MDS Abstracts

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

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  • 2016 International Congress

    Orthostatic tremor: Is deep brain stimulation better than spinal cord stimulation?

    H.L. Chiang, Y. Tai, V.S.C. Fung, N. Mahant (Sydney, Australia)

    Objective: To describe 2 patients with orthostatic tremor (OT) who responded to deep brain stimulation (DBS). Background: OT is a rare movement disorder, characterized by…
  • 2016 International Congress

    Increase L-dopa dosage for rest tremor or think about the essential tremor too?

    A. Voskanyan, G. Avagyan, E. Khachatryan, K. Harutyunyan, S. Khachaturyan, H. Amirjanyan, H. Manvelyan (Yerevan, Armenia)

    Objective: A 57-year old man with hand tremor is diagnosed with Parkinson's disease (PD) and treated with high dose levodopa (L-dopa) during last 5 years,…
  • 2016 International Congress

    Towards a responsive deep brain stimulation for the treatment of essential tremor

    E. Opri, J. Shute, R. Molina, M. Okun, A. Gunduz, K. Foote (Gainesville, FL, USA)

    Objective: To identify neurophysiologic markers of intention tremor in the ventral intermediate thalamic nucleus (Vim) and hand motor cortex to develop closed-loop deep brain stimulation…
  • 2016 International Congress

    The scale for assessment and rating of ataxia in early onset ataxia; always a reliable biomarker?

    R. Brandsma, T.F. Lawerman, M.J. Kuiper, I.J. Lunsing, H. Burger, D.A. Sival (Groningen, Netherlands)

    Objective: To determine the reliability and discriminant validity of the Scale for Assessment and Rating of Ataxia (SARA) in early onset ataxia. Background: Early onset…
  • 2016 International Congress

    Depression and clinical progression in spinocerebellar ataxias

    S.H. Kuo, R.Y. Lo, K.P. Figueroa, S.M. Pulst, S. Perlman, G. Wilmot, C. Gomez, J. Schmahmann, H. Paulson, V.G. Shakkottai, S. Ying, T. Zesiewicz, K. Bushara, M. Geschwind, G. Xia, T. Ashizawa, S.H. Subramony (New York, NY, USA)

    Objective: To study the prevalence and influence of depressive symptoms in spinocerebellar ataxias (SCAs). Background: Depression is a common comorbidity in SCAs but its association…
  • 2016 International Congress

    Clinico-genetic correlation in Indian spinocerebellar ataxia (SCA1) patients

    A. Takkar, I. Ahmed, S. Shakya, V. Suroliya, R. Singh, A. Sonkar, A.K. Srivastava, M. Faruq (New Delhi, India)

    Objective: To report the Clinico-genetic correlation in Spinocerebellar ataxia type 1 (SCA1) Patients in Indian Population. Background: Spinocerebellar ataxia type 1(SCA1) is a neurodegenerative disease…
  • 2016 International Congress

    Hereditary spastic paraplegia caused by heterozygous AFG3L2 and SPG7 mutations

    C.D. Stephen, J.D. Schmahmann (Boston, MA, USA)

    Objective: To report a new late-onset autosomal recessive spastic paraplegia caused by heterozygous mutations in the AFG3L2 and SPG7 genes. Background: The hereditary spastic paraplegias…
  • 2016 International Congress

    Persistent hemichorea and caudate atrophy in untreated diabetic striatopathy

    B. Krishnaiah, E. Lucassen, M.C. Stahl (Hershey, PA, USA)

    Objective: To describe the natural history and imaging findings in a case of untreated diabetic striatopathy. Background: Diabetic striatopathy (DS) is a rare movement disorder…
  • 2016 International Congress

    Dysphagia in early stage Huntington’s disease (HD) – Pilot observations from a multimodal imaging study

    I. Trender-Gerhard, E. Michou, A. Gerhard, D. Craufurd, S. Hamdy, K. Herholz (Manchester, United Kingdom)

    Objective: To assess the central neural control of swallowing in HD patients with mild dysphagia using a multimodal imaging approach combining qualitative and quantitative swallowing…
  • 2016 International Congress

    Temporal course of the total motor score in Huntington disease

    P. Auinger, T.J. Felong, S. Gandhi, V. Abler, K. Biglan, S. Papapetropoulos, C. Venuto, R. Dorsey (Rochester, NY, USA)

    Objective: To describe the temporal course of motor features in Huntington disease (HD) using the Unified Huntington Disease Rating Scale - Total Motor Score (UHDRS-TMS)…
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