Researchers
Novaković, Ivana
Results 141-160 of 394
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2019 | Correlation of selected polymorphisms in COMT, DAT (SL6A3), DRD2, and ANKK1 genes and complications of long-term levodopa treatment in patients with idiopathic Parkinsons disease![]() | Radojević, Branislava | Conference Paper | Mp. category will be shown later |
| 2019 | Association of PRDM16 and CtBP2 genes polymorphisms with lipid profile of adolescents![]() | Maksimović, Nela S. | Conference Paper | Mp. category will be shown later |
| 2019 | Analysis of the Association Between Polymorphisms within PAI-1 and ACE genes and Ischemic Stroke Outcome After rt-PA Therapy![]() | Dušanović-Pjević, Marija G. | Article | 22M22 |
| 2019 | Increased burden of ultra-rare genetic variants in the inflammasome regulatory genes in patients with multiple sclerosis![]() | Peterlin, Borut; Vidmar, Lovro; Drulović, Jelena S. | Conference Paper | Mp. category will be shown later |
| 2019 | NOTCH3 mutations in Serbian CADASIL patients![]() | Janković, Milena Z. | Conference Paper | Mp. category will be shown later |
| 2019 | The efects of ApoB Thr71Ile and ApoE 112/158 gene polymorphisms on parameters of lipid metabolism in the serbian overweight and obese adolescents![]() | Đuranović, Ana | Conference Paper | Mp. category will be shown later |
| 2019 | Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2019 | Analisys of the association of TNFα, IL1 β and IL6 promotor gene polymorphisms with the development of severe form of retinopathy of prematurity![]() | Ćućuz, Milica; Pantelić, Jelica; Varljen, Tatjana; Grk, Milka | 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 | 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 | 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 | 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 | 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 | Analysis of the association of TNFΑ, IL1Β and IL6 promotor gene polymorphisms with the development of severe form of retinopathy of prematurity![]() | Ćućuz, Milica; Pantelić, Jelica; Varljen, Tatjana; Grk, Milka | Conference Paper | Mp. category will be shown later |
| 2019 | Study of TNF, IL1B, and IL6 genes polymorphisms and susceptibility to bronchopulmonary dysplasia in premature neonates![]() | Damnjanović, Tatjana M. | Conference Paper | Mp. category will be shown later |
| 2019 | Phenotypic and genetic heterogeneity of adult patients with hereditary spastic paraplegia from Serbia![]() | Perić, Stojan Z. | Conference Paper | Mp. category will be shown later |
| 2018 | Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease![]() | Janković, Milena | Article | 22M22 |
| 2018 | 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 |
| 2018 | Analysis of pathogenic mtDNA mutations associated with Leber's hereditary optic neuropathy: our experience![]() | Dawod, Phepy Gamil Anwar; Rovčanin, Branislav | Conference Paper | Mp. category will be shown later |
