Researchers
Klaassen Ljubičić, Kristel
Results 1-20 of 80
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2026 | First Reported Use of Recombinant Parathyroid Hormone in Kenny–Caffey Syndrome Type 2: A Case Report and Literature Review | Milošević Đorđević, Maja; Skakić, Anita   ; Anđelković, Marina ; Delgado-Vega, Angelica Maria; Thonberg, Håkan; Klaassen, Kristel ; Komazec, Jovana; Kecman, Bozica; Jocić, Nikola ; Björck, Erik;
Lindstrand, Anna; Stojiljković, Maja
; | Article | 22M22 |
| 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 ; Anđelković, Marina ; Klaassen, Kristel ; Skakić, Anita ; Ugrin, Milena ; Pavlović, Sonja ; Nordgren, A.; Lindstrand, A.; Kjellqvist, S.; Matić, Lj.;
Stojiljković, Maja
; | Conference Paper | Mp. category will be shown later |
| 2025 | MITOCHONDRIAL MYOPATHY CAUSED BY MT-ND5 VARIANT: INTEGRATING WES AND MITOCHONDRIAL DNA ANALYSIS | Klaassen, Kristel ; Djordjević, Maja; Kecman, Božica; Pavlović, Djordje; Stanković, Sara ; Andjelković, Marina ; Skakić, Anita ; Ugrin, Milena ; Komazec, Jovana ; Stojiljkovi, Maja | 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 ; Parezanović, Marina ; Stevanović, Nina ; Andjelković, Marina ; Ugrin, Milena ; Spasovski, Vesna ; Klaassen, Kristel ; Komazec, Jovana ; Stojiljković, Maja ; 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 ; Kecman, B; Stankovic, S ; Komazec, Jovana ; Pavlovic, S ; Stojiljkovic, Maja ; Djordjevic, M | Article | 21M21 |
| 2025 | Multiphasic acute disseminated encephalomyelitis (MDEM) in a patient with systemic lupus erythematosus and C4A deficiency: case-based review | Ljubičić, Jelena ; Klaassen, Kristel M. ; Karić, Uroš ; Stanković, Ana; Petrović, Gordana; Mišković, Rada ; Stjepanović, Mirjana M.; Pavlović, Sonja T. ; Stojanović, Maja R. | Article | 21M21 |
| 2024 | Transcriptome Profiling of Phenylalanine-Treated Human Neuronal Model: Spotlight on Neurite Impairment and Synaptic Connectivity | Stankovic, Sara ; Lazic, Andrijana ; Parezanovic, Marina ; Stevanovic, Milena J ; Pavlovic, Sonja ; Stojiljkovic, Maja ; Klaassen, Kristel M | Article | 21M21 |
| 2024 | CHARACTERIZATION OF 16 NOVEL GENETIC VARIANTS IN GENES ASSOCIATED WITH EPILEPSY | Anđelković, Marina ; Klaassen, Kristel ; Skakić, Anita ; Marjanović, Irena ; Kravljanac, Ružica; Đorđević, Maja; Vučetić Tadić, Biljana; Kecman, Božica; Pavlović, Sonja ; Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2024 | Case report: Rapidly progressive neurocognitive disorder with a fatal outcome in a patient with PU.1 mutated agammaglobulinemia | Mišković, Rada ; Ljubičić, Jelena ; Bonači-Nikolić, Branka ; Petković, Ana; Marković, Vladana ; Ranković, Ivan ; Đorđević, Jelena ; Stanković, Ana; Klaassen, Kristel ; Pavlović, Sonja ;
Stojanović, Maja
; | Article | 21M21 |
| 2024 | Genetic landscape of phenylketonuria in Serbia | Klaassen, Kristel ; Sara, Stanković ; Đorđević Milošević, Maja; Božica, Kecman; Anđelković, Marina ; Skakić, Anita ; Spasovski, Vesna ; Ugrin, Milena ; Komazec, Jovana ; Parezanović, Marina ;
Jocić, Nikola
; Stevanović, Nina ; Pavlović, Sonja ; Stojiljković, Maja ; | Conference Paper | Mp. category will be shown later |
