Researchers
Novaković, Ivana
Results 41-60 of 383
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2023 | Yield of GATOR1 gene sequencing in a Serbian focal epilepsy cohort![]() | Kovačević, Maša | Conference Paper | Mp. category will be shown later |
| 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 | 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 | Novel variants in established epilepsy genes in focal epilepsy![]() | Kovačević, Maša | Article | 22M22 |
| 2023 | C9ORF72 intermediate repats in neurodegenerative disorders from Serbia![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2023 | Novel GATOR1 variants in focal epilepsy![]() | Kovačević, Maša | Article | 22M22 |
| 2023 | The importance of direct genetic testing to determine female carriers in dystrophinopathies![]() | Maksić, Jasmina | Article | 23M23 |
| 2023 | The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti![]() | Minić, Snežana B. | Article | 21M21 |
| 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 | miRNAs as a Potential Biomarker in the COVID-19 Infection and Complications Course, Severity, and Outcome![]() | Janković, Milena | Article | 21M21 |
| 2023 | Clinical and genetic features of Huntington’s disease patients from Serbia: A single-center experience![]() | Kresojević, Nikola | Article | 21M21 |
| 2023 | Motor neuron involvement in facial muscles as characteristic of ANO10 mutation![]() | Dragašević-Mišović, Nataša | Conference Paper | Mp. category will be shown later |
| 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 | Reply to: “Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism”![]() | Kresojević, Nikola | Article | 21a+M21a+ |
| 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 |
| 2022 | Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia![]() | Perić, Stojan | 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 |
