Researchers
Novaković, Ivana
Results 41-60 of 394
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2024 | ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series![]() | Milovanović, Andona | Article | 21a+M21a+ |
| 2024 | C9orf72 genetic screening in patients with ALS/FTD phenotype from Serbia![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2024 | Wilson’s disease![]() | Svetel, Marina | Article | 23M23 |
| 2024 | Етички аспекти генетског тестирања![]() | Новаковић, Ивана | Conference Paper | Mp. category will be shown later |
| 2024 | Adrenal hypoplasia congenita and hypogonadotropic hypogonadism due to a novel NR0B1 (DAX1) gene mutation associated with common variable immunodeficiency and Hashimoto's thyroiditis![]() | Ćirić, Jasmina D. | Article | 22M22 |
| 2024 | Challenges in rare diseases: The example of mitochondrial diseases![]() | Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2024 | Physical activity and mental health of medical students![]() | Stratakis, Konstantinos; Terzić-Šupić, Zorica | Article | 23M23 |
| 2024 | Rare and Uncommon Gene Variants Associated with Familial Multiple Sclerosis: A Case-Control Study![]() | Jovanović, Aleksa | Conference Paper | Mp. category will be shown later |
| 2024 | Exclusive breastfeeding may be a protective factor in individuals with familial multiple sclerosis. A population registry-based case-control study![]() | Jovanović, Aleksa Lj. | Article | 21M21 |
| 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 | LGALS3 RS4644 gene polymorphism is associated with obesity related metabolic traits in Serbian adolescent population![]() | Damnjanović, Tatjana | Conference Paper | Mp. category will be shown later |
| 2023 | The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti![]() | Minić, Snežana B. | Article | 21M21 |
| 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 |
| 2023 | Analysis of clinical exome panel in rare neurodegenerative disorders in Serbian population![]() | Branković, Marija | 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 | Clinical phenotype of amyotrophic lateral sclerosis with C9ORF72 repeat expansion in Serbia![]() | Virić, Vanja | Conference Paper | Mp. category will be shown later |
| 2023 | C9orf72 genetic screening in amyotrophic lateral sclerosis patients from Serbia![]() | Marjanović, Ana | Article | 22M22 |
| 2023 | miRNAs as a Potential Biomarker in the COVID-19 Infection and Complications Course, Severity, and Outcome![]() | Janković, Milena | Article | 21M21 |