| 2024 | INVESTIGATING THE GENETIC COMPLEXITY OF NEUTROPENIA IN PEDIATRIC PATIENTS WITH GLYCOGEN STORAGE DISEASE IB: A MODIFIER GENE PERSPECTIVE | Skakić, Anita ; Parezanović, Marina ; Pavlović, Đorđe ; Stevanović, Nina ; Anđelković, Marina ; Klaassen, Kristel ; Ugrin, Milena ; Komazec, Jovana ; Spasovski, Vesna ; Đorđević, Maja;
Stojiljković, Maja
; | Conference Paper | Mp. category will be shown later |
| 2024 | Molecular genetic basis of childhood epilepsy in Serbia: utility of clinical and whole exome sequencing | Anđelković, M. ; Klaassen, Kristel ; Skakić, Anita ; Marjanović, I. ; Kravljanac, R.; Đorđević, M.; Vučetić Tadić, B.; Kecman B.; Pavlović, Sonja ; Stojiljković, M. | Conference Paper | Mp. category will be shown later |
| 2024 | WGS approach to identify potential genetic modifiers in Glycogen Storage Disease Ib | Skakić, Anita ; Parezanović, Marina ; Pavlović, Đorđe ; Srevanović, N.; Anđelković, M. ; Klaassen, Kristel ; Ugrin, Marija ; Komazec, Jovana ; Spasovski, Vesna ; Đorđević, M.;
Pavlović, S.
; Stojiljković, M. ; | Conference Paper | Mp. category will be shown later |
| 2024 | Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies | Anđelković, Marina ; Klaassen, Kristel ; Skakić, Anita ; Marjanović, Irena ; Kravljanac, Ružica ; Đorđević, Maja ; Vučetić-Tadić, Biljana ; Kecman, Božica; Pavlović, Sonja ; Stojiljković, Maja | Article | 21M21 |
| 2024 | MOLECULAR BASIS OF PHENYLKETONURIA IN SERBIAN PAEDIATRIC COHORT | Klaassen, Kristel ; Đorđević Milošević, Maja; Kecman, Božica; Anđelković, Marina ; Skakić, Anita | Conference Paper | Mp. category will be shown later |
| 2024 | Transcriptome profile of phenylalanine treated NT2-derived neurons – a step towards novel PKU model system PO-576 | Stanković, Sara ; Lazić, Andrijana ; Stevanović, Milena ; Anđelković, Marina ; Parezanović, Marina ; Pavlović, Sonja ; Stojiljković, Maja ; Klaassen, Kristel | Conference Paper | Mp. category will be shown later |
| 2024 | Characterization of 16 novel genetic variants in genes associated with paediatric epilepsy: implications for targeted therapeutic strategies | Anđelković, Marina ; Klaassen, Kristel ; Skakić, Anita ; Marjanović, Irena ; Kravljanac, Ružica ; Đorđević, Maja ; Vučetić Tadić, Biljana ; Kecman, Božica; Pavlović, Sonja ; Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2023 | Improving the diagnostics of rare lung disorders using a uniquely designed pipeline for analysis of ngs data | Anđelković, Marina ; Skakić, Anita ; Stevanović, Nina ; Parezanović, Marina ; Komazec, Jovana ; Klaassen, Kristel ; Spasovski, Vesna ; Stojiljković, Maja ; Pavlović, Sonja | Conference Paper | Mp. category will be shown later |
| 2023 | THE IMPACT OF NEXT-GENERATION SEQUENCING ON DIAGNOSIS AND TREATMENT OF RARE DISEASES | Stojiljković, Maja ; Ugrin, Milena ; Klaassen, Kristel ; Skakić, Anita ; Anđelković, Marina ; Komazec, Jovana ; Spasovski, Vesna ; Pavlović, Sonja | Conference Paper | Mp. category will be shown later |
| 2023 | Application of CRISPR/cas9 technology for in vitro disease modelling in glycogen storage disease type IB | Parezanović, Marina ; Anđelković, Marina ; Stevanović, Nina ; Klaassen, Kristel ; Spasovski, Vesna ; Ugrin, Milena ; Komazec, Jovana ; Stanković, Sara ; Jocić, Nikola ; Pavlović, Sonja ;
Stojiljković, Maja
; Skakić, Anita ; | Conference Paper | Mp. category will be shown later |