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Autori: Dragasevic-Miskovic Natasa T

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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  
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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