MDS Abstracts

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

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2025 International Congress » MSA, PSP, CBS (Other)

Meeting: 2025 International Congress

Atypical Parkinsonian Syndromes Presenting with Homonymous Hemianopsia

T. Le, D. Truong, M. Aung (Houston, USA)

Atypical Parkinsonism with LRRK2 Mutation Presenting as Multiple System Atrophy

K. Makhoul, R. Ramdhani (Great neck, USA)

Clinical Deficits, Quality of Life and Caregiver Burden across PSP Phenotypes

A. Cámara, I. Zaro, C. Painous, Y. Compta (Barcelona, Spain)

Clinical Features Suggestive of Alpha-Synucleinopathy in Progressive Supranuclear Palsy

C. Painous, A. Martínez-Reyes, J. Santamaria, M. Fernández, A. Cámara, Y. Compta (Barcelona, Spain)

Conjugal Parkinsonism

CK. Tan (Singapore, Singapore)

Description possible enviromental exposure in AMS Latin America population

M. Cesarini, N. Gonzalez Rojas, M. Espindola, G. da Prat, JL. Etcheverry, E. Gatto (Buenos Aires, Argentina)

Dopa-Responsive Parkinsonism Secondary to Tauopathy: Clinical, Pathological, and Genetic Study

S. Giri Ravindran, B. Daud Shah, E. Noyes, V. Zherebitskiy, A. Rajput, M. Farrer, A. Rajput (Saskatoon, Canada)

Expanding the Spectrum of Alzheimer’s Disease Clinical Presentations: Progressive Dysarthria with Monomelic Tremor

O. Carranza-Renteria, G. Gliebus (Boca Raton, USA)

Exploring Cardiac Autonomic Dysfunction in Synucleinopathies with Parkinsonism Across Awake-Sleep Stages

N. Limotai, T. Somboon, S. Rujirussawarawong, T. Tumnark, N. Suanprasert, N. Unwanatham, C. Limotai (Bangkok, Thailand)

Identification of Genetic Variants in Progressive Supranuclear Palsy in China

Y. Kang, W. Luo (Hangzhou, China)

Normal Pressure Hydrocephalus in Vestibular Schwannoma Patients

T. Davidy, S. Anis, T. Goldberg, A. Fay-Karmon, Y. Zauberman, N. Rennert, O. Lesman-Segev, S. Hassin-Baer (Cleveland, USA)

Pathogenic TBK1 Mutation Associated with Multiple System Atrophy-Like Phenotype

S. Barton, C. Siskind, H. Zahed (Palo Alto, USA)

Unraveling the Genetic Architecture of Progressive Supranuclear Palsy in East Asians

P. Chen, R. Lin, N. Lee, J. Hsu, C. Tai, R. Wu, H. Chiang, Y. Wu, C. Lu, H. Chang, T. Lee, Y. Chang, C. Lin (Taipei, Taiwan)

Unveiling a rare case: Novel TBK1 variant presenting as Multiple system atrophy-like phenotype

R. Kandadai, M. Karri, S. Kola, R. Borgohain, R. Alugolu, P. Vvsrk, A. Nalamasa (Hyderabad, India)

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