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73 results for Kostić,+Vladimir+S

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ArticlesPeer ReviewedFull Text
Artificial intelligence for assisting diagnostics and assessment of Parkinson’s disease—A review
Author / Creator:Belić, Minja ; Bobić, Vladislava ; Badža, Milica ; Šolaja, Nikola ; Đurić-Jovičić, Milica ; Kostić, Vladimir S
Publisher:Netherlands: Elsevier B.V
Journal title:Clinical neurology and neurosurgery, 2019-09, Vol.184, p.105442-105442, Article 105442
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Prevalence of non-motor symptoms in young-onset versus late-onset Parkinson’s disease
Author / Creator:Špica, Vladana ; Pekmezović, Tatjana ; Svetel, Marina ; Kostić, Vladimir S.
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Journal of neurology, 2013-01, Vol.260 (1), p.131-137
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An Expert System for Quantification of Bradykinesia Based on Wearable Inertial Sensors
Author / Creator:Bobić, Vladislava ; Djurić-Jovičić, Milica ; Dragašević, Nataša ; Popović, Mirjana B. ; Kostić, Vladimir S. ; Kvaščev, Goran
Publisher:Switzerland: MDPI AG
Journal title:Sensors (Basel, Switzerland), 2019-06, Vol.19 (11), p.2644
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Structural brain heterogeneity underlying symptomatic and asymptomatic genetic dystonia: a multimodal MRI study
Author / Creator:Tomić, Aleksandra ; Sarasso, Elisabetta ; Basaia, Silvia ; Dragašević-Misković, Nataša ; Svetel, Marina ; Kostić, Vladimir S. ; Filippi, Massimo ; Agosta, Federica
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2024-04, Vol.271 (4), p.1767-1775
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C9orf72 expansion as a possible genetic cause of Huntington disease phenocopy syndrome
Author / Creator:Kostić, Vladimir S. ; Dobričić, Valerija ; Stanković, Iva ; Ralić, Vesna ; Stefanova, Elka
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2014-10, Vol.261 (10), p.1917-1921
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ArticlesPeer ReviewedFull Text
Autosomal recessive adult onset ataxia
Author / Creator:Dragašević-Mišković, Nataša ; Stanković, Iva ; Milovanović, Andona ; Kostić, Vladimir S.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2022-01, Vol.269 (1), p.504-533
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ArticlesPeer ReviewedFull Text
Quantification of Finger-Tapping Angle Based on Wearable Sensors
Author / Creator:Djurić-Jovičić, Milica ; Jovičić, Nenad ; Roby-Brami, Agnes ; Popović, Mirjana ; Kostić, Vladimir ; Djordjević, Antonije
Publisher:Switzerland: MDPI AG
Journal title:Sensors (Basel, Switzerland), 2017-01, Vol.17 (2), p.203-203
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Clinical, cognitive, and behavioural correlates of white matter damage in progressive supranuclear palsy
Author / Creator:Agosta, Federica ; Galantucci, Sebastiano ; Svetel, Marina ; Lukić, Milica Ječmenica ; Copetti, Massimiliano ; Davidovic, Kristina ; Tomić, Aleksandra ; Spinelli, Edoardo G. ; Kostić, Vladimir S. ; Filippi, Massimo
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2014-05, Vol.261 (5), p.913-924
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Glucocerebrosidase and parkinsonism: lessons to learn
Author / Creator:Markovic, Ivanka ; Kresojevic, Nikola ; Kostic, Vladimir S
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2016-05, Vol.263 (5), p.1033-1044
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Adherence to Medication among Parkinson’s Disease Patients Using the Adherence to Refills and Medications Scale
Author / Creator:Radojević, Branislava ; Dragašević-Mišković, Nataša T. ; Milovanović, Andona ; Svetel, Marina ; Petrović, Igor ; Pešić, Maja ; Tomić, Aleksandra ; Stanisavljević, Dejana ; Savić, Miroslav M. ; Kostić, Vladimir S.
Publisher:India: Hindawi
Journal title:International journal of clinical practice (Esher), 2022-02, Vol.2022, p.1-7
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Quality of life in patients with progressive supranuclear palsy: one-year follow-up
Author / Creator:Pekmezovic, Tatjana ; Jecmenica-lukic, Milica ; Petrovic, Igor ; Spica, Vladana ; Tomic, Aleksandra ; Kostic, Vladimir S
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2015-09, Vol.262 (9), p.2042-2048
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Clinical course of patients with pantothenate kinase-associated neurodegeneration (PKAN) before and after DBS surgery
Author / Creator:Svetel, Marina ; Tomić, Aleksandra ; Dragašević, Nataša ; Petrović, Igor ; Kresojević, Nikola ; Jech, Robert ; Urgošik, Dušan ; Banjac, Isidora ; Vitković, Jelena ; Novaković, Ivana ; Kostić, Vladimir S.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2019-12, Vol.266 (12), p.2962-2969
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Characteristics of two distinct clinical phenotypes of functional (psychogenic) dystonia: follow-up study
Author / Creator:Petrović, Igor N. ; Tomić, Aleksandra ; Vončina, Marija Mitković ; Pešić, Danilo ; Kostić, Vladimir S.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2018-01, Vol.265 (1), p.82-88
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Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience
