Istraživači
Novaković, Ivana
Results 81-100 of 394
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2022 | Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the Balkans![]() | Maver, Aleš; Kovanda, Anja; Bergant, Gaber; Teran, Nataša; Vrečar, Irena; Branković, Marija
Rački, Valentino; Vuletić, Vladimira; Peterlin, Borut;
| Conference Paper | Mp. category will be shown later |
| 2022 | Correlation between leukocyte-platelet aggregates and thrombosis in myeloproliferative neoplasms![]() | Šefer, Dijana | Article | 22M22 |
| 2022 | A multicenter study of genetic testing for Parkinson’s disease in the clinical setting![]() | Kovanda, Anja; Rački, Valentino; Bergant, Gaber; Georgiev, Dejan; Flisar, Dušan; Papić, Eliša; Branković, Marija | Article | 21aM21a |
| 2022 | PPARGC1A gene polymorphism and its association with obesity-related metabolic traits in Serbian adolescent population![]() | Vidović, Vanja; Maksimović, Nela S. | Article | 22M22 |
| 2022 | KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizure![]() | Dimitrijević, Sanja; Jekić, Biljana | Article | 21M21 |
| 2021 | Association of PPARG rs3856806 C>T polymorphism with body mass index, glycaemia and lipid parameters in Serbian adolescents![]() | Vidović, Vanja; Maksimović, Nela | Article | Mp. category will be shown later |
| 2021 | Genetic variants in TNFA, LTA, TLR2 and TLR4 genes and risk of sepsis in patients with severe trauma: nested case-control study in a level-1 trauma centre in SERBIA![]() | Đurić, Olivera | Article | 21M21 |
| 2021 | The FKBP5 genotype and childhood trauma effects on FKBP5 DNA methylation in patients with psychosis, their unaffected siblings, and healthy controls![]() | Mihaljević, Marina | Article | 21aM21a |
| 2021 | Clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2021 | Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review![]() | Dawod, Phepy; Jančić, Jasna | Article | 21M21 |
| 2021 | Genetic and epigenomic modifiers of diabetic neuropathy![]() | Janković, Milena | Article | 21M21 |
| 2021 | NBIA Syndromes: A Step Forward from the Previous Knowledge![]() | Svetel, Marina V. | Article | 23M23 |
| 2021 | Premutations in the FMR1 gene in Serbian patients with undetermined tremor, ataxia and parkinsonism![]() | Pešić, Milica | Article | 22M22 |
| 2021 | Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis![]() | Janković, Milena | Article | 21M21 |
| 2021 | Phenotype characteristics of ANO10 mutation carries: a case series from Serbia and a systematic review of the literature![]() | Stanković, Iva | Conference Paper | Mp. category will be shown later |
| 2021 | Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents![]() | Maksimović, Nela | Article | 21aM21a |
| 2020 | Novel PANK2 mutation identified in a patient with pantothenate kinase-associated neurodegeneration![]() | Svetel, Marina V. | Article | 23M23 |
| 2020 | Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic Neuropathy![]() | Dawod, Phepy G. A.; Jančić, Jasna | Article | 21M21 |
| 2020 | Yield of the PMP22 deletion analysis in patients with compression neuropathies![]() | Ivanović, Vukan | Article | 21M21 |
| 2020 | Neurologija : za studente medicine![]() | Kostić, Vladimir
Kozić, Duško
| Text book | Mp. category will be shown later |
