Search Results - "DRAGASEVIC, Natasa"

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  1. 1

    Gait alterations in Parkinson’s disease at the stage of hemiparkinsonism—A longitudinal study by Markovic, Vladana, Stankovic, Iva, Radovanovic, Sasa, Petrovic, Igor, Jecmenica Lukic, Milica, Dragasevic Miskovic, Natasa, Svetel, Marina, Kostic, Vladimir

    Published in PloS one (21-07-2022)
    “…Background Progressive gait impairment in Parkinson’s disease (PD) leads to significant disability. Quantitative gait parameters analysis provides valuable…”
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    Journal Article
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    Autosomal recessive adult onset ataxia by Dragašević-Mišković, Nataša, Stanković, Iva, Milovanović, Andona, Kostić, Vladimir S.

    Published in Journal of neurology (2022)
    “…Autosomal recessive ataxias (ARCA) represent a complex group of diseases ranging from primary ataxias to rare and complex metabolic disorders in which ataxia…”
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    Journal Article
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    Impact of depression on gait variability in Parkinson’s disease by Dragašević-Mišković, Nataša T, Bobić, Vladislava, Kostić, Milutin, Stanković, Iva, Radovanović, Saša, Dimitrijević, Kosta, Svetel, Marina, Petrović, Igor, Đurić-Jovičić, Milica

    Published in Clinical neurology and neurosurgery (01-01-2021)
    “…•Depression is associated with gait variability especially in a dual-task condition.•Swing time variability might be particularly sensitive to an impact of…”
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    Analysis of on-surface and in-air movement in handwriting of subjects with Parkinson's disease and atypical parkinsonism by Miler Jerkovic, Vera, Kojic, Vladimir, Dragasevic Miskovic, Natasa, Djukic, Tijana, Kostic, Vladimir S, Popovic, Mirjana B

    Published in Biomedizinische Technik (24-04-2019)
    “…The purpose of this paper is to emphasize the importance of in-air movement besides on-surface movement for handwriting analysis. The proposed method uses a…”
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    Is there a specific psychiatric background or personality profile in functional dystonia? by Tomić, Aleksandra, Petrović, Igor, Pešić, Danilo, Vončina, Marija Mitković, Svetel, Marina, Mišković, Nataša Dragašević, Potrebić, Aleksandra, Toševski, Dušica Lečić, Kostić, Vladimir S

    Published in Journal of psychosomatic research (01-06-2017)
    “…Abstract Objective The aim of this cross-sectional study was to identify if there was a specific difference between patients with functional dystonia (DysF)…”
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    Finger tapping analysis in patients with Parkinson’s disease and atypical parkinsonism by Djuric-Jovicica, Milica, Petrovicb, Igor, Jecmenica-Lukicb, Milica, Radovanovicc, Sasa, Dragasevic-Miskovicb, Natasa, Belica, Minja, Miler-Jerkovicd, Vera, Popovicd, Mirjana B, Kosticb, Vladimir S

    Published in Journal of clinical neuroscience (01-08-2016)
    “…Highlights • Finger tapping performance (FTP) was objectively recorded in Parkinson’s disease (PD) patients. • FTP was also recorded in progressive…”
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    Changes of Phenotypic Pattern in Functional Movement Disorders: A Prospective Cohort Study by Tomić, Aleksandra, Ječmenica Lukić, Milica, Petrović, Igor, Svetel, Marina, Dragašević Mišković, Nataša, Kresojević, Nikola, Marković, Vladana, Kostić, Vladimir S

    Published in Frontiers in neurology (05-11-2020)
    “…Functional movement disorders (FMD) refer to a group of movement disorders that present with clinical characteristics incongruent to those due to established…”
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  10. 10

    Motor imagery ability in patients with functional dystonia by Tomić, Aleksandra, Ječmenica Lukić, Milica, Petrović, Igor, Korkut, Vladimir, Kresojević, Nikola, Marković, Vladana, Dragašević Mišković, Nataša, Svetel, Marina, Kostić, Vladimir S.

