2016 International Congress

Tuesday, June 21, 2016

12:30pm-2:00pm

Eye movement abnormalities in essential tremor and other neurodegenerative diseases (Parkinson’s disease, spino-cerebellar ataxia, Huntington disease)

M. Wojcik-Pedziwiatr, M. Rudzinska, K. Zajdel, W. Soltan, J. Slawek, A. Szczudlik (Krakow, Poland)

Tremor  ·  Exhibit Hall located in Hall B, Level 2

12:30pm-2:00pm

F1 crossbreds of C57BL/6 and CD-1 mice demonstrate resistance to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) induced nigral neurodegeneration

P.A. Alladi, D. Vidyadhara, H. Yarreiphang, T.R. Raju (Bengaluru, India)

Parkinson's disease: Pathophysiology  ·  Exhibit Hall located in Hall B, Level 2

12:30pm-2:00pm

Fahr’s syndrome in a Filipino female with hearing loss and polycystic ovaries: A case report

P.D. Dadgardoust, R.L. Rosales (Manila, Philippines)

Myoclonus  ·  Exhibit Hall located in Hall B, Level 2

12:30pm-2:00pm

Faithful SGCE imprinting in iPSC-derived cortical neurons: An endogenous model system of myoclonus-dystonia

K. Grütz, P. Seibler, A. Weißbach, K. Lohmann, F.A. Carlisle, D.J. Blake, A. Westenberger, C. Klein, A. Grünewald (Lübeck, Germany)

Pathophysiology (other movement disorders)  ·  Exhibit Hall located in Hall B, Level 2

12:30pm-2:00pm

Falls in Parkinson’s disease: Beware the short, slow steps

A. Lieberman, A. Deep, S. Shafer, T. Lockhart (Phoenix, AZ, USA)

Parkinson's disease: Pathophysiology  ·  Exhibit Hall located in Hall B, Level 2

12:30pm-2:00pm

Familial Parkinson’s disease in Ireland

D.A. Olszewska, A. McCarthy, B. Magennis, O. Ross, T. Lynch (Dublin, Ireland)

Parkinson's disease: Genetics  ·  Exhibit Hall located in Hall B, Level 2

12:30pm-2:00pm

Familial Parkinson’s disease in the Province of Quebec

L.L. Farrell, E. Pourcher, E. Nosova, M. McKenzie, I. Guella, D.M. Evans, C. Déry, M.J. Farrer (Vancouver, BC, Canada)

Parkinson's disease: Genetics  ·  Exhibit Hall located in Hall B, Level 2

12:30pm-2:00pm

Familial SPG17/distal hereditary motor neuropathy type V– Complicated hereditary spastic paraplegia with many faces

T. Musacchio, A.K. Zaum, N. Üceyler, C. Sommer, N. Pfeifroth, K. Reiners, E. Kunstmann, J. Volkmann, S. Rost, S. Klebe (Würzburg, Germany)

Genetics (NON-PD)  ·  Exhibit Hall located in Hall B, Level 2

12:30pm-2:00pm

FBOX07 mutation with juvenile parkinsonism and behavioral disorders

M. Kuzu, F.N. Durmaz, Ç. Ulukan, H. Kaymakçalan, A.O. Çaglayan, C. Akbostanci (Ankara, Turkey)

Parkinson's disease: Genetics  ·  Exhibit Hall located in Hall B, Level 2

12:30pm-2:00pm

Floor square size predicts step count of 360° turns in PD patients with freezing

U.M. Fietzek, L. Stuhlinger, A. Plate, A.O. Ceballos-Baumann, K. Bötzel (Munich, Germany)

Parkinson's disease: Pathophysiology  ·  Exhibit Hall located in Hall B, Level 2