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The topography of brain damage at different stages of Parkinson's disease

Human brain mapping, 2013-11, Vol.34 (11), p.2798-2807

2013

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ATP13A2 variants in early-onset Parkinson's disease patients and controls

Movement disorders, 2009-10, Vol.24 (14), p.2104-2111

2009

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Mild cognitive impairment in Parkinson's disease is associated with a distributed pattern of brain white matter damage

Human brain mapping, 2014-05, Vol.35 (5), p.1921-1929

2014

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Quality of life in patients with focal dystonia

Clinical neurology and neurosurgery, 2009-02, Vol.111 (2), p.161-164

2009

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Gait characteristics in patients with major depression performing cognitive and motor tasks while walking

Psychiatry research, 2014-06, Vol.217 (1), p.39-46

2014

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Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation

Annals of neurology, 2006-02, Vol.59 (2), p.248-256

2006

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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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Safety and efficacy of perampanel in advanced Parkinson's disease: A randomized, placebo-controlled study

Movement disorders, 2010-05, Vol.25 (7), p.896-905

2010

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MRI measurements of brainstem structures in patients with Richardson's syndrome, progressive supranuclear palsy-parkinsonism, and Parkinson's disease

Movement disorders, 2011-02, Vol.26 (2), p.247-255

2011

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Bcl-2: Prolonging Life in a Transgenic Mouse Model of Familial Amyotrophic Lateral Sclerosis

Science (American Association for the Advancement of Science), 1997-07, Vol.277 (5325), p.559-562

1997

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Status dystonicus: Predictors of outcome and progression patterns of underlying disease

Movement disorders, 2012-05, Vol.27 (6), p.783-788

2012

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Impaired insulin sensitivity and secretion in normoglycemic patients with spinocerebellar ataxia type 1

Movement disorders, 2010-09, Vol.25 (12), p.1976-1980

2010

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Depression predicts the pattern of cognitive impairment in early Parkinson's disease

Journal of the neurological sciences, 2006-10, Vol.248 (1), p.131-137

2006

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Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15

Movement disorders, 2010-08, Vol.25 (11), p.1577-1582

2010

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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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Dystonia in Wilson's disease

Movement disorders, 2001-07, Vol.16 (4), p.719-723

2001

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Heterozygous PINK1 mutations: A susceptibility factor for Parkinson disease?

Movement disorders, 2006-09, Vol.21 (9), p.1526-1530

2006

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Homocysteine serum levels and MTHFR C677T genotype in patients with Parkinson's disease, with and without levodopa therapy

Journal of the neurological sciences, 2006-10, Vol.248 (1), p.56-61

2006

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Quality of life in patients with treated and clinically stable Wilson's disease

Movement disorders, 2011-07, Vol.26 (8), p.1503-1508

2011

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Survival of Huntington's disease patients in Serbia: longer survival in female patients

European journal of epidemiology, 2007-08, Vol.22 (8), p.523-526

2007

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Suicide and suicidal ideation in Parkinson's disease

Journal of the neurological sciences, 2010-02, Vol.289 (1), p.40-43

2010

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Prevalence of primary late-onset focal dystonia in the Belgrade population

Movement disorders, 2003-11, Vol.18 (11), p.1389-1392

2003

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Transcranial sonography in pantothenate kinase-associated neurodegeneration

Journal of neurology, 2012-05, Vol.259 (5), p.959-964

2012

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Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients

Movement disorders, 2006-02, Vol.21 (2), p.187-191

2006

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Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification

Journal of neurology, 2011-09, Vol.258 (9), p.1637-1642

2011

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The topography of brain damage at different stages of Parkinson's disease

ATP13A2 variants in early-onset Parkinson's disease patients and controls

Mild cognitive impairment in Parkinson's disease is associated with a distributed pattern of brain white matter damage

Quality of life in patients with focal dystonia

Gait characteristics in patients with major depression performing cognitive and motor tasks while walking

Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation

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

Safety and efficacy of perampanel in advanced Parkinson's disease: A randomized, placebo-controlled study

MRI measurements of brainstem structures in patients with Richardson's syndrome, progressive supranuclear palsy-parkinsonism, and Parkinson's disease

Bcl-2: Prolonging Life in a Transgenic Mouse Model of Familial Amyotrophic Lateral Sclerosis

Status dystonicus: Predictors of outcome and progression patterns of underlying disease

Impaired insulin sensitivity and secretion in normoglycemic patients with spinocerebellar ataxia type 1

Depression predicts the pattern of cognitive impairment in early Parkinson's disease

Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15

Spread of primary dystonia in relation to initially affected region

Dystonia in Wilson's disease

Heterozygous PINK1 mutations: A susceptibility factor for Parkinson disease?

Homocysteine serum levels and MTHFR C677T genotype in patients with Parkinson's disease, with and without levodopa therapy

Quality of life in patients with treated and clinically stable Wilson's disease

Survival of Huntington's disease patients in Serbia: longer survival in female patients

Suicide and suicidal ideation in Parkinson's disease

Prevalence of primary late-onset focal dystonia in the Belgrade population

Transcranial sonography in pantothenate kinase-associated neurodegeneration

Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients

Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification

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