Researchers
Novaković, Ivana
Results 61-80 of 394
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | TREM2 R47H as a risk factor for Alzheimer's disease in Serbian patients![]() | Pešić, Milica | Conference Paper | Mp. category will be shown later |
| 2023 | The association of R47H variant in the TREM2 gene and genetic susceptibility to Alzheimer's disease in Serbian population![]() | Andrejić, Nikola; Pešić, Milica | Article | 53M53 |
| 2023 | C9orf72 genetic screening in amyotrophic lateral sclerosis patients from Serbia![]() | Marjanović, Ana | Article | 22M22 |
| 2023 | Clinical phenotype of amyotrophic lateral sclerosis with C9ORF72 repeat expansion in Serbia![]() | Virić, Vanja | Conference Paper | Mp. category will be shown later |
| 2023 | Genetic Testing in Parkinson's Disease![]() | Pal, Gian; ...; Novakovicć, Ivana V. | Article | 21a+M21a+ |
| 2023 | Yield of GATOR1 gene sequencing in a Serbian focal epilepsy cohort![]() | Kovačević, Maša | Conference Paper | Mp. category will be shown later |
| 2023 | EPR-210 Whole exome sequencing in Serbian patients with hereditary spastic paraplegia![]() | Ivanović, Vukan | Conference Paper | Mp. category will be shown later |
| 2023 | Analysis of clinical exome panel in rare neurodegenerative disorders in Serbian population![]() | Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2023 | International Genetic Testing and Counseling Practices for Parkinson's Disease![]() | Saunders-Pullman, Rachel; ...; Novaković, Ivana V. | Article | 21a+M21a+ |
| 2023 | CYP2C9 screening: important step in siponimod treatment of secondary progressive multiple sclerosis![]() | Janković, Milena | Conference Paper | Mp. category will be shown later |
| 2022 | Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous GBA Mutation![]() | Minić, Snežana B. | Article | 21M21 |
| 2022 | KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizure![]() | Dimitrijević, Sanja; Jekić, Biljana | Article | 21M21 |
| 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 | Correlation between leukocyte-platelet aggregates and thrombosis in myeloproliferative neoplasms![]() | Šefer, Dijana | Article | 22M22 |
| 2022 | Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients![]() | Perović, Dijana | Article | 22M22 |
| 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 | Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages![]() | Pereza, Nina; Terzic, Rifet; Plaseska-Karanfilska, Dijana; Miljanovic, Olivera; Novaković, Ivana V. | Article | 21M21 |
| 2022 | The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options![]() | Janković, Milena | Article | 21M21 |
| 2022 | C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population![]() | Marjanović, Ana | Article | 22M22 |
