Search Results - "Petrović, Igor N."

Brain Calcification and Movement Disorders by Kostic, Vladimir S, Petrovic, Igor N

“…Brain calcifications may be an incidental finding on neuroimaging in normal, particularly older individuals, but can also indicate numerous hereditary and…”
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Zolpidem improves task-specific dystonia: A randomized clinical trial integrating exploratory transcranial magnetic stimulation and [18F] FDG-PET imaging by Vogelnik Žakelj, Katarina, Trošt, Maja, Tomše, Petra, Petrović, Igor N., Tomić Pešić, Aleksandra, Radovanović, Saša, Kojović, Maja

“…Task-specific dystonia (TSFD) is a disabling movement disorder. Effective treatment options are currently limited. Zolpidem was reported to improve primary…”
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Tracking brain damage in progressive supranuclear palsy: a longitudinal MRI study by Agosta, Federica, Caso, Francesca, Ječmenica-Lukić, Milica, Petrović, Igor N, Valsasina, Paola, Meani, Alessandro, Copetti, Massimiliano, Kostić, Vladimir S, Filippi, Massimo

“…ObjectivesIn this prospective, longitudinal, multiparametric MRI study, we investigated clinical as well as brain grey matter and white matter (WM) regional…”
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Clinical outcomes of two main variants of progressive supranuclear palsy and multiple system atrophy: a prospective natural history study by Jecmenica-Lukic, Milica, Petrovic, Igor N., Pekmezovic, Tatjana, Kostic, Vladimir S.

“…Progressive supranuclear palsy (PSP) and parkinsonian subtype of multiple system atrophy (MSA-P) are, after Parkinson’s disease (PD), the most common forms of…”
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Mitochondrial myopathy, encephalopathy, lactate acidosis with stroke-like episodes syndrome (MELAS): a case report by Petrović, Igor N, Mandić, Gorana, Svetel, Marina, Dragašević, Nataša, Lačković, Vesna, Kostić, Vladimir S

“…Mitochondrial encephalopathy, lactacidosis and stroke-like episodes (MELAS) represent a multisystemic dysfunction due to various mutations in mitochondrial…”
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Use of the Neuropsychiatric Inventory to Characterize the Course of Neuropsychiatric Symptoms in Progressive Supranuclear Palsy by Ječmenica-Lukić, Milica, Pekmezović, Tatjana, Petrović, Igor N, Tomić, Aleksandra, Svetel, Marina, Kostić, Vladimir S

“…The aim of this study was to determine the neuropsychiatric profile in a cohort of progressive supranucelar palsy (PSP) patients and their dynamic changes over…”
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Characteristics of two distinct clinical phenotypes of functional (psychogenic) dystonia: follow-up study by Petrović, Igor N., Tomić, Aleksandra, Vončina, Marija Mitković, Pešić, Danilo, Kostić, Vladimir S.

“…Background The fixed dystonia phenotype was originally established as a prototype of functional dystonia. Nevertheless, in recent reports different functional…”
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Superficial siderosis: case report and literature review by Kresojevic, Nikola, Petrovic, Igor, Dragasevic­Miskovic, Natasa, Kostic, Vladimir

“…Superficial siderosis (SS) is caused by chronic subarachnoid bleeding and is characterized by free iron and hemosiderin deposition along the pial and subpial…”
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Case report: Rapid-onset parkinsonism after a hornet sting by Tomic, Svetlana, Zjalic, Milorad, Popovic, Zvonimir, Krivdic Dupan, Zdravka, Heffer, Marija, Snajder Mujkic, Darija, Mandic, Dario, Guljas, Silva, Petrovic, Igor N

“…Neurological manifestations with basal ganglia involvement following stings are rare and clinically ill-defined conditions. We present a patient with acute…”
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Minimal change multiple system atrophy: An aggressive variant? by Ling, Helen, Asi, Yasmine T., Petrovic, Igor N., Ahmed, Zeshan, Prashanth, L. K., Hazrati, Lili-Naz, Nishizawa, Masatoyo, Ozawa, Tetsutaro, Lang, Anthony, Lees, Andrew J., Revesz, Tamas, Holton, Janice L.

