2025 International Congress » Paroxysmal Movement Disorders

Meeting: 2025 International Congress

A case of bilateral asterixis following hemichorea-hemiballism due to bilateral internal carotid artery stenosis

S. Mamada, R. Yokoyama, K. Seo, H. Kawasaki, Y. Ito, G. Oyama, T. Yamamoto (Saitama, Japan)

A Clinical Overlap Presentation of Episodic Ataxia Type 2 and Periodic Paralysis with a Novel Mutation in CACNA1A

C. Vila, K. Minks, P. Morrison (Rochester, USA)

Development of Gene Panel by Next‐Generation Sequencing Approach for Diagnosis of Paroxysmal Movement Disorders

PS. Somanna, RS. Sampath, PLK. Kukkle, AK. Kolandaswamy, VKN. Nanjundagowda, RP. P, UR. R, KK. Kotha, PA. Agarwal, SNS. N S, AR. Raina, PKS. Kumar S, GM. Majigoudra (Bangalore, India)

Episodic Rocking Movements in a Young Boy.

A. Singh, J. Singhvi, D. Das, I. Goel (Mohali, India)

Novel CUX2 Mutation Identified in Patient with Clinical Paroxysmal Nonkinesigenic Dyskinesia

C. Cheung, G. Osaki Mark, K. Mackenzie (Elk Grove, USA)

Paroxysmal Nonkinesigenic Dyskinesia in GLUT1 Deficiency Syndrome: A Rare Manifestation

A. Medhus, E. Krause (Austin, USA)

Phenotypic Spectrum of Movement Disorders in TBC1D24 Gene Variants: A Case Series

K. Chesky, M. Parnes, M. Hull (Houston, USA)

Phenotypic Variability Across Four Generations in a Family with CACNA1A Mutation

R. Usman, M. Moreno Escobar (Morgantown, USA)

Study Of Epidemiological and Clinical Profile of Neurologic Wilson’s Disease from a Tertiary Care Hospital In India

A. Kumar, A. Ranjan, R. Solanke, J. Sharma, S. Kumar (Patna, India)

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