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Naslov Association Between Substantia Nigra Hyperechogenicity and Central Macular Thickness in Parkinson's Disease (Article)
Autori Svetel Marko  Spaic Dragan  Mijajlovic Milija D  Maric Gorica D  Bozic Marija M  Vasilijevic Jelena B  Dimitrijevic Ana M  Milutinovic Vladimir  Avram Nada  Svetel Marina V 
Info BIOMEDICINES, (2026), vol. 14 br. 7, str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Expanding the differential diagnosis of MSA: A systematic review on dysautonomia in genetic movement disorders (Meeting Abstract)
Autori Lazic Una  Milovanovic A  Damjanovic Radomir  Svetel Marina V  Kostic V  Dragasevic-Miskovic Natasa T  Stankovic I 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2026), vol. 33 br. , Suppl. 1, str. -
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati:
Naslov Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethality (Article)
Autori Magrinelli Francesca  ...  Svetel Marina V  ...  (broj koautora 92) 
Info NATURE COMMUNICATIONS, (2026), vol. 17 br. 1, str. -
Projekat DH | National Institute for Health Research (NIHR) [BRC1287/TN/FM/101410]; Michael J. Fox Foundation for Parkinson's Research (Michael J. Fox Foundation) [MJFF-023893]; American Parkinson Disease Association (American Parkinson Disease Association, Inc.) [1282403]; Parkinson's UK [G-2401]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Enrichment of Rare Variants in Nuclear-Encoded Mitochondrial Metabolism Genes in Patients with Early-Onset or Familial Parkinson's Disease (Article)
Autori Bergant Gaber  ...  Brankovic Marija  Jankovic Milena Z  Svetel Marina V  ...  Dragasevic-Miskovic Natasa T  Petrovic Igor N  ...  Novakovic Ivana V  ...  (broj koautora 19) 
Info GENES, (2026), vol. 17 br. 4, str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Retinal Thickness Profiles in Parkinsonian Syndromes: Discerning Parkinson's Disease, Multiple System Atrophy, and Progressive Supranuclear Palsy via Optical Coherence Tomography (Article)
Autori Svetel Marko  Maric Gorica D  Bozic Marija M  Pekmezovic Tatjana D  Petrovic Igor N  Jaksic Jana  Dimitrijevic Ana M  Lazic Una  Kostic Smiljana  Knezevic Milica  Petrovic Tiana  Petrovic Pajic Sanja MI  Sobot Vesna R  Vasilijevic Jelena B  Svetel Marina V 
Info BIOMEDICINES, (2026), vol. 14 br. 1, str. -
Projekat Project of Institutional Financing of the Faculty of Medicine, University of Belgrade [451-03-66/2024-03/200110]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Biallelic RFC1 expansions as a rare cause of familial and early onset Parkinson's disease in the Slavic population (Meeting Abstract)
Autori Kovanda Anja  Susmelj Lara  Lukezic Tadeja  Maver Ales  Racki Valentino  Vuletic Vladimira  Svetel Marina V  Novakovic Ivana V  Peterlin Borut 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 797-798
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Multi-Center National Study of Genotype-Phenotype Correlation and Clinical Characteristics in Children and Young Adults with Friedreich's Ataxia from Serbia (Article)
Autori Kovacevic Gordana S  Todorovic Slobodanka  Novakovic Ivana V  Dobricic Valerija S  Savic-Pavicevic Dusanka Lj  Milic-Rasic Vedrana M  Svetel Marina V  Brkusanin Milos  Vukomanovic Vladislav A  Vucinic Dragana M  Ostojic Slavica B  Putnik Jovana  Kosac Ana P 
Info BIOMEDICINES, (2025), vol. 13 br. 11, str. -
Projekat the Ministry of Education, Science and Technological Development of the Republic of Serbia, Institutional Funding Program [451-03-66/2024-03/200178]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease (Editorial Material; Early Access)
Autori Kovanda Anja  Susmelj Lara  Jaklic Helena  Lukezic Tadeja  Maver Ales  Petrovic Igor N  Dragasevic-Miskovic Natasa T  Svetel Marina V  Racki Valentino  Vuletic Vladimira  Novakovic Ivana V  Peterlin Borut 
Info CLINICAL GENETICS, (2025), vol. br. , str. -
Projekat Slovenian Research and Innovation Agency (ARIS) [P3-0326, J3-4517]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Is GBA1 mutation status a game-changer for impulse control behaviour in Parkinson's disease? (Article; Early Access)
Autori Kresojevic Nikola D  Markovic Vladana V  Geratovic Cveta  Jecmenica-Lukic Milica V  Tomic Aleksandra D  Dobricic Valerija S  Stankovic Iva D  Stojkovic Tanja  Dragasevic Natasa T  Sarcevic Maksim  Jankovic Milena Z  Marjanovic Ana  Novakovic Ivana V  Kostic Vladimir K  Svetel Marina V  Petrovic Igor N 
Info NEUROLOGICAL SCIENCES, (2025), vol. br. , str. -
Projekat Ministry of Science, Technological development and innovation of Republic of Serbia; Faculty of Medicine, University of Belgrade, Serbia [451-03-65/2024-03/200110]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov The role of genetic factors in the occurrence of levodopa-induced motor complications in Parkinson's disease (Article; Early Access)
Autori Radojevic Branislava  Milovanovic Andona  Petrovic Igor N  Svetel Marina V  Marjanovic Ana  Jancic Ivan R  Stanisavljevic Dejana M  Milicevic Ognjen S  Savic Miroslav M  Kostic Vladimir S  Dragasevic-Miskovic Natasa T 
Info NEUROLOGICAL RESEARCH, (2025), vol. br. , str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
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