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Autori: Dragasevic-Miskovic Natasa T

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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 Chorea in Hereditary Leukodystrophies - Overview of Two Cases (Article)
Autori Milovanovic Andona  Jecmenica-Lukic Milica V  Mazalica Nina  Radisic Vanja  Djordjevic-Milosevic Maja  Marjanovic Ana  Brankovic Marija  Markovic Vladana V  Kresojevic Nikola D  Kostic Vladimir K  Dragasevic-Miskovic Natasa T 
Info TREMOR AND OTHER HYPERKINETIC MOVEMENTS, (2025), vol. 15 br. , str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Expert commentary for first case of Cayman ataxia far North of the Caribbean: A 20-year-old Inuit male with homozygous deletion in ATCAY gene (Editorial Material)
Autori Milovanovic Andona  Dragasevic-Miskovic Natasa T  Stankovic Iva D 
Info PARKINSONISM & RELATED DISORDERS, (2025), vol. 141 br. , str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Examination of the frequency and characteristics of impulse control disorders in Wilson's disease (Meeting Abstract)
Autori Nikolic A  Markovic V  Kostic V  Dragasevic-Miskovic Natasa T  Petrovic Igor N  Jecmenica-Lukic Milica V  Stankovic-Tutus I  Tomic-Pesic Aleksandra  Kresojevic Nikola D 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2025), vol. 32 br. , Suppl. 1, str. -
Ispravka ISI/Web of Science   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 FGF14 repeat length and mosaic interruptions: modifiers of spinocerebellar ataxia 27B? (Article; Early Access)
Autori Lass Joshua  ...  Milovanovic Andona  ...  Dragasevic-Miskovic Natasa T  ...  (broj koautora 18) 
Info BRAIN, (2025), vol. br. , str. -
Projekat German Research Foundation [2025]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
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:
Naslov An Unusual Presentation of a DNMT1 Mutation: Progressive Supranuclear Palsy Look-Alike Disorder (Editorial Material; Early Access)
Autori Jecmenica-Lukic Milica V  Milovanovic Andona  Mazalica Nina  Westenberger Ana  Tomic-Pesic Aleksandra  Petrovic Igor N  Markovic Vladana V  Kresojevic Nikola D  Klein Christine  Kostic Vladimir S  Dragasevic-Miskovic Natasa T 
Info MOVEMENT DISORDERS CLINICAL PRACTICE, (2025), vol. br. , str. -
Projekat German Research Foundation
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Reply to: "Two Families with ANO10-Related Spinocerebellar Ataxia with Novel Exon Deletions: A First Report from India" (Letter; Early Access)
Autori Milovanovic Andona  Westenberger Ana  Dragasevic-Miskovic Natasa T 
Info MOVEMENT DISORDERS, (2025), vol. br. , str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Sleep problems in female carriers of premutation in the FMR1 gene (Meeting Abstract)
Autori Pesic Milica  Stevanovic Milena  Andrejic Nikola  Pesovic Jovan  Cirkovic Sanja S  Dimitrijevic Sanja S  Bascarevic Danijela  Dragasevic-Miskovic Natasa T  Novakovic Ivana V  Protic Dragana D 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1088-1088
Projekat [2024 FX2020-DP-BG-001]
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
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