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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 RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia (Article)
Autori Milovanovic Andona  Dragasevic-Miskovic Natasa T  Thomsen Mirja  Borsche Max  Hinrichs Frauke  Westenberger Ana  Klein Christine  Brueggemann Norbert  Brankovic Marija  Marjanovic Ana  Svetel Marina V  Kostic Vladimir S  Lohmann Katja 
Info MOVEMENT DISORDERS CLINICAL PRACTICE, (2024), vol. 11 br. 6, str. 626-633
Projekat Deutsche Forschungsgemeinschaft; University of Luebeck [FOR 2488]; German Research Foundation
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype (Editorial Material)
Autori Kulikovskaja Leonora  Sarajlija Adrijan  Savic-Pavicevic Dusanka Lj  Dobricic Valerija S  Klein Christine  Westenberger Ana 
Info NEUROLOGY-GENETICS, (2018), vol. 4 br. 2, str. -
Projekat Hermann and Lilly Schilling Foundation; Land Schleswig-Holstein within the funding programme Open Access Publikationsfonds
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia (Article)
Autori Dobricic Valerija S  Tomic Aleksandra D  Brankovic Vesna  Kresojevic Nikola D  Jankovic Milena Z  Westenberger Ana  Milic-Rasic Vedrana M  Klein Christine  Novakovic Ivana V  Svetel Marina V  Kostic Vladimir S 
Info PARKINSONISM & RELATED DISORDERS, (2017), vol. 45 br. , str. 81-84
Projekat Ministry of Education and Science, Republic of Serbia [ON175090, ON175091]; Hermann and Lilly Schilling Foundation; German Research Foundation (DFG) Research Unit [FOR2488]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Seemingly Dominant Inheritance of a Recessive ANO10 Mutation in Romani Families With Cerebellar Ataxia (Letter)
Autori Dragasevic-Miskovic Natasa T  Domingo Aloysius  Dobricic Valerija S  Max Christoph  Braenne Ingrid  Petrovic Igor N  Grutz Karen  Pawlack Heike  Tournev Ivailo  Kalaydjieva Luba  Svetel Marina V  Lohmann Katja  Kostic Vladimir S  Westenberger Ana 
Info MOVEMENT DISORDERS, (2016), vol. 31 br. 12, str. 1929-1931
Projekat Ministry of Education and Science, Republic of Serbia [ON175090]; Medical Genetics Priority Program of the University of Lubeck, Germany; National Research Fund of Ministry of Education and Science of Bulgaria
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited (Article)
Autori Dobricic Valerija S  Kresojevic Nikola D  Zarkovic Milena  Tomic Aleksandra D  Marjanovic Ana  Westenberger Ana  Cvetkovic Dragana D  Svetel Marina V  Novakovic Ivana V  Kostic Vladimir S 
Info PARKINSONISM & RELATED DISORDERS, (2015), vol. 21 br. 10, str. 1256-1259
Projekat Ministry of Education and Science, Republic of Serbia [ON175090, ON175091]; Fritz Thyssen Foundation [Az. 10.14.1.233]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Novel GNAL Mutations in Two German Patients With Sporadic Dystonia (Letter)
Autori Ziegan Julia  Wittstock Matthias  Westenberger Ana  Dobricic Valerija S  Wolters Alexander  Benecke Reiner  Klein Christine  Kamm Christoph 
Info MOVEMENT DISORDERS, (2014), vol. 29 br. 14, str. 1833-1834
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov De Novo Mutation in the GNAL Gene Causing Seemingly Sporadic Dystonia in a Serbian Patient (Article)
Autori Dobricic Valerija S  Kresojevic Nikola D  Westenberger Ana  Svetel Marina V  Tomic Aleksandra D  Ralic Vesna  Petrovic Igor N  Jecmenica-Lukic Milica V  Lohmann Katja  Novakovic Ivana V  Klein Christine  Kostic Vladimir S 
Info MOVEMENT DISORDERS, (2014), vol. 29 br. 9, str. 1190-1193
Projekat Ministry of Education and Science, Republic of Serbia [ON175090, ON175091]; Hermann and Lilly Schilling Foundation
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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