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European Journal of Medical Genetics|September 20, 2019
Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type IbAdrijan Sarajlija, Maja Djordjevic, Bozica Kecman, et al.
European Journal of Haematology|October 2, 2004
Acquired amegakaryocytic thrombocytopenia associated with proliferation of gamma/delta TCR T-lymphocytes and a BCR-ABL (p210) fusion transcriptMilica Colovic, Sonja Pavlovic, Nada Kraguljac, et al.
Endocrine|March 14, 2021
A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasiaVioleta Anastasovska, Mirjana Kocova, Nikolina Zdraveska, et al.
Molecular Genetics & Genomic Medicine|January 13, 2025
Phenylbutyric Acid Modulates Apoptosis and ER Stress-Related Gene Expression in Glycogen Storage Disease Type Ib In Vitro ModelMarina Parezanovic, Nina Stevanovic, Marina Andjelkovic, et al.
Molecular Biology Reports|August 30, 2020
Analysis of the promoter regions of disease-causing genes in maturity-onset diabetes of the young patientsJovana Komazec, Bojan Ristivojevic, Branka Zukic, et al.
Molecular Diagnosis & Therapy|June 19, 2025
Clinical and Genetic Profile of 35 Patients with Glycogen Storage Disease Type 1b: A Comparative Analysis Before and During SGLT2 Inhibitor TherapyMaja Djordjevic Milosevic, Anita Skakic, Bozica Kecman, et al.
Clinical Biochemistry|June 26, 2012
Overexpression of the novel member of the BCL2 gene family, BCL2L12, is associated with the disease outcome in patients with acute myeloid leukemiaHellinida Thomadaki, Konstantinos V Floros, Sonja Pavlovic, et al.
Diagnostics (Basel, Switzerland)|January 21, 2022
Expression Profiles of Long Non-Coding RNA GAS5 and MicroRNA-222 in Younger AML PatientsDjordje Pavlovic, Natasa Tosic, Branka Zukic, et al.
Molecular Genetics and Metabolism|July 6, 2010
Novel transcriptional regulatory element in the phenylalanine hydroxylase gene intron 8Maja Stojiljkovic, Branka Zukic, Natasa Tosic, et al.
Frontiers in Immunology|April 17, 2026
Behçet's syndrome-like features revealing myelodysplastic syndrome with TP53 mutation: a case reportAndrej Pesic, Jelena Ljubicic, Milena Todorovic Balint, et al.
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