Researchers
Klaassen Ljubičić, Kristel
Results 1-20 of 100
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2026 | Behçet's syndrome-like features revealing myelodysplastic syndrome with TP53 mutation: a case report![]() | Pešić, Andrej; Ljubičić, Jelena | Article | 21M21 |
| 2026 | Ispitivanje patofiziologije i terapijskih strategija za glikogenozu tip Ib upotrebom CRISPR/Cas9 i iPSC model sistema | Petrović, Isidora; Parezanović, Marina | Conference Paper | Mp. category will be shown later |
| 2026 | Phenylketonuria: Importance of neonatal screening, insights into genotype-phenotype correlations, and novel therapeutic approaches![]() | Đorđević, Milošević | Article | Mp. category will be shown later |
| 2026 | First Reported Use of Recombinant Parathyroid Hormonein Kenny–Caffey Syndrome Type 2: A Case Report andLiterature Review![]() | Milošević Đorđević, Maja; Skakić, Anita | Article | 22M22 |
| 2026 | RHOBTB2-Associated Neurological Phenotypes and Underlying Mechanisms: Alternating Hemiplegia of Childhood Beyond ATP1A3 | Kravljanac, Ruzica M; Klaassen, Kristel M | Reviews | 22M22 |
| 2026 | Neuromuscular Disorders in Children Through the Lens of Next-Generation Sequencing: A Study of Diagnostic Yield![]() | Ostojić, Slavica; Kovačević, Gordana | Article | 21M21 |
| 2026 | Pregled metaboličkih retkih bolesti detektovanih u Srbiji radi odabira najpogodnijih bolesti za pravljenje novog hepatičnog modela bolesti baziranog na iPSC | Grujić, Kristina | Conference Paper | Mp. category will be shown later |
| 2026 | Uticaj tretmana mikroRNK-34 familije na ciliogenezu u NHBE in vitro modelu humanog respiratornog epitela | Petrović, Isidora; Stevanović, Nina | Conference Paper | Mp. category will be shown later |
| 2026 | Sekvenciranje kompletnog genoma dugim očitavanjima (LR-WGS) u cilju preciznije molekularno-genetičke dijagnoze kongenitalne adrenalne hiperplazije | Petrović, Isidora; Jocić, Nikola | Conference Paper | Mp. category will be shown later |
| 2025 | Applications of the new tool: VUS Notifier![]() | Domazet, Milan; Ugrin, Milena 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 | Conference Paper | Mp. category will be shown later |
| 2025 | Thalassemia syndromes in Serbia:the importance of genetic (re)analysis![]() | Ugrin, Milena | Conference Paper | Mp. category will be shown later |
| 2025 | Multiphasic acute disseminated encephalomyelitis (MDEM) in a patient with systemic lupus erythematosus and C4A deficiency: case-based review![]() | Ljubičić, Jelena | Article | 21M21 |
| 2025 | MITOCHONDRIAL MYOPATHY CAUSED BY MT-ND5 VARIANT: INTEGRATING WES AND MITOCHONDRIAL DNA ANALYSIS | Klaassen, Kristel | Conference Paper | Mp. category will be shown later |
| 2025 | Heterologous expression of human glucose-6-phosphate translocase (SLC37A4) in prokaryotic and yeast systems | Stanišić, Marija; Ugrin, Milena | Conference Paper | Mp. category will be shown later |
| 2025 | Advancing the IMGGE RD Biobank through BRIDGING-RD Project: Achieving full interoperability of genetic and phenotypic data to enhance participation in transnational research and innovation for human health | Komazec, Jovana | Conference Paper | Mp. category will be shown later |
| 2025 | ESTABLISHING IN VITRO MODELS FOR GLYCOGEN STORAGE DISEASE TYPE IB: A PLATFORM FOR THERAPEUTIC INVESTIGATIONS![]() | Jocić, Nikola | Conference Paper | Mp. category will be shown later |
| 2025 | Establishment of an insulin resistance model in HepG2 cells using combined high glucose and insulin treatment | Spasovski, Vesna | Conference Paper | Mp. category will be shown later |
| 2025 | CRISPR/Cas9 and iPSC-based platforms to explore pathophysiology and therapeutic approaches in glycogen storage disease type Ib | Skakić, Anita | Conference Paper | Mp. category will be shown later |
| 2025 | Genomic profiling, implications for genotype-based treatment of 131 patients with phenylketonuria and characterization of novel p.Pro416Leu PAH variant | Klaassen, K | Article | 21M21 |
