Researchers
Novaković, Ivana
Results 141-160 of 392
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2019 | Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy![]() | Dawod, Phepy G. A.; Rovčanin, Branislav R.; Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2019 | Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients![]() | Mitropoulos, Konstantinos; ...; Dobričić, Valerija S. | Conference Paper | Mp. category will be shown later |
| 2019 | Association between Tumor Necrosis Factor-alpha Promoter-308 G/A Polymorphism and Early Onset Sepsis in Preterm Infants![]() | Varljen, Tatjana; Rakić, Olgica; Sekulović, Gordana; Jekić, Biljana | Article | 22M22 |
| 2019 | Genetic variant rs16944 in IL1B gene is a risk factor for early onset sepsis susceptibility and outcome in preterm infants![]() | Maksimović, Nela S. | Conference Paper | Mp. category will be shown later |
| 2019 | Genetika amiotrofične lateralne skleroze![]() | Stević, Zorica | Conference Paper | Mp. category will be shown later |
| 2019 | Association of C35T polymorphism in dihydrofolate reductase gene with toxicity of methotrexate in rheumatoid arthritis patients![]() | Vejnović, Dubravka | Article | 21M21 |
| 2019 | Significance of KIT and PDGFRA mutations in gastric gastrointestinal stromal tumor imatinib-naive surgically treated patients![]() | Ebrahimi, Keramatollah | Article | 23M23 |
| 2019 | Spectrum of mutations in presenilin 1 gene in patients with early onset Alzheimer disease![]() | Andabaka, Marko | Conference Paper | Mp. category will be shown later |
| 2019 | Clinical course of patients with pantothenate kinase-associated neurodegeneration (PKAN) before and after DBS surgery![]() | Svetel, Marina | Article | 21M21 |
| 2019 | The pattern of inheritance and genetic status in early onset Alzheimer's disease and frontotemporal dementia![]() | Mandić-Stojmenović, Gorana B. | Conference Paper | Mp. category will be shown later |
| 2019 | Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes![]() | Vidmar, Lovro; Maver, Ales; Drulović, Jelena | Article | 21M21 |
| 2019 | Polymorphisms in PPARG gene: Association with obesity-related metabolic traits in Serbian adolescent population![]() | Pešić, Milica M. | Conference Paper | Mp. category will be shown later |
| 2019 | Molecular genetic testing of Huntington’s disease and genetic counselling![]() | Mandić, Ratka; Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2019 | Association of genetic markers of coagulation and fibrinolysis with prematurity complication![]() | Damnjanović, Tatjana M. | Conference Paper | Mp. category will be shown later |
| 2019 | Genetski zasnovana terapija neurodegenerativnih bolesti![]() | Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2018 | NPC1 and NPC2 gene analysis in Serbian patients with Niemann-Pick disease type C![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2018 | Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease![]() | Janković, Milena Z. | Conference Paper | Mp. category will be shown later |
| 2018 | Humana genetika : sveska za praktične radove![]() | Luković, Ljiljana | Text book | Mp. category will be shown later |
| 2018 | Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion![]() | Hodžić, Alenka; Lavtar, Polona; Ristanović, Momčilo | Article | 21M21 |
| 2018 | Study of the polymorphisms in genes IL-17, IL-23, TGFb, RORgT and FOXP3 in Serbian patients with antiphospholipid syndrome![]() | Novaković, Ivana V. | Conference Paper | Mp. category will be shown later |