Author / Creator:Kresojević, Nikola ; Dobričić, Valerija ; Lukić, Milica Ječmenica ; Tomić, Aleksandra ; Petrović, Igor ; Dragašević, Nataša ; Perović, Ivana ; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Novaković, Ivana ; Svetel, Marina ; Kostić, Vladimir S.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2022-06, Vol.269 (6), p.3167-3174
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Mutations in THAP1 ( DYT6 ) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study
Author / Creator:Djarmati, Ana, PhD ; Schneider, Susanne A, MD ; Lohmann, Katja, PhD ; Winkler, Susen, BSc ; Pawlack, Heike, BSc ; Hagenah, Johann, MD ; Brüggemann, Norbert, MD ; Zittel, Simone, MD ; Fuchs, Tania, PhD ; Raković, Aleksandar, MSc ; Schmidt, Alexander, MD ; Jabusch, Hans-Christian, MD ; Wilcox, Robert, MD ; Kostić, Vladimir S, MD ; Siebner, Hartwig, MD ; Altenmüller, Eckart, MD ; Münchau, Alexander, MD ; Ozelius, Laurie J, PhD ; Klein, Christine, MD
Publisher:England: Elsevier Limited
Journal title:Lancet neurology, 2009-05, Vol.8 (5), p.447-452
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ArticlesPeer ReviewedFull Text
Transcranial midbrain sonography and depressive symptoms in patients with Parkinson’s disease
Author / Creator:Stanković, Iva ; Stefanova, Elka ; Žiropadja, Ljubomir ; Mijajlović, Milija ; Pavlović, Aleksandra ; Kostić, Vladimir S.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2015-03, Vol.262 (3), p.689-695
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Transcranial sonography in pantothenate kinase-associated neurodegeneration
Author / Creator:Kostić, Vladimir S. ; Svetel, Marina ; Mijajlović, Milija ; Pavlović, Aleksandra ; Ječmenica-Lukić, Milica ; Kozić, Dušan
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Journal of neurology, 2012-05, Vol.259 (5), p.959-964
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Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients
Author / Creator:Mitropoulos, Konstantinos ; Merkouri Papadima, Eleni ; Xiromerisiou, Georgia ; Balasopoulou, Angeliki ; Charalampidou, Kyriaki ; Galani, Vasiliki ; Zafeiri, Krystallia-Vassiliki ; Dardiotis, Efthymios ; Ralli, Styliani ; Deretzi, Georgia ; John, Anne ; Kydonopoulou, Kyriaki ; Papadopoulou, Elpida ; di Pardo, Alba ; Akcimen, Fulya ; Loizedda, Annalisa ; Dobričić, Valerija ; Novaković, Ivana ; Kostić, Vladimir S. ; Mizzi, Clint ; Peters, Brock A. ; Basak, Nazli ; Orrù, Sandro ; Kiskinis, Evangelos ; Cooper, David N. ; Gerou, Spyridon ; Drmanac, Radoje ; Bartsakoulia, Marina ; Tsermpini, Evangelia-Eirini ; Hadjigeorgiou, Georgios M. ; Ali, Bassam R. ; Katsila, Theodora ; Patrinos, George P.
Publisher:England: BioMed Central
Journal title:Human genomics, 2017-12, Vol.11 (1), p.30-30, Article 30
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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
Author / Creator:Kostić, Vladimir S. ; Lukić-Ječmenica, Milica ; Novaković, Ivana ; Dobričić, Valerija ; Brajković, Lela ; Krajinović, Maja ; Klein, Christine ; Pavlović, Aleksandra
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Journal of neurology, 2011-09, Vol.258 (9), p.1637-1642
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Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia
Author / Creator:Dobričić, Valerija S. ; Kresojević, Nikola D. ; Svetel, Marina V. ; Janković, Milena Z. ; Petrović, Igor N. ; Tomić, Aleksandra D. ; Novaković, Ivana V. ; Kostić, Vladimir S.
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Journal of neurology, 2013-04, Vol.260 (4), p.1037-1042
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Showing 1 to 20 of 73 results

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Artificial intelligence for assisting diagnostics and assessment of Parkinson’s disease—A review

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

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An Expert System for Quantification of Bradykinesia Based on Wearable Inertial Sensors

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

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

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Autosomal recessive adult onset ataxia

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Quantification of Finger-Tapping Angle Based on Wearable Sensors

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

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Glucocerebrosidase and parkinsonism: lessons to learn

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Adherence to Medication among Parkinson’s Disease Patients Using the Adherence to Refills and Medications Scale

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

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

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

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

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Mutations in THAP1 ( DYT6 ) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study

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

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Transcranial sonography in pantothenate kinase-associated neurodegeneration

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Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients

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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

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Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia

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