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Tracking Cortical Changes Throughout Cognitive Decline in Parkinson's Disease

Movement disorders, 2020-11, Vol.35 (11), p.1987-1998

2020

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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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Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

Movement disorders, 2016-04, Vol.31 (4), p.436-457

2016

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Longitudinal White Matter Damage Evolution in Parkinson's Disease

Movement disorders, 2022-02, Vol.37 (2), p.315-324

2022

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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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Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force

Movement disorders, 2017-05, Vol.32 (5), p.724-725

2017

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HPCA-related dystonia: Too rare to be found?

Movement disorders, 2016-07, Vol.31 (7), p.1071-1071

2016

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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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Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia

Movement disorders, 2016-12, Vol.31 (12), p.1929-1931

2016

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Brain Structural Changes in Focal Dystonia—What About Task Specificity? A Multimodal MRI Study

Movement disorders, 2021-01, Vol.36 (1), p.196-205

2021

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De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient

Movement disorders, 2014-08, Vol.29 (9), p.1190-1193

2014

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

Movement disorders, 2011-07, Vol.26 (8), p.1575-1576

2011

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Therapeutic efficacy of bilateral prefrontal slow repetitive transcranial magnetic stimulation in depressed patients with Parkinson's disease: An open study

Movement disorders, 2002-05, Vol.17 (3), p.528-532

2002

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Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force

Movement disorders, 2017-05, Vol.32 (5), p.724-725

2017

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Multiple rhythmic movement disorders in a teenage boy with excellent response to clonazepam

Movement disorders, 2008-04, Vol.23 (5), p.767-768

2008

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The first cinematic presentation of a possible rhythmic movement disorder in a Disney film precedes its scientific debut by 60 years

Movement disorders, 2009-01, Vol.24 (1), p.143-144

2009

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Penicillamine-induced lethal status dystonicus in a patient with Wilson's disease

Movement disorders, 2001-05, Vol.16 (3), p.568-569

2001

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N omenclature of genetic movement disorders: R ecommendations of the international P arkinson and movement disorder society task force

Movement disorders, 2016-04, Vol.31 (4), p.436-457

2016

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Reply letter to Jinnah "Locus pocus" and Albanese "Complex dystonia is not a category in the new 2013 consensus classification": Necessary evolution, no magic

Movement disorders, 2016-11, Vol.31 (11), p.1760-1762

2016

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Reply: Bilateral chorea-ballism associated with hyperthyroidism

Movement disorders, 2005-04, Vol.20 (4), p.512-512

Kostic, Vladimir S.

2005

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HPCA -related dystonia: Too rare to be found?: HPCA Mutation Screening

Movement disorders, 2016-07, Vol.31 (7), p.1071-1071

2016

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Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia: ANO10 Mutations in Romani Families

Movement disorders, 2016-12, Vol.31 (12), p.1929-1931

2016

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Tracking Cortical Changes Throughout Cognitive Decline in Parkinson's Disease

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

Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force

Longitudinal White Matter Damage Evolution in Parkinson's Disease

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

Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force

HPCA-related dystonia: Too rare to be found?

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

Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia

Brain Structural Changes in Focal Dystonia—What About Task Specificity? A Multimodal MRI Study

De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient

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

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

A critique of the second consensus criteria for multiple system atrophy

Therapeutic efficacy of bilateral prefrontal slow repetitive transcranial magnetic stimulation in depressed patients with Parkinson's disease: An open study

Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force

Multiple rhythmic movement disorders in a teenage boy with excellent response to clonazepam

The first cinematic presentation of a possible rhythmic movement disorder in a Disney film precedes its scientific debut by 60 years

Penicillamine-induced lethal status dystonicus in a patient with Wilson's disease

N omenclature of genetic movement disorders: R ecommendations of the international P arkinson and movement disorder society task force

Reply letter to Jinnah "Locus pocus" and Albanese "Complex dystonia is not a category in the new 2013 consensus classification": Necessary evolution, no magic

Reply: Bilateral chorea-ballism associated with hyperthyroidism

HPCA -related dystonia: Too rare to be found?: HPCA Mutation Screening

Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia: ANO10 Mutations in Romani Families

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