Autori: Stojiljkovic Maja M
Naslov | Clinical and Genetic Profile of 35 Patients with Glycogen Storage Disease Type 1b: A Comparative Analysis Before and During SGLT2 Inhibitor Therapy (Article; Early Access) |
Autori | Djordjevic-Milosevic Maja Skakic Anita G ![]() |
Info | MOLECULAR DIAGNOSIS & THERAPY, (2025), vol. br. , str. - |
Projekat | Science Fund of the Republic of Serbia, Prisma program [6999]; Ministry of Science, Technological Development and Innovation of the Republic of Serbia [451-03-136/2025-03/200042] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
|
Naslov | Genomic profiling, implications for genotype-based treatment of 131 patients with phenylketonuria and characterization of novel p.Pro416Leu PAH variant (Article) |
Autori | Klaassen Kristel M Kecman Bozica Stankovic S Komazec Jovana Pavlovic Sonja T Stojiljkovic Maja M Djordjevic M |
Info | SCIENTIFIC REPORTS, (2025), vol. 15 br. 1, str. - |
Projekat | Horizon Europe Project BRIDGING-RD [HORIZON-WIDERA-2023-ACCESS-02, 101160079]; Ministry of Science, Technological Development and Innovation of the Republic of Serbia [451-03-136/2025-03/200042] |
Ispravka | Web of Science Članak Elečas Rang časopisa |
|
Naslov | Phenylbutyric Acid Modulates Apoptosis and ER Stress-Related Gene Expression in Glycogen Storage Disease Type Ib In Vitro Model (Article) |
Autori | Parezanovic Marina V Stevanovic Nina ![]() ![]() |
Info | MOLECULAR GENETICS & GENOMIC MEDICINE, (2025), vol. 13 br. 1, str. - |
Projekat | Science Fund of the Republic of Serbia [6999] |
Ispravka | Web of Science Članak Elečas Rang časopisa |
|
Naslov | The Importance of Early Detecting of Thyroid Dysfunction During Pregnancy and Association with Gestational Diabetes Mellitus (Article) |
Autori | Todorovic Jovana S ![]() ![]() ![]() ![]() ![]() ![]() |
Info | ACTA ENDOCRINOLOGICA-BUCHAREST, (2024), vol. 20 br. 2, str. 153-161 |
Ispravka | Web of Science Članak Elečas Rang časopisa |
|
Naslov | Transcriptome Profiling of Phenylalanine-Treated Human Neuronal Model: Spotlight on Neurite Impairment and Synaptic Connectivity (Article) |
Autori | Stankovic Sara S Lazic Andrijana ![]() ![]() |
Info | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, (2024), vol. 25 br. 18, str. - |
Projekat | Ministry of Science, Technological Development and Innovation of the Republic of Serbia; [451-03-66/2024-03/200042] |
Ispravka | Web of Science Članak Elečas Rang časopisa |
|
Naslov | Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies (Article; Early Access) |
Autori | Andjelkovic Marina Z Klaassen Kristel M Skakic Anita G ![]() ![]() |
Info | MOLECULAR DIAGNOSIS & THERAPY, (2024), vol. br. , str. - |
Projekat | Ministry of Science, Technological Development and Innovations Republic of Serbia [451-03-66/2024-03/200042] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
|
Naslov | Seven-Year Longitudinal Study: Clinical Evaluation of Knee Osteoarthritic Patients Treated with Mesenchymal Stem Cells (Article) |
Autori | Spasovski Dusko V ![]() ![]() |
Info | JOURNAL OF CLINICAL MEDICINE, (2024), vol. 13 br. 13, str. - |
Projekat | Ministry of Science, Technological Development and Innovation, Republic of Serbia [451-03-66/2024-03/200042, 2024] |
Ispravka | Web of Science Članak Elečas Rang časopisa |
|
Naslov | Comparison of the ABC and ACMG systems for variant classification (Article; Early Access) |
Autori | Houge Gunnar ... Keckarevic-Markovic Milica ... Jankovic Milena Z ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. br. , str. - |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
|
Naslov | Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier (Meeting Abstract) |
Autori | Klaassen Kristel M Djordjevic Maja S Skakic Anita G ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 433-433 |
Projekat | MESTD-RS [451-03-68/2022-14/200042] |
Ispravka | Web of Science Elečas Rang časopisa |
|
Naslov | Molecular diagnosis of Fabry disease in patients with chronic renal failure of unknown etiology (Meeting Abstract) |
Autori | Parezanovic Marina V Stojiljkovic Maja M Andjelkovic Marina Z Stevanovic Nina ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 432-433 |
Projekat | Takeda GmbH, Serbia |
Ispravka | Web of Science Elečas Rang časopisa |
|