Researchers
Novaković, Ivana
Results 121-140 of 395
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2019 | Significance of KIT and PDGFRA mutations in gastric gastrointestinal stromal tumor imatinib-naive surgically treated patients![]() | Ebrahimi, Keramatollah | Article | 23M23 |
| 2019 | Genetika amiotrofične lateralne skleroze![]() | Stević, Zorica | Conference Paper | Mp. category will be shown later |
| 2019 | Associations of Common Variants in HFE and TMPRSS6 Genes with Hepcidin-25 and Iron Status Parameters in Patients with End-Stage Renal Disease![]() | Dopsaj, Violeta | Article | 21M21 |
| 2019 | Polymorphisms in PPARG gene: association with obesity-related metabolic traits in a Serbian adolescent population![]() | Pešić, Milica | Conference Paper | Mp. category will be shown later |
| 2019 | Results of clinical exome analysis in rare neurodegenerative disorders in Serbian population![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2019 | KRIT1 Gene Analysis In Serbian Patients With Familial Cerebral Cavernous Malformation![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2019 | Analysis of endothelial nitric oxide synthase T786C gene polymorphism in surgical patients with diffuse secondary peritonitis![]() | Gulić, Milica N. | Conference Paper | Mp. category will be shown later |
| 2019 | Analysis of the association between ITPA rs1127354 gene polymorphism and efficacy and toxicity of methotrexate in patients with rheumatoid arthritis![]() | Grk, Milka | Conference Paper | Mp. category will be shown later |
| 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 | 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 | Patofiziologija - mehanizmi poremećaja zdravlja - Deo 1.![]() | Čemerikić, Dušan; De Luka, Silvio | Text book | Mp. category will be shown later |
| 2019 | The frequency of C9orf72 repeat expansion beyond ALS/FTD spectrum in Serbian patients with neurodegenerative disorders![]() | Marjanović, Ana | 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 | 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 |
| 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 | GLUT1 deficiency syndrome : a case report with a novel SLC2A1mutation![]() | Ivančević, Nikola | Article | 23M23 |
| 2019 | Angiogenin gene mutations in patients with amyotrophic lateral sclerosis from tertiary center in Belgrade![]() | Janković, Milena | 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 | 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 |
