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DaT-uptake z-scores for Caudate and Striatum Predict Levodopa Requirement in Early Parkinson’s Disease

Author:Rukavina, Katarina   Mulholland, Nicola   Corcoran, Ben   Staunton, Juliet   Krbot Skoric, Magdalena   Rota, Silvia   Rizos, Alexandra   Ray Chaudhuri, K   

Session Name:S37: Movement Disorders: Phenotyping and Biomarkers  

Topic:Movement Disorders  

Program Number:S37.009  

Author Institution:King's College London, London, United Kingdom  King's College Hospital , London, United Kingdom  King's College Hospital, London, United Kingdom  University Zagreb School of Medicine, Zagreb, Croatia  King's College Hospital, London, UK, London, United Kingdom  

Automated Audio Analysis of Dysarthria in Huntington’s disease (Audio-HD)

Author:Sierra, Luis   Hildebrand, Karen   Ullman, Clementina   Mwangi, Magdaline   O'Connell, Henry   Frank, Samuel   Laganiere, Simon   

Session Name:S37: Movement Disorders: Phenotyping and Biomarkers  

Topic:Movement Disorders  

Program Number:S37.010  

Author Institution:Beth Israel Deaconess Medical Center, Boston, MA  Canary Speech, Provo, UT  

Identification of candidate Parkinson’s disease predisposition genes in high-risk pedigrees

Author:Moretti, Paolo   Figueroa, Karla   Pulst, stefan   Dotti, Alessandro   Stevens, Jeff   Allen-Brady, Kristina   Cannon-Albright, Lisa   

Session Name:S42: Movement Disorders: Genetics and Risk Modifiers  

Topic:Movement Disorders  

Program Number:S42.001  

Author Institution:University of Utah, Salt Lake City, UT  Midwestern University, Downers Grove, IL  

Frequency of Known Genetic Variants for Parkinson’s Disease in the PD GENEration Study Cohort

Author:Beck, James   Ghosh Galvelis, Kamalini   Nance, Martha   Naito, Anna   Mencacci, Niccolo   Mata, Ignacio   Hall, Anne   Schulze, Jeanine   Hodges, Rayza Priscila   Wills, Anne Marie   Schwarzschild, Michael   Marder, Karen   Simuni, Tanya   Miller, Mandy   Verbrugge, Jennifer   Cook, Lola   Heathers, Laura   Totten, Michelle   Foroud, Tatiana   Alcalay, Roy   

Session Name:S42: Movement Disorders: Genetics and Risk Modifiers  

Topic:Movement Disorders  

Program Number:S42.002  

Author Institution:Parkinson's Foundation, New York, NY  Park Nicollet Clinic, Golden Valley, MN  Parkinson's Foundation, Miami, FL  Northwestern University, Chicago, IL  Cleveland Clinic Foundation, Cleveland, OH  Parkinson's Foundation, Walnut, CA  Indiana University School of Medicine, Indianapolis, IN  Indiana University, Indianapolis, IN  MGH, Boston, MA  Massachusetts General Hospital, Boston, MA  Columbia University, New York, NY  Northwestern University Feinberg School of Medicien, Chicago, IL  

Understanding how GBA mutations influence Parkinson’s disease progression

Author:Khera, Arnav   Fish, Sarah   Estes, Raja   Yu, Selina   Pallanck, Leo   Young, Jessica   Davis, Marie   

Session Name:S42: Movement Disorders: Genetics and Risk Modifiers  

Topic:Movement Disorders  

Program Number:S42.003  

Author Institution:VA Puget Sound, Sammamish, WA  VA Puget Sound, Seattle, WA  VA Puget Sound Health Care System , Seattle, WA  Department of Genome Sciences, University of Washington, Seattle, WA  Institute for Stem Cell Regenerative Medicine, University of Washington, Seattle, WA