascertained through a Parkinson's center: Imaging and clinical characterization per 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
Publicat 2010Artigo -
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Progression in the <i>LRRK2</i>-Associated Parkinson Disease Population per 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
Publicat 2018Artigo -
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Association of Dual <i>LRRK2 </i>G2019S and <i>GBA</i> Variations With Parkinson Disease Progression per 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
Publicat 2021Artigo -
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The p.L302P mutation in the lysosomal enzyme gene <i>SMPD1</i> is a risk factor for Parkinson disease per 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
Publicat 2013Artigo -
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Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the <i>LRRK2</i> gene per 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
Publicat 2015Artigo -
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Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian Mennonites per 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
Publicat 2012Artigo -
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Psychiatric disorders, myoclonus dystonia and <i> <scp>SGCE</scp> </i> : an international study per 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
Publicat 2015Artigo
Eines de cerca:
Matèries relacionades
Medicine
Disease
Internal medicine
Parkinson's disease
Biology
Genetics
Gene
Psychiatry
Psychology
LRRK2
Mutation
Neuroscience
Cohort
Dystonia
Pathology
Environmental health
Genotype
Movement disorders
Phenotype
Population
Oncology
Cognition
Depression (economics)
Economics
Macroeconomics
Montreal Cognitive Assessment
Penetrance
Physical medicine and rehabilitation
Allele
Anxiety