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Clinical outcomes of two main variants of progressive supranuclear palsy and multiple system atrophy: a prospective natural history study

Journal of neurology, 2014-08, Vol.261 (8), p.1575-1583

2014

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Longitudinal clinical, cognitive, and neuroanatomical changes over 5 years in GBA-positive Parkinson’s disease patients

Journal of neurology, 2022-03, Vol.269 (3), p.1485-1500

2022

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Cognitive impairment and structural brain damage in multiple system atrophy-parkinsonian variant

Journal of neurology, 2020, Vol.267 (1), p.87-94

2020

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C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome

Journal of neurology, 2014-10, Vol.261 (10), p.1917-1921

2014

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Prevalence of non-motor symptoms in young-onset versus late-onset Parkinson’s disease

Journal of neurology, 2013-01, Vol.260 (1), p.131-137

2013

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Functional MRI connectivity of the primary motor cortex in functional dystonia patients

Journal of neurology, 2022-06, Vol.269 (6), p.2961-2971

2022

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DYT-THAP1: exploring gene expression in fibroblasts for potential biomarker discovery

Neurogenetics, 2024-04, Vol.25 (2), p.141-147

2024

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Structural brain heterogeneity underlying symptomatic and asymptomatic genetic dystonia: a multimodal MRI study

Journal of neurology, 2024-04, Vol.271 (4), p.1767-1775

2024

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Autosomal recessive adult onset ataxia

Journal of neurology, 2022, Vol.269 (1), p.504-533

2022

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Glucocerebrosidase and parkinsonism: lessons to learn

Journal of neurology, 2016-05, Vol.263 (5), p.1033-1044

2016

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Clinical, cognitive, and behavioural correlates of white matter damage in progressive supranuclear palsy

Journal of neurology, 2014-05, Vol.261 (5), p.913-924

2014

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Spread of primary dystonia in relation to initially affected region

Journal of neurology, 2007-07, Vol.254 (7), p.879-883

2007

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Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory Center

Neurogenetics, 2024-07, Vol.25 (3), p.193-200

2024

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Brain Calcification and Movement Disorders

Current Neurology and Neuroscience Reports, 2017, Vol.17 (1), p.2-2, Article 2

2017

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Quality of life in patients with progressive supranuclear palsy: one-year follow-up

Journal of neurology, 2015-09, Vol.262 (9), p.2042-2048

2015

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Indoor and outdoor falls in persons with Parkinson’s disease after 1 year follow-up study: differences and consequences

Neurological sciences, 2016-04, Vol.37 (4), p.597-602

2016

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Incidence and prediction of falls in Parkinson's disease: a prospective cohort study

European journal of epidemiology, 2015-04, Vol.30 (4), p.349-352

2015

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Clinical course of patients with pantothenate kinase-associated neurodegeneration (PKAN) before and after DBS surgery

Journal of neurology, 2019-12, Vol.266 (12), p.2962-2969

2019

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Characteristics of two distinct clinical phenotypes of functional (psychogenic) dystonia: follow-up study

Journal of neurology, 2018-01, Vol.265 (1), p.82-88

2018

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Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience

Journal of neurology, 2022-06, Vol.269 (6), p.3167-3174

2022

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A laboratory-based study on patients with Parkinson's disease and seborrheic dermatitis: the presence and density of Malassezia yeasts, their different species and enzymes production

BMC dermatology, 2014-03, Vol.14 (1), p.5-5, Article 5

2014

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Transcranial midbrain sonography and depressive symptoms in patients with Parkinson’s disease

Journal of neurology, 2015-03, Vol.262 (3), p.689-695

2015

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Prevalence of restless legs syndrome among adult population in a Serbian district: a community-based study

European journal of epidemiology, 2013-11, Vol.28 (11), p.927-930

2013

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Quality of life in patients with primary restless leg syndrome: community-based study

Neurological sciences, 2015-08, Vol.36 (8), p.1345-1351

2015

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Validation and cross-cultural adaptation of the Self-Assessment Disability Scale in patients with Parkinson’s disease in Serbia

Journal of neurology, 2013-08, Vol.260 (8), p.1970-1977

2013

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Clinical outcomes of two main variants of progressive supranuclear palsy and multiple system atrophy: a prospective natural history study

Longitudinal clinical, cognitive, and neuroanatomical changes over 5 years in GBA-positive Parkinson’s disease patients

Cognitive impairment and structural brain damage in multiple system atrophy-parkinsonian variant

C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome

Prevalence of non-motor symptoms in young-onset versus late-onset Parkinson’s disease

Functional MRI connectivity of the primary motor cortex in functional dystonia patients

DYT-THAP1: exploring gene expression in fibroblasts for potential biomarker discovery

Structural brain heterogeneity underlying symptomatic and asymptomatic genetic dystonia: a multimodal MRI study

Autosomal recessive adult onset ataxia

Glucocerebrosidase and parkinsonism: lessons to learn

Clinical, cognitive, and behavioural correlates of white matter damage in progressive supranuclear palsy

Spread of primary dystonia in relation to initially affected region

Frequency of C9orf72, GRN, and MAPT pathogenic variants in patients recruited at the Belgrade Memory Center

Brain Calcification and Movement Disorders

Quality of life in patients with progressive supranuclear palsy: one-year follow-up

Indoor and outdoor falls in persons with Parkinson’s disease after 1 year follow-up study: differences and consequences

Incidence and prediction of falls in Parkinson's disease: a prospective cohort study

Clinical course of patients with pantothenate kinase-associated neurodegeneration (PKAN) before and after DBS surgery

Characteristics of two distinct clinical phenotypes of functional (psychogenic) dystonia: follow-up study

Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience

A laboratory-based study on patients with Parkinson's disease and seborrheic dermatitis: the presence and density of Malassezia yeasts, their different species and enzymes production

Transcranial midbrain sonography and depressive symptoms in patients with Parkinson’s disease

Prevalence of restless legs syndrome among adult population in a Serbian district: a community-based study

Quality of life in patients with primary restless leg syndrome: community-based study

Validation and cross-cultural adaptation of the Self-Assessment Disability Scale in patients with Parkinson’s disease in Serbia

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