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Browsing by Author Klaassen, Kristel M
Showing results 1 to 5 of 5
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2025 | Applications of the new tool: VUS Notifier | Domazet, Milan; Ugrin, Milena M; Andjelkovic, Marina Z; Klaassen, Kristel M; Skakic, Anita G   ; Komazec, Jovana; Spasovski, Vesna M ; Todorovic, Sasa; Stojiljkovic, Maja M | Conference Paper | Mp. category will be shown later |
| 2025 | Integration of federated learning to study of pathologies with intellectual disabilities within the European BETTER Consortium | Barco-Armengol, Nidia; ...; Stojiljkovic, Maja M; Klaassen, Kristel M; Stankovic, Sara S; Komazec, Jovana; ...; (broj, koautora 19) | Conference Paper | Mp. category will be shown later |
| 2025 | Thalassemia syndromes in Serbia:the importance of genetic (re)analysis | Ugrin, Milena M; Komazec, Jovana; Klaassen, Kristel M; Skakic, Anita G ; Andjelkovic, Marina Z; Spasovski, Vesna M ; Stevanovic, Nina ; Parezanovic, Marina V; Stankovic, Sara S; Jocic, Nikola;
Pavlovic, Sonja T; Stojiljkovic, Maja M;
| Conference Paper | Mp. category will be shown later |
| 2025 | Unravelling phenylalanine-induced neuronal dysfunction: transcriptome analysis of NT2-derived neurons highlights neurite impairment and synaptic connectivity | Stankovic, Sara; Lazic, Andrijana ; Parezanovic, Marina V; Andjelkovic, Marina Z; Ugrin, Milena M; Stevanovic, Milena J ; Pavlovic, Sonja T; Stojiljkovic, Maja M; Klaassen, Kristel M | Conference Paper | Mp. category will be shown later |
| 2026 | Behçet's syndrome-like features revealing myelodysplastic syndrome with TP53 mutation: a case report | Pesic, Andrej; Ljubicic, Jelena; Todorovic-Balint, Milena; Klaassen, Kristel M; Andjelkovic, Marina Z; Pavlovic, Sonja T; Stojanovic, Maja | Article | 21M21 |