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

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Articles tagged "Peripheral neuropathy"

  • 2017 International Congress

    Parkinson Disease-Associated Polyneuropathy: A Biomarker of Disease Severity?

    M. Rosso, A. Merola, A. Romagnolo, C. Comi, A. Fasano, M. Zibetti, R. Lopez-Castellanos, D. Cocito, L. Lopiano, A. Espay (Cincinnati, OH, USA)

    Objective: Objective: We sought to examine the association between Parkinson disease (PD) associated polyneuropathy (PD-PNP) and levodopa dose, age, and disease duration in a cross-sectional,…
  • 2017 International Congress

    Parkinson ‘ s disease and Peripheral Nervous System  : Wax and Waning Non-motor offs and Levodopa-use Topics

    s.g. echebarria mendieta (-, Spain)

    Objective: To relate the non-motor offs theory , sensory signs and levodopa use with neurophysiiology  terms in PD Background: Peripheral Nervous System disease concept in…
  • 2017 International Congress

    An unusual case of sporadic Creutzfeld Jacob disease presenting as acute neuropathy

    R. Hanumanthu, A. Alchaki, A. Nyaboga, H. Ghuman, J. Chen, E. Feinstein (Newark, NJ, USA)

    Objective: To describe an unusual case of sporadic Creutzfeld Jacob Disease (CJD) that initially presented with ascending tingling of lower extremities. Background: Prion diseases are…
  • 2017 International Congress

    Serum vitamin B12 levels in patients with Parkinson’s disease and its association with peripheral neuropathy and cognition

    R. Kandadai, N. Mathukumali, S.S. Meka, S. Tandra, A. Kohat, M. Kanikannan, R. Borgohain (Hyd, India)

    Objective: To compare serum Vitamin B12 levels among PD patients and normal controls and to assess the association of Vitamin B12 levels with various disease parameters, peripheral…
  • 2016 International Congress

    Ciprofloxacin as the cause of syndroma extrapiramidale

    D. Imamovic, N. Subasic, A. Nakicevic, E. Suljic (Sarajevo, Bosnia and Herzegowina)

    Objective: Ciprofloxacin in rare cases can cause paresthesia, dysesthesia, hypoesthesia, tremor, convulsions, dizziness . Background: The patient, 22 years old, comes in the emergency room,…
  • 2016 International Congress

    A peripheral pathway to restless legs syndrome? Clues from familial amyloid polyneuropathy

    T. Teodoro, P. Viana, D. Abreu, I. Conceição, R. Peralta, J.J. Ferreira (Lisboa, Portugal)

    Objective: To investigated if RLS is increased in familial amyloid polyneuropathy related to transthyretin (TTR-FAP) and to identify factors associated with RLS in this population.…
  • 2016 International Congress

    Prodromal criteria of spinocerebellar type 2: Lessons for physiopathology, natural history and therapeutical trials

    L. Velázquez-Pérez, R. Rodríguez-Labrada, N. Canales-Ochoa, J. Fernandez-Ruiz, J. Medrano-Montero, Y. Vazquez-Mojena, G. Auburger, U. Ziemann (Holguín, Cuba)

    Objective: To identify criteria defining the prodromal stage of spinocerebellar ataxia 2 (SCA2). Background: The prodromal stage of spinocerebellar ataxias has not been systematically studied…
  • 2016 International Congress

    Usefulness of total neuropathy score revised as a screening tool of peripheral neuropathy in patients with Parkinson’s disease

    P.W. Ko, J.S. Park, K. Kang, H.W. Lee (Daegu, Korea)

    Objective: To evaluate (1) prevalence of peripheral neuropathy and (2) usefulness of known neuropathy scores in patients with Parkinson's disease (PD). Background: Peripheral neuropathy has…
  • 2016 International Congress

    Ninjurin 1 gene D110a single nucleotide polymorphism as a genetic marker for nerve damage leprosy patients from South India

    A. Sundaramoorthy, S. Keshavarao, A. Valsala Gopalakrishnan (Coimbatore, India)

    Objective: Analyze the Ninjurin 1 gene single nucleotide polymorphisms in leprosy patients from south India, and the role of the gene in the nerve damage.…
  • 2016 International Congress

    Human, fly and cellular models of riboflavin transporter neuronopathy

    A. Manole, A. Pandraud, M.M. Reilly, J.E.C. Jepson, H. Houlden (London, United Kingdom)

    Objective: A) To find the spectrum of defects in riboflavin transporter genes; B) To ascertain the in-vitro cellular effects of SLC52A2 mutations and riboflavin on…
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