Autori: Marjanovic Ana
| Naslov | Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1 ss, andTNF-alpha in relation with Parkinson's disease progression (Meeting Abstract) |
| Autori | Pesic Milica Maksimovic Nela S Aleksic Andjelka Gulic Milica Djuranovic Ana S Grk Milka B Dusanovic-Pjevic Marija G Stankovic Iva D Markovic Vladana V Marjanovic Ana Novakovic Ivana V Dragasevic-Miskovic Natasa T Kostic Vladimir S |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 888-888 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy (Article) |
| Autori | Dawod Phepy GA Jancic Jasna B Marjanovic Ana Marjanovic Ana Jankovic Milena Z Samardzic Janko M Potkonjak Dario Djuric Vesna Mesaros Sarlota T Novakovic Ivana V Abdel Motaleb Fayda I Kostic Vladimir S Nikolic Dejan P |
| Info | GENES, (2020), vol. 11 br. 9, str. - |
| Projekat | Serbian Ministry of Education, Science and Technological Development [ON175090, ON175091, 200110] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | The influence of ANNK1/DRD2 haplotypes on the onset of complications of long-term levodopa therapy in Parkinson's disease (Meeting Abstract) |
| Autori | Radojevic Branislava Dragasevic-Miskovic Natasa T Marjanovic Ana Milovanovic Andona Svetel Marina V Petrovic Igor N Savic Miroslav M Jancic Ivan R Kostic Vladimir K |
| Info | MOVEMENT DISORDERS, (2020), vol. 35 br. , Suppl. 1, str. S473-S474 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Yield of thePMP22deletion analysis in patients with compression neuropathies (Article) |
| Autori | Ivanovic Vukan Marjanovic Ana Bjelica Bogdan Kacar Aleksandra S Tubic Radoje M Jankovic Milena Z Marjanovic Ana Novakovic Ivana V Rakocevic-Stojanovic Vidosava M Peric Stojan Z |
| Info | JOURNAL OF NEUROLOGY, (2020), vol. 267 br. 12, str. 3617-3623 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Neuropathic pain in patients with Charcot-Marie-Tooth type 1A (Article) |
| Autori | Bjelica Bogdan Peric Stojan Z Basta Ivana Z Bozovic Ivo Kacar Aleksandra S Marjanovic Ana Ivanovic Vukan Marjanovic Ana Jankovic Milena Z Novakovic Ivana V Rakocevic-Stojanovic Vidosava M |
| Info | NEUROLOGICAL SCIENCES, (2020), vol. 41 br. 3, str. 625-630 |
| Projekat | Ministarstvo Prosvete, Nauke i Tehnoloskog Razvoja [175083] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| 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 | 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 | 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 | 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 |
