Istraživači
Novaković, Ivana
Godina
- 68 2020 - 2025
- 214 2010 - 2019
- 62 2000 - 2009
- 3 1990 - 1999
Mp-kat.
- 2 M53
- 1 M51
- 1 M70
- < Prethodan
Godina - raspon
Godina | Naslov | Autor(i) | Tip rezultata | Mp-kat. |
---|---|---|---|---|
2019 | Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy (✓) | Dawod, Phepy G. A.; Rovčanin, Branislav R.; Branković, Marija ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2019 | GLUT1 deficiency syndrome : a case report with a novel SLC2A1mutation (✓) | Ivančević, Nikola ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Naučni članak | 23M23 - Rad u međ. časopisu |
2019 | The frequency of C9orf72 repeat expansion beyond ALS/FTD spectrum in Serbian patients with neurodegenerative disorders (✓) | Marjanović, Ana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2019 | Genetic variant rs16944 in IL1B gene is a risk factor for early onset sepsis susceptibility and outcome in preterm infants | Maksimović, Nela S. ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2019 | Association between tumor necrosis factor-α promoter -308 g/a polymorphism and early onset sepsis in preterm infants (✓) | Varljen, Tatjana; Rakić, Olgica; Sekulović, Gordana; Jekić, Biljana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Naučni članak | 22M22 - Rad u istaknutom međ. časopisu |
2019 | Patofiziologija - mehanizmi poremećaja zdravlja - Deo 1. (✓) | Čemerikić, Dušan; De Luka, Silvio ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Udžbenik | Mp kategorija će biti prikazana naknadno. |
2019 | phenotypic and genetic heterogeneity of adult patients with hereditary spastic paraplegia from Serbia | Peric, Stojan Z ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2019 | Use of clinical exome analysis in rare neurodegenerative disorders in Serbian population: First experience (✓) | Branković, Marija ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2018 | Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease (✓) | Janković, Milena ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Naučni članak | 22M22 - Rad u istaknutom međ. časopisu |
2018 | Humana genetika : sveska za praktične radove (✓) | Luković, Ljiljana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Monografija | Mp kategorija će biti prikazana naknadno. |
2018 | Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion (✓) | Hodžić, Alenka; Lavtar, Polona; Ristanović, Momčilo ![]() ![]() ![]() ![]() ![]() ![]() | Naučni članak | 21M21 - Rad u vrhunskom međ. časopisu |
2018 | NPC1 and NPC2 gene analysis in Serbian patients with Niemann-Pick disease type C | Brankovic, M; Kresojevic, Nikola D ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2018 | Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease | Jankovic, Milena Z ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2018 | Humana genetika - sveska za praktične radove | Luković, Ljiljana; Novaković, Ivana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Udžbenik | |
2018 | Neurologija : za studente medicine | Kostić, Vladimir ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]()
Kozić, Duško
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Udžbenik | Mp kategorija će biti prikazana naknadno. |
2018 | Analysis of pathogenic mtDNA mutations associated with Leber's hereditary optic neuropathy: our experience (✓) | Dawod, Phepy Gamil Anwar; Rovčanin, Branislav ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2018 | The burden of rare genetic variants in genes involved in tumor necrosis factor (TNF) signalling pathway in multiple sclerosis (MS) | Peterlin, AM; Maver, Ales; Hodzic, A; Sega, S; Drulovic, Jelena S ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2018 | Genomic Variants in the FTO Gene are Associated with Sporadic Amyotrophic Lateral Sclerosis in Greek Patients | Mitropoulos, Konstantinos; ...; Dobricic, Valerija S; Novakovic, Ivana V ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2018 | C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders | Marjanovic, Ana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
2018 | Study of the polymorphisms in genes IL-17, IL-23, TGFb, RORgT and FOXP3 in Serbian patients with antiphospholipid syndrome | Novakovic, Ivana V ![]() ![]() ![]() ![]() | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |