MDS Abstracts

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

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  • 2017 International Congress

    Prevalence of tremor in Multiple Sclerosis in Isfahan, Iran

    M. Salari, M. Etemadifar, O. Mirmosayyeb (Isfahan, Islamic Republic of Iran)

    Objective: To evaluate prevalence of tremor in Multiple sclerosis in Isfahan Background: Multiple sclerosis (MS) is demyelinating disease of central nervous system (CNS), affecting mostly…
  • 2017 International Congress

    Head tremor in supine position does not differentiate essential tremor and cervical dystonia

    E. Ruzicka, R. Krupicka, T. Duspivova, O. Ulmanova, P. Holly, V. Cejka, J. Rusz, R. Jech (Praha, Czech Republic)

    Objective: Using objective instrumental methods, we aimed to verify the clinical utility of sitting/supine test and other clinical features to differentiate between ET and DT.…
  • 2017 International Congress

    Audiological Evaluation in Sporadic Ataxia

    B. Zeigelboim, H. Teive, A. Scheidt, K. Kronbauer, J. Faryniuk, T. Oliveira, F. Fernandes (Curitiba, Brazil)

    Objective: to describe the audiological and electrophysiological results  in patients with sporadic ataxia (SA). Background: Patients with adult onset non-familial progressive ataxia are classified in…
  • 2017 International Congress

    The autonomic nervous system in Friedreich´s Ataxia: preliminary findings

    E. Indelicato, A. Fanciulli, J. Wanschitz, W. Nachbauer, W. Poewe, G. Wenning, S. Boesch (Innsbruck, Austria)

    Objective: To investigate the autonomic function in Friedreich´s ataxia (FRDA)   Background: FRDA is a hereditary neurodegenerative disorder characterized by progressive gait ataxia, limb dysmetria, dysarthria…
  • 2017 International Congress

    Autosomal Dominant Spinocerebellar Ataxia Secondary to CACNA1G in a Patient of German Ancestry

    E. Call, V. Santini (Stanford, CA, USA)

    Objective: We describe the case of a male patient of German ancestry with SCA 42. Background: Hereditary spinocerebellar ataxia (SCA) describes a heterogeneous group of…
  • 2017 International Congress

    New XK deletion associated with McLeod syndrome

    A. DoedeMaindreville, G. Jouret, E. Landais, P. Feucher, S. Bakchine, D. Gaillard, A.S. Lebre (Reims, France)

    Objective: To describe a new XK deletion associated with McLeod syndrome. Background: McLeod syndrome is a rare genetic syndrome characterized by the association of chorea…
  • 2017 International Congress

    White matter lesions and peripheral vessel reactivity in dementia with Lewy bodies

    A. Chimagomedova, E. Vasenina, O. Levin (Moscow, Russian Federation)

    Objective: We aimed to assess the significance of white matter hyperintensities (WMHs) in dementia with Lewy bodies (DLB) and their contribution to phenotype of the…
  • 2017 International Congress

    Cefepime-induced encephalopathy and myoclonus

    T. Rasameesoraj, X.x. Yu, A. Ahmed, H. Fernandez (Cleveland, OH, USA)

    Objective: To raise awareness of cephalosporin-induced encephalopathy and myoclonus. Background: Myoclonus occurs in 15% of antibiotic-associated encephalopathy, especially with penicillins and cephalosporins. Cefepime and ceftazidime…
  • 2017 International Congress

    MRI-based Brain Networks of Perfusion and Structural Abnormalities in Patients with Cerebellar Variant of Multiple System Atrophy

    P. Wu, S. Peng, J. Ge, J. Wang, D. Eidelberg, C. Zuo, Y. Ma (Shanghai, China)

    Objective: To identify MRI-based brain networks of cerebral perfusion and structural abnormalities in cerebellar variant of MSA.  Background: MSA consists clinically of parkinsonian (MSA-P) and cerebellar (MSA-C) variants. Previous FDG PET studies have…
  • 2017 International Congress

    Striatal dopamine transporter abnormalities in pure autonomic failure and speculation about the relationship with Lewy bodies

    M. Yogo, M. Morita, M. Suzuki (Tokyo, Japan)

    Objective: To reveal dopamine transporter (DAT) abnormalities in pure autonomic failure (PAF) and speculate about the relationship with the Lewy body progression pathway.    Background:…
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