Autori: Novakovic Ivana V
| Naslov | Study of the polymorphisms in genes IL-17, IL-23, TGFb, RORgT and FOXP3 in Serbian patients with antiphospholipid syndrome (Meeting Abstract) |
| Autori | Novakovic Ivana V Popovic-Kuzmanovic Dragana Stojanovic Ljudmila Trajkovic Vladimir S |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 906-906 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| 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 |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 410-411 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | NPC1 and NPC2 gene analysis in Serbian patients with Niemann-Pick disease type C (Meeting Abstract) |
| Autori | Brankovic Marija Kresojevic Nikola D Marjanovic Ana Novakovic Ivana V Kostic Vladimir K |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 406-406 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | The burden of rare genetic variants in genes involved in tumor necrosis factor (TNF) signalling pathway in multiple sclerosis (MS) (Meeting Abstract) |
| Autori | Peterlin AM Maver Ales Hodzic A Sega Sasa Drulovic Jelena S Novakovic Ivana V Pekmezovic Tatjana D Ristic S Kapovic Miljenko Peterlin Borut |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 400-400 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| 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 |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 376-376 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| 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 |
| Info | JOURNAL OF THE NEUROLOGICAL SCIENCES, (2018), vol. 393 br. , str. 27-30 |
| Projekat | Serbian Ministry of Science and Technological Development [ON175090, ON175091] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| 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) |
| Info | PUBLIC HEALTH GENOMICS, (2018), vol. 21 br. , Suppl. 1, str. 17-17 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion (Article) |
| Autori | Hodzic Alenka Lavtar Polona Ristanovic Momcilo Novakovic Ivana V Dotlic Jelena R Peterlin Borut |
| Info | PLOS ONE, (2018), vol. 13 br. 5, str. - |
| Projekat | Slovenian Research Agency [P3-0326] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Association of Fetuin Gene Polymorphisms with Coronary Artery Calcifications and Mortality in Renal Transplant and Chronic Kidney Disease Patients (Meeting Abstract) |
| Autori | Jovicic-Pavlovic Svetlana M Simic-Ogrizovic Sanja P Dopsaj Violeta Novakovic Ivana V Bukumiric Zoran M Naumovic Radomir T |
| Info | NEPHROLOGY DIALYSIS TRANSPLANTATION, (2017), vol. 32 br. , Suppl. 3, str. 733-733 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| 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 |
