MDS Abstracts

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

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2019 International Congress

September 22-26, 2019. Nice, France.

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Monday, September 23, 2019

1:45pm-3:15pm
Gene panel testing in movement disorders: an efficient approach highlighting overlaps and heterogeneity

S. Montaut, C. Tranchant, N. Drouot, G. Rudolf, C. Guissart, J. Tarabeux, T. Stemmelen, A. Velt, C. Fourrage, P. Nitschke, B. Gerard, JL. Mandel, M. Koenig, J. Chelly, M. Anheim (Paris, France)

Genetics  ·  Les Muses Terrace, Level 3
1:45pm-3:15pm
Generalised Polymyoclonus In a Patient With Central Nervous System Tuberculosis

K. Shahedah, MS. Mohamad Salmi (Pahang, Malaysia)

Myoclonus  ·  Les Muses, Level 3
1:45pm-3:15pm
Genetic analysis of DNA methylation and hydroxymethylation genes in Parkinson’s disease

L. Qin, L. Shu, B. Tang, Q. Xu (Changsha, China)

Genetics  ·  Les Muses Terrace, Level 3
1:45pm-3:15pm
Genetic diagnosis of Chorea-acanthocytosis using whole exome sequencing revealed novel VPS13A Gene mutation

H. Ryu, C. Hong, J. Lee (Daegu, Republic of Korea)

Choreas (Non-Huntington’s Disease)  ·  Les Muses, Level 3
1:45pm-3:15pm
Genetic markers revealed in dysregulated pathways in ischemic stroke may lead to Parkinson’s disease

H. Singh, V. Swarup, A. Srivastava (Marseille, France)

Genetics  ·  Les Muses Terrace, Level 3
1:45pm-3:15pm
Genetic panel testing in Parkinson’s disease

T. Toomsoo, I. Rubanovich, I. Kalju, S. Ott, A. Lindmäe, M. Mällo, K. Jaakson, K. Joost, K. Vender (Tallinn, Estonia)

Genetics  ·  Les Muses Terrace, Level 3
1:45pm-3:15pm
Genetic polymorphism (rs6971) in translocator protein (TSPO) and its clinical relevance in Parkinson’s disease

P. Surathi, M. Matarazzo, A. Sethi, J. Mckenzie, N. Neilson, R. Ross, M. Schulzer, M. Farrer, S. Booromand, J. Stoessl (Vancouver, BC, Canada)

Genetics  ·  Les Muses Terrace, Level 3
1:45pm-3:15pm
Genetic study of patients with Parkinson’s disease subjected to second line therapies

F. Carrillo, S. Jesus, T. Periñan, R. Escuela, D. Buiza, MA. Labrador, M. Carrión, A. Adarmes, D. Macias, P. Gomez-Garre, P. Mir (Seville, Spain)

Genetics  ·  Les Muses Terrace, Level 3
1:45pm-3:15pm
Genetics of Parkinson’s in India – Young Onset Parkinson’s Disease (GOPI-YOPD) – A Preliminary Demographic profile

P. Kukkle, V. Goyal, R. Kandadai, R. Borgohain, H. Kumar, A. Mukherjee, A. Biswas, S. Das, U. Muthane, S. Desai, P. Wadia, P. Pal, R. Yadav, V. Ramprasad (Bangalore, India)

Other  ·  Agora 2 West, Level 2
1:45pm-3:15pm
Genotype-Phenotype correlations of Episodic Ataxia (EA). MDSGene Systematic Review

A. Shetty, K. Nabieva, F. Zeldenrust, A. Rasheed, J. Huang, S. Petkovic, K. Lohmann, C. Klein, C. Marras, O. Waln (Lübeck, Germany)

Ataxia  ·  Les Muses, Level 3
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