Researchers

Results 81-100 of 555
ГодинаНасловАутор(и)Тип резултатаМп-кат.
2020Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1β, andTNF-α in relation with Parkinson’s disease progressionPešić, Milica  ; Maksimović, Nela  ; Aleksić, A.; Gulić, Milica ; Đuranović, Ana  ; Grk, Milka  ; Dušanović-Pjević, Marija  ; Stanković, Iva ; Marković, Vladana  ; Marjanović, Ana ;
Novaković, Ivana  ; Dragašević-Mišković, Nataša  ; Kostić, Vladimir S. ;
Conference Paper
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2020Longitudinal clinical and neuroanatomical changes of PD-MCI RevertersDonzuso, Giulia; Agosta, Federica; Canu, Elisa; Stojković, Tanja  ; Basaia, Silvia; Stanković, Iva D. ; Tomić, Aleksandra D.  ; Stefanova, Elka D. ; Marković, Vladana V.  ; Kostić, Vladimir S. ;
Filippi, Massimo;
Conference Paper
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2020Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic NeuropathyDawod, Phepy G. A.; Jančić, Jasna  ; Marjanović, Ana ; Branković, Marija  ; Janković, Milena ; Samardžić, Janko  ; Potkonjak, Dario ; Đurić, Vesna; Mesaroš, Šarlota  ; Novaković, Ivana  ;
Abdel Motaleb, Fayda I.; Kostić, Vladimir S. ; Nikolić, Dejan  ;
Article
21M21
2020Novel PANK2 mutation identified in a patient with pantothenate kinase-associated neurodegenerationSvetel, Marina V. ; Novakovic, Ivana V.  ; Tomić, Svetlana; Kresojević, Nikola D. ; Kostić, Vladimir K. Article
23M23
2020Comparison of dystonic and essential tremor: clinical and quantitative assessmentJovanović, Čarna; Berbakov, Lazar  ; Svetel, Marina V. ; Petrović, Igor N.  ; Dragašević, Nataša T.  ; Pekmezović, Tatjana D.  ; Kostić, Vladimir K. Conference Paper
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2020Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1 ss, andTNF-alpha in relation with Parkinson's disease progressionPešić, Milica  ; Maksimović, Nela S.  ; Aleksić, Anđelka; Gulić, Milica ; Đuranović, Ana S.  ; Grk, Milka B.  ; Dušanović-Pjević, Marija G.  ; Stanković, Iva D. ; Marković, Vladana V.  ; Marjanović, Ana ;
Novaković, Ivana V.  ; Dragašević-Mišković, Nataša T.  ; Kostić, Vladimir S. ;
Conference Paper
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2020Longitudinal evolution of white matter damage in Parkinson's diseaseScamarcia, Pietro Giuseppe; Agosta, Federica; Spinelli, Edoardo Gioele; Stojković, Tanja  ; Pagani, Elisabetta; Stanković, Iva D. ; Marković, Vladana V.  ; Petrović, Igor N.  ; Stefanova, Elka D. ; Kostić, Vladimir S. ;
Filippi, Massimo;
Conference Paper
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2020Neurologija : za studente medicineKostić, Vladimir ; Apostolski, Slobodan ; Bulat, Petar  ; Bumbaširević, Ljiljana ; Cerovac-Ćosić, Nataša  ; Dragašević-Mišković, Nataša  ; Jančić, Jasna  ; Jovanović, Dejana  ; Jovanović-Marković, Zagorka ; Jović, Nebojša J. ;
Kozić, Duško  ; Lavrnić, Dragana ; Martinović, Žarko; Milić-Rašić, Vedrana ; Drulović, Jelena ; Ocić, Gordana ; Pavlović, Dragan M. ; Rakočević-Stojanović, Vidosava ; Sokić, Dragoslav  ; Stefanova, Elka ; Stević, Zorica ; Stošić-Opinćal, Tatjana ; Svetel, Marina ; Čovičković-Šternić, Nadežda ; Pavlović, Slobodan; Todorović, Slobodanka ; Zidverc Trajković, Jasna ; Novaković, Ivana  ; Vojvodić, Nikola M.  ; Mesaroš, Šarlota  ; Pavlović, Aleksandra  ; Basta, Ivana  ; Dujmović Bašuroski, Irena; Ristić, Aleksandar  ; Ercegovac, Marko  ; Mijajlović, Milija  ; Kačar, Aleksandra  ; Petrović, Igor  ; Radojičić, Aleksandra  ; Berisavac, Ivana  ; Nikolić, Ana;
Text book
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2020Very Late-Onset Niemann Pick Type C Disease: Example of Progressive Supranuclear Palsy Look-Alike DisorderKresojević, Nikola D. ; Mandić-Stojmenović, Gorana B.  ; Dobričić, Valerija S. ; Petrović, Igor N.  ; Brajković, Leposava D. ; Stefanova, Elka D. ; Svetel, Marina V. ; Kostić, Vladimir K. Article
