Researchers
Stojiljković, Maja
Type
Date issued
Results 81-100 of 137
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2017 | Functional and structural characterisation of 5 missense mutations of the phenylalanine hydroxylase | Pecimonova, Martina; Polak, Emil; Csicsay, Frantisek; Reblova, Kamila; Stojiljković, Maja | Article | 23M23 |
| 2017 | Correction: A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics | Mizzi, Clint; Dalabira, Eleni; Kumuthini, Judit; Dzimiri, Nduna; Balogh, Istvan; Başak, Nazli; Böhm, Ruwen; Borg, Joseph; Borgiani, Paola; Bozina, Nada;
Bruckmueller, Henrike; Burzynska, Beata; Carracedo, Angel; Cascorbi, Ingolf; Deltas, Constantinos; Dolzan, Vita; Fenech, Anthony; Grech, Godfrey; Kasiulevicius, Vytautas; Kádaši, Ľudevít; Kučinskas, Vaidutis; Khusnutdinova, Elza; Loukas, Yiannis L.; Macek, Milan; Makukh, Halyna; Mathijssen, Ron; Mitropoulos, Konstantinos; Mitropoulou, Christina; Novelli, Giuseppe; Papantoni, Ioanna; Pavlović, Sonja
| Other | Mp. category will be shown later |
| 2017 | Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies | Viennas, Emmanouil; Komianou, Angeliki; Mizzi, Clint; Stojiljković, Maja | Article | 21a+M21a+ |
| 2017 | Genetic modifiers of beta-thalassemia: a rise of a novel therapy approaches.![]() | Milena Ugrin; Stojiljkovic, Maja | Conference Paper | Mp. category will be shown later |
| 2016 | Kliničke karakteristike i genotip bolesnika sa glikogenozom tip 1![]() | Adrijan Sarajlija; Đorđevic, Maja; Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 2016 | Gene Mutation Profiles in Primary Diffuse Large B Cell Lymphoma of Central Nervous System: Next Generation Sequencing Analyses![]() | Todorović-Balint, Milena | Article | 21M21 |
| 2016 | Molecular and phenotypic characteristics of seven novel mutations causing branched-chain organic acidurias![]() | Stojiljković, Maja | Article | 21M21 |
| 2016 | Nutrigenomics and nutriepigenomics: on the road to personalized nutrition![]() | Pavlović, Sonja | Conference Paper | Mp. category will be shown later |
| 2016 | Functional Analysis of an (A)gamma-Globin Gene Promoter Variant (HBG1: g.-225_-222delAGCA) Underlines Its Role in Increasing Fetal Hemoglobin Levels Under Erythropoietic Stress![]() | Ugrin, Milena | Article | 23M23 |
| 2016 | A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics | Mizzi, Clint; