Autori: Dobricic Valerija S
| Naslov | The pattern of inheritance and genetic status in early onset Alzheimer's disease and frontotemporal dementia (Meeting Abstract) |
| Autori | Mandic-Stojmenovic Gorana B Stefanova Elka D  Novakovic Ivana V Dobricic Valerija S Stojkovic Tanja Kostic Vladimir K
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| Info | EUROPEAN JOURNAL OF NEUROLOGY, (2019), vol. 26 br. , Suppl. 1, str. 120-120 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease (Meeting Abstract) |
| Autori | Jankovic Milena Z Dobricic Valerija S Kresojevic Nikola D Markovic Vladana V Petrovic Igor N Svetel Marina V Pekmezovic Tatjana D Novakovic Ivana V Kostic Vladimir K
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| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 410-411 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders (Meeting Abstract) |
| Autori | Marjanovic Ana Dobricic Valerija S Marjanovic Ivan V Brankovic Marija Jankovic Milena Z Mandic Gorana B Stevic Zorica D Novakovic Ivana V Stefanova Elka D Kostic Vladimir K
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| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 376-376 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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| Naslov | Contribution to the knowledge on the distribution of freshwater sponges - the Danube and Sava rivers case study (Article) |
| Autori | Andjus Stefan P Nikolic Nadja S Dobricic Valerija S Marjanovic Ana Gacic Zoran M Brankovic Goran O Akovic Maja R Paunovic Momir M
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| Info | JOURNAL OF LIMNOLOGY, (2018), vol. 77 br. 2, str. 199-208 |
| Projekat | Ministry of Education, Science and Technological Development of the Republic of Serbia [176018]; European Union [603629-ENV-2013-6.2.1-GLOBAQUA]; European Commission |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease (Article) |
| Autori | Jankovic Milena Z Dobricic Valerija S Kresojevic Nikola D Markovic Vladana V Petrovic Igor N Svetel Marina V Pekmezovic Tatjana D Novakovic Ivana V Kostic Vladimir K
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| Info | JOURNAL OF THE NEUROLOGICAL SCIENCES, (2018), vol. 393 br. , str. 27-30 |
| Projekat | Serbian Ministry of Science and Technological Development [ON175090, ON175091] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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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 30)
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| Info | PUBLIC HEALTH GENOMICS, (2018), vol. 21 br. , Suppl. 1, str. 17-17 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
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| 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
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| 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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| 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
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| 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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients (Article) |
| Autori | Mitropoulos Konstantinos ... Dobricic Valerija S Novakovic Ivana V Kostic Vladimir S ... (broj koautora 33)
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| Info | HUMAN GENOMICS, (2017), vol. 11 br. , str. - |
| Projekat | European Commission [RD-Connect] [FP7-305444]; European Commission [U-PGx] [H2020-668353]; Greek General Secretariat of Research and Technology [eMoDiA] [PiDeltaE11_0415]; Golden Helix Foundation; Serbian Ministry of Education, Science and Technology deve |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans (Article) |
| Autori | Lohmann Katja ... Dobricic Valerija S ... Savic-Pavicevic Dusanka Lj ... (broj koautora 18)
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| Info | HUMAN MOLECULAR GENETICS, (2017), vol. 26 br. 6, str. 1078-1086 |
| Projekat | NIH [NS081282, HL105550]; German Ministry of Education and Research (BMBF, DYSTRACT consortium) [01GM1514B]; Ministry of Education, Science and Technological Development, Republic of Serbia [173016, 175090]; Hermann and Lilly Schilling Foundation |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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