Autori: Novakovic Ivana V
| Naslov | GLUT1 deficiency syndrome: a case report with a novel SLC2A1 mutation (Article) |
| Autori | Ivancevic Nikola Cerovac Natasa M Nikolic Blazo Cuturilo Goran Marjanovic Ana Marjanovic Ana Novakovic Ivana V |
| Info | VOJNOSANITETSKI PREGLED, (2019), vol. 76 br. 5, str. 543-546 |
| Projekat | Serbian Ministry of Education, Science and Technological Development [ON175091] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Clinical course of patients with pantothenate kinase-associated neurodegeneration (PKAN) before and after DBS surgery (Article) |
| Autori | Svetel Marina V Tomic Aleksandra D Dragasevic Natasa T Petrovic Igor N Kresojevic Nikola D Jech Robert Urgosik Dusan Banjac Isidora Vitkovic Jelena Novakovic Ivana V Kostic Vladimir S |
| Info | JOURNAL OF NEUROLOGY, (2019), vol. 266 br. 12, str. 2962-2969 |
| Projekat | Ministry of Education, Science and Technological Development of the Republic of Serbia [175090] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy (Meeting Abstract) |
| Autori | Dawod Phepy GA Rovcanin Branislav R Marjanovic Ana Marjanovic Ana Jankovic Milena Z Novakovic Ivana V Motaleb Abdel F Jancic Jasna B Kostic Vladimir S |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1836-1837 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Genetic variant rs16944 in IL1B gene is a risk factor for early onset sepsis susceptibility and outcome in preterm infants (Meeting Abstract) |
| Autori | Maksimovic Nela S Varljen Tatjana J Sekulovic Gordana Damnjanovic Tatjana M Novakovic Ivana V |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1364-1365 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Study of TNF, IL1B, and IL6 genes polymorphisms and susceptibility to bronchopulmonary dysplasia in premature neonates (Meeting Abstract) |
| Autori | Damnjanovic Tatjana M Varljen Tatjana J Rakic Olgica Jekic Biljana B Liston J Novakovic Ivana V |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1360-1360 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| 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 | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Association of PRDM16 and CtBP2 genes polymorphisms with lipid profile of adolescents (Meeting Abstract) |
| Autori | Maksimovic Nela S Vidovic Vanja Damnjanovic Tatjana M Jekic Biljana B Perovic Dijana Vidovic Stojko Milovac Irina Novakovic Ivana V |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 658-658 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Association of genetic markers of coagulation and fibrinolysis with prematurity complication (Meeting Abstract) |
| Autori | Damnjanovic Tatjana M Grk Milka B Varljen Tatjana J Pantelic Jelica R Maksimovic Nela S Jekic Biljana B Novakovic Ivana V |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 641-642 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| 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 | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| 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 | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
