Milena Ugrin

Molecular genetic study of congenital adrenal hyperplasia in Serbia: novel p.Leu129Pro and p.Ser165Pro CYP21A2 gene mutations

Iva Milacic, Miroljub Barać, Tatjana Milenković et al. · Journal of Endocrinological Investigation · 2015 · 34 citations

Adrenal Gland, Molecular Genetic Study, Congenital Adrenal Hyperplasia +10

Use of Wilms Tumor 1 Gene Expression as a Reliable Marker for Prognosis and Minimal Residual Disease Monitoring in Acute Myeloid Leukemia With Normal Karyotype Patients

Irena Marjanović, Teodora Karan-Djurašević, Milena Ugrin et al. · Clinical Lymphoma Myeloma & Leukemia · 2017 · 32 citations

Hematological Malignancy, Tumor Biology, Oncology +14

Molecular Genetics and Genotype-Based Estimation of BH4-Responsiveness in Serbian PKU Patients: Spotlight on Phenotypic Implications of p.L48S

Maja Djordjevic, Kristel Klaassen, Adrijan Sarajlija et al. · JIMD Reports · 2012 · 27 citations · Full text

Genetic characterization of <scp>GSD</scp> I in Serbian population revealed unexpectedly high incidence of <scp>GSD</scp> Ib and 3 novel <i><scp>SLC37A4</scp></i> variants

Anita Skakić, Maja Djordjevic, Adrijan Sarajlija et al. · Clinical Genetics · 2017 · 25 citations

Expression of TLR7, TLR9, JAK2, and STAT3 genes in peripheral blood mononuclear cells from patients with systemic sclerosis

Miša Vreća, Ana Zeković, Nemanja Damjanov et al. · Journal of Applied Genetics · 2017 · 16 citations

Inflammation, Cytokine, Autoimmune Disease +9