2018 International Congress Archives - Page 34 of 177

Classifying carriers of the G2019S mutation in the LRRK2 gene using MRI radiomics analysis

M. Artzi, A. Thaler, A. Orr Urterger, T. Hendler, M. Sela, A. Mirelman, D. Ben Bashat (Tel Aviv, Israel)
Classifying Parkinsonian Gait and Turning in Daily Life with Wearable Technology

F. Horak, J. McNames, M. El Gohary, J. Nutt, C. Curtze (Portland, OR, USA)
Clinical and functional network features of visuoperceptual disturbances in Parkinson’s disease

K. Kawabata, H. Watanabe, R. Ohdake, K. Hara, E. Bagarinao, T. Kato, A. Ogura, M. Masuda, T. Yokoi, T. Tsuboi, M. Katsuno, G. Sobue (Nagoya, Japan)
Clinical and genetic data of Huntington disease in Uzbekistan patient

M. Rakhimova (Tashkent, Uzbekistan)
Clinical and genetic heterogeneity in portuguese patients with Hereditary Spastic Paraplegia

I. Cunha, A. Brás, J. Ribeiro, C. Januário (Coimbra, Portugal)
Clinical and genetics characterization of patients with Myoclonus Dystonia Syndrome

B. Perez-Dueñas, M. Vanegas, L. Marti, A. Darling, D. Ortigoza-Escobar, S. Candela, H. Baide, J. Campistol, S. Aguilera, M. Marti, A. Macaya (Barcelona, Spain)
Clinical and imaging progression in the PARS cohort: Results from 6 years of observation

D. Jennings, A. Siderowf, S. Eberly, D. Oakes, M. Stern, K. Marek (New Haven, CT, USA)
Clinical and Molecular Characterization of a Family with Ataxia with Oculomotor Apraxia Type 2

T. Tropea, N. Jain, T. Unger, A. Chen-Plotkin. (Philadelphia, PA, USA)
Clinical and morphometric features of the tics

S. Munasipova, Z. Zalyalova (Kazan, Russian Federation)
Clinical and mutation spectrum of Ataxia with oculomotor apraxia-2: An Indian perspective

S. Shakya, M. Faruq, A. Srivastava, I. Singh, A. Garg, R. Rajan, V. Goyal (New Delhi, India)