MDS Abstracts

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

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Articles tagged "Dystonia: Clinical features"

  • 2019 International Congress

    Geste antagoniste in Catalan art – Santiago Rusiñol’s Laughing Girl

    F. Germiniani, P. Marques, L. Pinheiro, G. Franklin, G. Ribas, H. Teive (Curitiba, Brazil)

    Objective: Our aim is to analyze how the Catalan picture  Laughing Girl (La Risueña)could be a depiction of geste antagoniste. Background: Santiago Rusiñol was a…
  • 2019 International Congress

    Oromandibular Dystonia: Clinical Data from 68 Patients

    M. Balal, M. Demirkiran (Adana, Turkey)

    Objective: To determine the demographic and clinical data of patients with oromandibular dystonia (OMD). Background: Dystonia is a type of movement disorder characterized by sustained,…
  • 2019 International Congress

    Genotype-phenotype relations for the isolated Dystonia Genes TOR1A, THAP1, GNAL, ANO3, KMT2B, PRKRA and HPCA: MDSGene Systematic Review

    LM. Lange, J. Junker, S. Loens, L. Olschewski, S. Schaake, S. Petkovic, M. Kasten, A. Westenberger, A. Domingo, A. Madoev, I. König, C. Marras, KP. Bhatia, S. Camargos, C. Klein, K. Lohmann (Lübeck, Germany)

    Objective: To systematically review genotypes and phenotypes of monogenic isolated dystonia. Background: The Movement Disorder Society Genetic mutation database (MDSGene at www.mdsgene.org) provides an overview…
  • 2019 International Congress

    Pregnancy and Delivery Complications in Women with Inherited Isolated Dystonia

    M. San Luciano, V. Shanker, S. Bressman, D. Raymond, R. Saunders-Pullman (San Francisco, CA, USA)

    Objective: To determine whether female mutation carriers of inherited dopa-responsive (DRD) and DYT/TOR1A genes had higher pregnancy and delivery complications than non-carriers Background: Women with…
  • 2019 International Congress

    Neurology Residents Versus a Mobile Medical Application in deducing differential diagnoses in Movement Disorders: A multi-center, cross-sectional, observational study

    V. Vishnu, P. Vinny, R. Rajan, V. Goyal, P. Srivastava, V. Lal, P. Sylaja, L. Narasimhan, S. Dwivedi, P. Nair, D. Ramachandran, A. Gupta (New Delhi, India)

    Objective: To test the hypothesis that the differentials generated by the  Mobile Medical Application  are more clinically relevant and complete to the ones derived by…
  • 2019 International Congress

    Stimulus-induced paroxysmal cranial dyskinesia and Nail Patella Syndrome in a multigenerational family with a novel mutation in the LMX1B gene

    S. Bech, A. Loekkegaard, T. Nielsen, A. Nørremølle, L. Hasholt, Y. Mang, J. Nielsen, H. Eiberg, L. Hjermind (Copenhagen, Denmark)

    Objective: To perform a genetic linkage study with the aim to identify the cause of dyskinesia in a large family with affected members in several…
  • 2019 International Congress

    Combined Botulinum Toxin and Gpi DBS therapy in intractable cervical dystonia

    AM. Macerollo, BH. Hammersley, ME. Esposito, JS. Somerset, RE. Ellis, MB. Bonello, JP. Panicker, DD. Damodoran, JOF. Farah, PE. Eldridge, SA. Alusi (Naples, Italy)

    Objective: To test whether the reintroduction of Botulinum Toxin Injections (BTI) after Globus pallidus interna Deep Brain Stimulation (Gpi-DBS) for intractable cervical dystonia synergistically improves…
  • 2019 International Congress

    Cerebellar brain inhibition and cervical dystonia: exploring clinico-electrophysiological associations

    R. Sondergaard, LS. Gan, Y. Jasaui, J. Sarna, S. Furtado, T. Pringsheim, D. Martino (Calgary, AB, Canada)

    Objective: To examine the association between clinical features of cervical dystonia (CD) and cerebellar inhibition of the motor cortex (M1). Background: The involvement of cerebellar…
  • 2019 International Congress

    Pantothenate kinase-associated neurodegeneration in Tunisian families

    H. Benrhouma, I. Kraoua, H. Klaa, A. Rouissi, EM. Valente, I. Benyoussef Turki (Tunis, Tunisia)

    Objective: To describe clinical features, imaging and genetic findings of 6 Tunisian families diagnosed with PKAN. Background: Pantothenate kinase-associated neurodegeneration (PKAN) is an autosomal recessive…
  • 2019 International Congress

    The impact of physical activity and exercise on people living with dystonia

    L. Bradnam, R. Meiring, A. Mccambridge (Auckland, New Zealand)

    Objective: The objective was to conduct a survey to elucidate the impact of exercise and physical activity on dystonia and identify barriers to participation. Background:…
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