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Autori: Stojiljkovic Maja M

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Vidi i: Stojiljkovic-Petrovic 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  Kecman Bozica Stankovic Sara S Kovacevic Ivona Pavlovic Sonja T Stojiljkovic Maja M 
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]
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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]
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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  Andjelkovic Marina Z Ugrin Milena M Pavlovic Sonja T Stojiljkovic Maja M Skakic Anita G  
Info MOLECULAR GENETICS & GENOMIC MEDICINE, (2025), vol. 13 br. 1, str. -
Projekat Science Fund of the Republic of Serbia [6999]
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Naslov The Importance of Early Detecting of Thyroid Dysfunction During Pregnancy and Association with Gestational Diabetes Mellitus (Article)
Autori Todorovic Jovana S  Dugalic Stefan V  Jovandaric Miljana Z  Stojiljkovic Maja M Pantic Igor V  Macura Maja M  Perkovic Sonja Milincic Milos  Sengul D Sengul I Gojnic Miroslava G 
Info ACTA ENDOCRINOLOGICA-BUCHAREST, (2024), vol. 20 br. 2, str. 153-161
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Naslov Transcriptome Profiling of Phenylalanine-Treated Human Neuronal Model: Spotlight on Neurite Impairment and Synaptic Connectivity (Article)
Autori Stankovic Sara S Lazic Andrijana  Parezanovic Marina V Stevanovic Milena J  Pavlovic Sonja T Stojiljkovic Maja M Klaassen Kristel M 
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]
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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  Marjanovic Irena M  Kravljanac Ruzica M Djordjevic Maja S Vucetic-Tadic Biljana Kecman Bozica Pavlovic Sonja T Stojiljkovic Maja M 
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]
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Naslov Seven-Year Longitudinal Study: Clinical Evaluation of Knee Osteoarthritic Patients Treated with Mesenchymal Stem Cells (Article)
Autori Spasovski Dusko V  Spasovski Vesna M  Bascarevic Zoran Lj Stojiljkovic Maja M Andjelkovic Marina Z Pavlovic Sonja T 
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]
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Naslov Comparison of the ABC and ACMG systems for variant classification (Article; Early Access)
Autori Houge Gunnar ... Keckarevic-Markovic Milica ... Jankovic Milena Z  ... Stojiljkovic Maja M ... (broj koautora 48) 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. br. , str. -
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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  Kecman Bozica Parezanovic Marina V Andjelkovic Marina Z Stevanovic Nina  Spasovski Vesna M  Ugrin Milena M Drmanac Radoje Pavlovic Sonja T Stojiljkovic Maja M 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 433-433
Projekat MESTD-RS [451-03-68/2022-14/200042]
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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  Spasovski Vesna M  Ugrin Milena M Komazec Jovana Tosic Natasa M  Pavlovic Sonja T Celic Dejan  Vucenovic Jelica Skakic Anita G  
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 432-433
Projekat Takeda GmbH, Serbia
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Vidi i: Stojiljkovic-Petrovic Maja M

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