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Autori: Dobricic Valerija S

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Naslov Selected genetic polymorphisms of COMT, DRD2, ANKK1, and DAT genes and the risk of psychosis in Parkinson's disease (Meeting Abstract)
Autori Radojevic B Dragasevic Natasa T Milovanovic A Brankovic Marija  Svetel Marina V  Dobricic Valerija S Petrovic Igor N Savic M Stanisavljevic Dejana M  Kostic Vladimir K 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2021), vol. 28 br. , Suppl. 1, str. 352-352
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice (Article)
Autori Messerschmidt Clemens ... Pavlovic Aleksandra M  Kostic Vladimir K Dobricic Valerija S ... (broj koautora 34) 
Info SCIENTIFIC REPORTS, (2021), vol. 11 br. 1, str. -
Projekat BIH
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism (Article)
Autori Pesic Milica  Dragasevic-Miskovic Natasa T Marjanovic Ana  Dobricic Valerija S Maksimovic Nela S  Svetel Marina V  Perovic Dijana  Novakovic Ivana V  Cirkovic Sanja Stankovic Iva D  Kostic Vladimir K 
Info NEUROLOGICAL RESEARCH, (2021), vol. 43 br. 4, str. 321-326
Projekat Ministry of education, science and technological development of Serbia [175090]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies (Article)
Autori Maksic Jasmina  Dobricic Valerija S Rasulic Lukas G  Maksimovic Nela S  Brankovic Marija  Milic-Rasic Vedrana M Rakocevic-Stojanovic Vidosava M Novakovic Ivana V  
Info VOJNOSANITETSKI PREGLED, (2020), vol. 77 br. 4, str. 387-394
Projekat Serbian Ministry of Education, Science and Technological Development [175083, 175091]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Very Late-Onset Niemann Pick Type C Disease: Example of Progressive Supranuclear Palsy Look-Alike Disorder (Editorial Material)
Autori Kresojevic Nikola D  Mandic-Stojmenovic Gorana B Dobricic Valerija S Petrovic Igor N Brajkovic Leposava D Stefanova Elka D  Svetel Marina V  Kostic Vladimir K 
Info MOVEMENT DISORDERS CLINICAL PRACTICE, (2020), vol. 7 br. 2, str. 211-214
Projekat Ministry of Education, Science, and Technological Development of the Republic of Serbia [175090]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Significance of KIT and PDGFRA mutations in gastric gastrointestinal stromal tumor imatinib-naive surgically treated patients (Article)
Autori Ebrahimi Keramatollah Sabljak Predrag V Simic Aleksandar P  Skrobic Ognjan M Velickovic Dejan  Sljukic Vladimir M Novakovic Ivana V  Dobricic Valerija S Micev Marjan T Pasko Predrag 
Info VOJNOSANITETSKI PREGLED, (2019), vol. 76 br. 12, str. 1268-1273
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers (Meeting Abstract)
Autori Marjanovic Ana  Dobricic Valerija S Brankovic Marija  Jankovic Milena Z  Mandic Gorana B Stefanova Elka D  Stevic Zorica D Novakovic Ivana V  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 961-961
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov NOTCH3 mutations in Serbian CADASIL patients (Meeting Abstract)
Autori Jankovic Milena Z  Dobricic Valerija S Marjanovic Ana  Brankovic Marija  Pavlovic Aleksandra M  Dujmovic Irena Mijajlovic Milija D  Novakovic Ivana V  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 293-293
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Use of clinical exome analysis in rare neurodegenerative disorders in Serbian population: Firs experience (Meeting Abstract)
Autori Brankovic M Dobricic Valerija S Svetel Marina V  Peric Stojan Z  Stefanova Elka D  Marjanovic Ana  Petrovic Igor N Novakovic Ivana V  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 292-292
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients (Meeting Abstract)
Autori Mitropoulos Konstantinos ... Dobricic Valerija S Novakovic Ivana V  Kostic Vladimir S ... (broj koautora 33) 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 252-253
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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