    Published in Journal of psychosomatic research (01-12-2024)
    “…Motor imagery (MI) involves recreating a movement mentally without physically performing the movement itself. MI has a positive impact on motor performance,…”
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    Wilson’s disease by Svetel, Marina, Kresojevic, Nikola, Tomic, Aleksandra, Jecmenica-Lukic, Milica, Markovic, Vladana, Stankovic, Iva, Petrovic, Igor, Pekmezovic, Tatjana, Novakovic, Ivana, Bozic, Marija, Svetel, Marko, Vitkovic, Jelena, Dragasevic, Natasa

    Published in Srpski arhiv za celokupno lekarstvo (01-01-2024)
    “…Wilson?s disease (WD) is an autosomal recessive inherited disorder of copper metabolism caused by mutations in the ATP7B gene, which is located on chromosome…”
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    C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population by Marjanovic, Ana, Dobricic, Valerija, Jecmenica-Lukic, Milica, Stankovic, Iva, Milicevic, Ognjen, Dragasevic-Miskovic, Natasa, Brankovic, Marija, Jankovic, Milena, Novakovic, Ivana, Svetel, Marina, Stefanova, Elka, Kostic, Vladimir

    Published in Genetika (Beograd) (2022)
    “…These include, among others, two forms of atypical Parkinsonism, multiple system atrophy (MSA) and progressive supranuclear palsy (PSP). This study aimed to…”
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    Factors associated with deterioration of health-related quality of life in multiple system atrophy: 1-year follow-up study by Jecmenica-Lukic, Milica V., Pekmezovic, Tatjana D., Petrovic, Igor N., Dragasevic, Natasa T., Kostić, Vladimir S.

    Published in Acta neurologica Belgica (01-12-2018)
    “…The aim of this study was to identify the main contributors to the health-related quality of life (HRQoL) in multiple system atrophy with predominant…”
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    Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism by Pešić, Milica, Dragašević Mišković, Nataša, Marjanović, Ana, Dobričić, Valerija, Maksimović, Nela, Svetel, Marina, Perović, Dijana, Novaković, Ivana, Cirković, Sanja, Stanković, Iva, Kostić, Vladimir

    Published in Neurological research (New York) (03-04-2021)
    “…Introduction: Although one of the most common monogenic late-onset neurodegenerative disorders, fragile-X-associated tremor/ataxia syndrome (FXTAS) is still…”
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    Dystonia in Patients With Spinocerebellar Ataxia Type 2 by Markovic, Vladana, Dragasevic‐Miskovic, Natasa T., Stankovic, Iva, Petrovic, Igor, Svetel, Marina, Kostić, Vladimir S.

    “…Dystonia has been described in various genetically proven spinocerebellar ataxias (SCAs), most often in SCA3, SCA17, and SCA2 patients. In this report, we…”
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    Therapeutic efficacy of bilateral prefrontal slow repetitive transcranial magnetic stimulation in depressed patients with Parkinson's disease: An open study by Dragaševic, Nataša, Potrebić, Aleksandra, Damjanović, Aleksandar, Stefanova, Elka, Kostić, Vladimir S.

    Published in Movement disorders (01-05-2002)
    “…Recent studies have suggested that both high‐ and low‐frequency repetitive transcranial magnetic stimulation (rTMS) have antidepressant effects in patients…”
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    Pattern of disease progression in atypical form of pantothenate-kinase-associated neurodegeneration (PKAN) – Prospective study by Tomić, Aleksandra, Petrović, Igor, Svetel, Marina, Dobričić, Valerija, Dragašević Mišković, Nataša, Kostić, Vladimir S

    Published in Parkinsonism & related disorders (01-05-2015)
    “…Abstract Introduction Classic form of pantothenate-kinase-associated neurodegeneration (PKAN), caused by mutation in PANK2 gene, is characterized by early…”
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