“…ABSTRACT Background Glial cytoplasmic inclusions containing α‐synuclein are the pathological hallmark of multiple system atrophy (MSA). Minimal change (MC‐MSA)…”
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Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population by Janković, Milena Z, Kresojević, Nikola D, Dobričić, Valerija S, Marković, Vladana V, Petrović, Igor N, Novaković, Ivana V, Kostić, Vladimir S

“…Abstract Background Mutations in LRRK2 (leucine-rich repeat kinase 2) are the most common cause of autosomal dominant Parkinson's disease (PD). Large…”
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Mutation screening of the DYT6/THAP1 gene in Serbian patients with primary dystonia by Dobričić, Valerija S., Kresojević, Nikola D., Svetel, Marina V., Janković, Milena Z., Petrović, Igor N., Tomić, Aleksandra D., Novaković, Ivana V., Kostić, Vladimir S.

“…Primary dystonia (PrD) is characterized by sustained muscle contractions, causing twisting and repetitive movements and abnormal postures. Besides DYT1/ TOR1A…”
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MM2 subtype of sporadic Creutzfeldt-Jakob disease may underlie the clinical presentation of progressive supranuclear palsy by Petrovic, Igor N., Martin-Bastida, Antonio, Massey, Luke, Ling, Helen, O’Sullivan, Sean S., Williams, David R., Holton, Janice L., Revesz, Tamas, Ironside, James W., Lees, Andrew J., Silveira-Moriyama, Laura

“…The classical presentation of sporadic Creutzfeldt-Jakob disease (sCJD) is rapid progressive dementia often associated with myoclonus and ataxia followed by…”
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Characteristic “Forcible” Geste Antagoniste in Oromandibular Dystonia Resulting From Pantothenate Kinase‐Associated Neurodegeneration by Petrović, Igor N., Kresojević, Nikola, Ganos, Christos, Svetel, Marina, Dragašević, Nataša, Bhatia, Kailash P., Kostić, Vladimir S.

“…Geste antagonistes are usually considered typical of primary dystonia, although rarely they have been described in secondary/heredodegenerative dystonias. We…”
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Cognitive impairment and structural brain damage in multiple system atrophy-parkinsonian variant by Caso, Francesca, Canu, Elisa, Lukic, Milica Jecmenica, Petrovic, Igor N., Fontana, Andrea, Nikolic, Ivan, Kostic, Vladimir S., Filippi, Massimo, Agosta, Federica

“…In this multiparametric, cross-sectional study, we aimed to investigate cognitive impairment and brain structural changes in patients with multiple system…”
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The Profile and Evolution of Neuropsychiatric Symptoms in Multiple System Atrophy: Self- and Caregiver Report by Jecmenica-Lukic, Milica, Petrovic, Igor N, Pekmezovic, Tatjana, Tomic, Aleksandra, Stankovic, Iva, Svetel, Marina, Kostic, Vladimir S

“…Objective: Recent research shows that patients with multiple system atrophy (MSA) have significant cognitive and neuropsychiatric comorbidities that can color…”
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Functional MRI connectivity of the primary motor cortex in functional dystonia patients by Piramide, Noemi, Sarasso, Elisabetta, Tomic, Aleksandra, Canu, Elisa, Petrovic, Igor N., Svetel, Marina, Basaia, Silvia, Dragasevic Miskovic, Natasa, Kostic, Vladimir S., Filippi, Massimo, Agosta, Federica

“…Background Functional movement disorders include a wide spectrum of clinically documented movement disorders without an apparent organic substrate. Objective…”
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Multiple system atrophy-parkinsonism with slow progression and prolonged survival: A diagnostic catch by Petrovic, Igor N., Ling, Helen, Asi, Yasmine, Ahmed, Zeshan, Kukkle, Prashanth L., Hazrati, Lili-Naz, Lang, Anthony E., Revesz, Tamas, Holton, Janice L., Lees, Andrew J.

“…Background: Multiple system atrophy (MSA) is a neurodegenerative disease leading to severe physical impairment, with a disease duration from onset to death of…”
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White matter lesions and depression in patients with Parkinson's disease by Petrovic, Igor N, Stefanova, Elka, Kozic, Dusko, Semnic, Robert, Markovic, Vladana, Daragasevic, Natasa T, Kostic, Vladimir S

“…Abstract Depression is frequently associated with Parkinson disease (PD) but neural basis is still unclear. In previous studies white matter changes present as…”
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Factors associated with deterioration of health-related quality of life in multiple system atrophy: 1-year follow-up study by Jecmenica-Lukic, Milica V., Pekmezovic, Tatjana D., Petrovic, Igor N., Dragasevic, Natasa T., Kostić, Vladimir S.

“…The aim of this study was to identify the main contributors to the health-related quality of life (HRQoL) in multiple system atrophy with predominant…”
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