MDS Abstracts

Abstracts from the International Congress of Parkinson’s and Movement Disorders.

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2017 International Congress

June 4-8, 2017. Vancouver, BC.

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Tuesday, June 6, 2017

1:45pm-3:15pm
Assessments of Movement Disorder Symptoms and Functional Impacts in Glucose Transporter Type 1 Deficiency Syndrome (Glut1 DS)

A. Bowden, S. Blair, K. Wesdock, M. Haller, M. Brandabur, P. Collins, A. Skrinar, J. Mayhew (Novato, CA, USA)

Rare Genetic and Metabolic Diseases  ·  Exhibit Hall C
1:45pm-3:15pm
Association analysis of single nucleotide polymorphisms near the DYT3 locus to dystonic symptoms in X-linked dystonia-parkinsonism

G. Saranza, D. Sumalapao, A. Domingo, P. Pasco, R.D. Jamora, L. Lee, A. Westenberger, C. Klein (Manila, Philippines)

Genetics (Non-PD)  ·  Exhibit Hall C
1:45pm-3:15pm
Association of CSF biomarkers with motor and non-motor features in moderately advanced Parkinson’s disease cohort: the BioFIND study

J. Goldman, A. Amara, L. Shaw, P. Taylor, H. Andrews, R. Alcalay, T. Xie, P. Tuite, C. Henchcliffe, P. Hogarth, S. Frank, M.-H. Saint Hilaire, A. Naito, M. Frasier, V. Arnedo, A. Reimer, M. Sutherland, C. Swanson-Fischer, K. Gwinn, U. Kang (Chicago, IL, USA)

Parkinson's Disease: Pathophysiology  ·  Exhibit Hall C
1:45pm-3:15pm
Ataxia and increased cerebrospinal fluid phosphate associated with a mutation in the SLC20A2 gene

M. Paucar, H. Almqvist, V. Jelic, G. Hagman, G. Jörneskog, S. Holmin, I. Björkhem, P. Svenningsson (Stockholm, Sweden)

Genetics (Non-PD)  ·  Exhibit Hall C
1:45pm-3:15pm
Atypical and slowly progressive FTDP-17 caused by MAPT p.R406W mutations – similarities to AD and PSP.

E. Ygland, D. van Westen, E. Englund, R. Rademakers, Z. Wszolek, K. Nilsson, C. Nilsson, O. Hansson, L. Gustafson, A. Puschmann (Lund, Sweden)

Rare Genetic and Metabolic Diseases  ·  Exhibit Hall C
1:45pm-3:15pm
Autonomous Tracking of Body Bradykinesia during Unconstrained Activities in Parkinson’s Disease

S. Roy, B. Shiwani, J. Kline, M. Saint-Hilaire, C. Thomas, M. Gennert, G. De Luca (Natick, MA, USA)

Technology  ·  Exhibit Hall C
1:45pm-3:15pm
Axial signs in early-stage Parkinson’s disease :  an influence of the genotype ?

G. BAILLE, D. DEVOS, V. HUIN, T. PEREZ, B. SABLONNIERE, L. DEFEBVRE, C. MOREAU (CHRU Lille, France)

Parkinson's Disease: Pathophysiology  ·  Exhibit Hall C
1:45pm-3:15pm
Barriers to exercise in newly diagnosed Parkinson’s disease

I. Argyropoulos, E. Pearson, F. Murphy, V. Queen, J. Rideout, C. Carrollq (Plymouth, United Kingdom)

Therapy in Movement Disorders  ·  Exhibit Hall C
1:45pm-3:15pm
Baseline multimodal information predicts future motor impairment in premanifest Huntington’s disease

E. Castro, P. Polosecki, I. Rish, G. Cecchi (Yorktown Heights, NY, USA)

Huntington's Disease  ·  Exhibit Hall C
1:45pm-3:15pm
Behavioral Changes on the UCSD Huntington’s Disease Behavioral Questionnaire (HD-BQ) Distinguish Patients Transitioning to Manifest Huntington’s disease (HD)

S. Park, S. Nam, A. Nathan, A. Haque, A. Haque, P. Gilbert, J. Corey-Bloom (La Jolla, CA, USA)

Huntington's Disease  ·  Exhibit Hall C
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