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Autosomal recessive adult onset ataxia

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

2022

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Longitudinal assessment of autonomic dysfunction in early Parkinson's disease

Parkinsonism & related disorders, 2019-09, Vol.66, p.74-79

2019

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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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Automatic Identification and Classification of Freezing of Gait Episodes in Parkinson's Disease Patients

IEEE transactions on neural systems and rehabilitation engineering, 2014-05, Vol.22 (3), p.685-694

2014

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Long-term outcome of patients with neurological form of Wilson’s disease compliant to the de-coppering treatment

Journal of neurology, 2023-07, Vol.270 (7), p.3492-3498

2023

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Gait Characteristics during Dual-Task Walking in Elderly Subjects of Different Ages

Brain sciences, 2024-01, Vol.14 (2), p.148

2024

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Gait in drug naïve patients with de novo Parkinson's disease - altered but symmetric

Neurological research (New York), 2015-08, Vol.37 (8), p.712-716

2015

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Chemical management of levodopa-induced dyskinesia in Parkinson's disease patients

Expert opinion on pharmacotherapy, 2019-01, Vol.20 (2), p.219-230

2019

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Selection of gait parameters for differential diagnostics of patients with de novo Parkinson's disease

Neurological research (New York), 2017-10, Vol.39 (10), p.853-861

2017

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NBIA Syndromes: A Step Forward from the Previous Knowledge

Neurology India, 2021-09, Vol.69 (5), p.1380-1388

2021

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Impact of depression on gait variability in Parkinson’s disease

Clinical neurology and neurosurgery, 2021-01, Vol.200, p.106324-106324, Article 106324

2021

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White matter abnormalities in Parkinson's disease patients with glucocerebrosidase gene mutations

Movement disorders, 2013-06, Vol.28 (6), p.772-778

2013

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Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism

Neurological research (New York), 2021-04, Vol.43 (4), p.321-326

2021

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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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Longitudinal brain connectivity changes and clinical evolution in Parkinson's disease

Molecular psychiatry, 2021-09, Vol.26 (9), p.5429-5440

2021

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The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy

Movement disorders, 2022-06, Vol.37 (6), p.1131-1148

2022

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C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population

Genetika (Beograd), 2022, Vol.54 (3), p.1313-1330

2022

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Dynamics of impulsive–compulsive behaviors in early Parkinson’s disease: a prospective study

Journal of neurology, 2020-04, Vol.267 (4), p.1127-1136

2020

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Gait alterations in Parkinson’s disease at the stage of hemiparkinsonism—A longitudinal study

PloS one, 2022-07, Vol.17 (7), p.e0269886-e0269886

2022

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Psychiatric Symptoms in the Initial Motor Stage of Parkinson's Disease

The journal of neuropsychiatry and clinical neurosciences, 2016, Vol.28 (3), p.205-210

2016

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Reply to: “Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism”

Movement disorders, 2023-04, Vol.38 (4), p.712-713

2023

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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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Mild Cognitive Impairment in Early Parkinson's Disease Using the Movement Disorder Society Task Force Criteria: Cross-Sectional Study in Hoehn and Yahr Stage 1

Dementia and geriatric cognitive disorders, 2015-01, Vol.40 (3-4), p.199

2015

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Cognitive impairment in multiple system atrophy: A position statement by the neuropsychology task force of the MDS multiple system atrophy (MODIMSA) study group

Movement disorders, 2014-06, Vol.29 (7), p.857-867

2014

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ANO10‐Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series

Movement disorders, 2024-05, Vol.39 (5), p.887-892

2024

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Autosomal recessive adult onset ataxia

Longitudinal assessment of autonomic dysfunction in early Parkinson's disease

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

Automatic Identification and Classification of Freezing of Gait Episodes in Parkinson's Disease Patients

Long-term outcome of patients with neurological form of Wilson’s disease compliant to the de-coppering treatment

Gait Characteristics during Dual-Task Walking in Elderly Subjects of Different Ages

Gait in drug naïve patients with de novo Parkinson's disease - altered but symmetric

Chemical management of levodopa-induced dyskinesia in Parkinson's disease patients

Selection of gait parameters for differential diagnostics of patients with de novo Parkinson's disease

NBIA Syndromes: A Step Forward from the Previous Knowledge

Impact of depression on gait variability in Parkinson’s disease

White matter abnormalities in Parkinson's disease patients with glucocerebrosidase gene mutations

Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism

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

Longitudinal brain connectivity changes and clinical evolution in Parkinson's disease

The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy

C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population

Dynamics of impulsive–compulsive behaviors in early Parkinson’s disease: a prospective study

Gait alterations in Parkinson’s disease at the stage of hemiparkinsonism—A longitudinal study

Psychiatric Symptoms in the Initial Motor Stage of Parkinson's Disease

Reply to: “Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism”

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

Mild Cognitive Impairment in Early Parkinson's Disease Using the Movement Disorder Society Task Force Criteria: Cross-Sectional Study in Hoehn and Yahr Stage 1

Cognitive impairment in multiple system atrophy: A position statement by the neuropsychology task force of the MDS multiple system atrophy (MODIMSA) study group

ANO10‐Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series

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