22M22
2020Analysis of secondary mtDNA mutations in families with Leber's hereditary optic neuropathy: Four novel variants and their association with clinical presentationJančić, Jasna B.  ; Rovčanin, Branislav R.; Đurić, Vesna; Pepić, Ana; Samardžić, Janko S.  ; Nikolić, Blažo  ; Novaković, Ivana V.  ; Kostić, Vladimir S. Article
21M21
2020Changes of Phenotypic Pattern in Functional Movement Disorders: A Prospective Cohort StudyTomić, Aleksandra D.  ; Ječmenica-Lukić, Milica V.  ; Petrović, Igor N.  ; Svetel, Marina V. ; Dragašević-Mišković, Nataša T.  ; Kresojević, Nikola D. ; Marković, Vladana V.  ; Kostić, Vladimir S. Article
21M21
2020In silico model of mtDNA mutations effect on secondary and 3D structure of mitochondrial rRNA and tRNA in Leber's hereditary optic neuropathyRovčanin, Branislav R.  ; Jančić, Jasna B.  ; Samardžić, Janko M.  ; Rovčanin, Marija G.  ; Nikolić, Blažo  ; Ivančević, Nikola  ; Novaković, Ivana V.  ; Kostić, Vladimir K. Article
21aM21a
2019Functional network connectivity predicts spreading of cortical atrophy in Parkinson's diseaseAgosta, Federica; Basaia, Silvia; Zahedmanesh, Homa; Stojković, Tanja  ; Stanković, Iva D. ; Marković, Vladana V.  ; Petrović, Igor N.  ; Stefanova, Elka D. ; Kostić, Vladimir S. ; Filippi, MassimoConference Paper
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2019Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathyDawod, Phepy G. A.; Rovčanin, Branislav R.  ; Branković, Marija  ; Marjanović, Ana ; Janković, Milena Z. ; Novaković, Ivana V.  ; Motaleb, Abdel F.; Jančić, Jasna B.  ; Kostić, Vladimir S. Conference Paper
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2019Correlation of selected polymorphisms in COMT, DAT (SL6A3), DRD2, and ANKK1 genes and complications of long-term levodopa treatment in patients with idiopathic Parkinsons diseaseRadojević, Branislava  ; Dragašević-Mišković, Nataša  ; Marjanović, Ana ; Branković, Marija  ; Dobričić, Valerija ; Milovanović, Andona ; Svetel, Marina ; Petrović, Igor  ; Savić, Miroslav  ; Jančić, Ivan  ;
Novaković, Ivana  ; Kostić, Vladimir S. ;
Conference Paper
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2019Longitudinal cortical changes associated with apathy in Parkinson's diseaseAgosta, Federica; Imperiale, Francesca; Canu, Elisa; Stojković, Tanja  ; Stanković, Iva D. ; Basaia, Silvia; Fontana, Andrea; Marković, Vladana V.  ; Petrović, Igor N.  ; Stefanova, Elka D. ;
Kostić, Vladimir S. ; Filippi, Massimo;
Conference Paper
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2019Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathyDawod, Phepy G. A.; Rovčanin, Branislav R.; Branković, Marija  ; Marjanović, Ana ; Janković, Milena Z. ; Novaković, Ivana V.  ; Dujmović, Irena ; Jančić, Jasna B.  ; Kostić, Vladimir S. Conference Paper
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2019Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patientsMitropoulos, Konstantinos; ...; Dobričić, Valerija S. ; Novaković, Ivana V.  ; Kostić, Vladimir S. ; ...; (broj koautora 33)Conference Paper
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2019Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriersMarjanović, Ana ; Dobričić, Valerija S. ; Branković, Marija  ; Janković, Milena Z. ; Mandić, Gorana B.  ; Stefanova, Elka D. ; Stević, Zorica D. ; Novaković, Ivana V.  ; Kostić, Vladimir S. Conference Paper
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2019Artificial intelligence for assisting diagnostics and assessment of Parkinson's disease-A reviewBelić, Minja; Bobić, Vladislava  ; Badža, Milica  ; Šolaja, Nikola; Đurić-Jovičić, Milica  ; Kostić, Vladimir Reviews
22M22