2019 International Congress

September 22-26, 2019. Nice, France.

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Monday, September 23, 2019

1:45pm-3:15pm: Homozygous BZRAP1 mutations cause autosomal recessive dystonia

NE. Mencacci, MM. Brockmann, S. Pajusalu, B. Atasu, P. Gonzalez-Latapi, M. Schwake, B. Balint, A. Papandreou, A. Pittman, J. Simon-Sanchez, S. Wiethoff, TT. Warner, T. Gasser, M. Kurian, E. Lohmann, K. õunap, KP. Bhatia, C. Rosenmund, T. Sudhof, NW. Wood, D. Krainc, C. Acuna Goycolea (Chicago, IL, USA)

Genetics · Les Muses Terrace, Level 3

1:45pm-3:15pm: Homozygous Huntington’s disease with two reduced penetrance alleles: A Case Report

K. Grimm, C. Zühlke, C. Gerloff, S. Zittel (Hamburg, Germany)

Huntington’s Disease · Agora 3 West, Level 3

1:45pm-3:15pm: Huntington Disease-Like 2: A Case Presentation and Review of the Literature

J. Pleen, V. Saini, N. Doher, R. Walker, V. Singh (Kansas City, KS, USA)

Choreas (Non-Huntington’s Disease) · Les Muses, Level 3

1:45pm-3:15pm: Huntington’s Disease Protein Huntingtin Associates with its own mRNA

M. Rakhimova, M. Daropova (Tashkent, Uzbekistan)

Huntington’s Disease · Agora 3 West, Level 3

1:45pm-3:15pm: Huntington’s Disease presenting as sporadic cerebellar ataxia

GLF. Franklin, FAN. Nascimento, GMP. Pavanelli, SSM. Milano, HAT. Teive, NSL. Lima, SR. Raskin (Curitiba, Brazil)

Ataxia · Les Muses, Level 3

1:45pm-3:15pm: Huntington’s disease: A case review of Sub-Saharan Africans with diverse origins

M. Muthinja, J. Hooker (Nairobi, Kenya)

Huntington’s Disease · Agora 3 West, Level 3

1:45pm-3:15pm: Hydralazine protects nigrostriatal dopaminergic neurons from MPP+ and MPTP induced neurotoxicity: Roles of Nrf2-ARE signaling pathway

XF. Guo, T. Wang, J. Huang, N. Xiong, C. Han, K. Ma, Y. Xia, F. Wan, JJ. Hu, SJ. Yin, L. Kou, YD. Sun, JW. Wu (Wuhan, China)

Neuropharmacology · Les Muses Terrace, Level 3

1:45pm-3:15pm: Hyperammonemic Encephalopathy as Primary Cause of Movement Disorders: Report of Two Cases

G. Fabiani, FMB. Germiniani, S. Raskin, HAG. Teive (Curitiba, Brazil)

Rare Genetic and Metabolic Diseases · Les Muses Terrace, Level 3

1:45pm-3:15pm: Hyperkinetic Movement Disorders in Congenital Disorders of Glycosylation

G. Mostile, R. Barone, A. Nicoletti, R. Rizzo, D. Martinelli, L. Sturiale, A. Fiumara, J. Jankovic, M. Zappia (Catania, Italy)

Rare Genetic and Metabolic Diseases · Les Muses Terrace, Level 3

1:45pm-3:15pm: Hypophosphatasia presenting as parkinsonism with compound heterozygous mutations in ALPL gene

WF. Yu, ZX. Zhao, LW. Liu, JL. Hu, FF. Wang, YM. Liu (Jinan, China)

Rare Genetic and Metabolic Diseases · Les Muses Terrace, Level 3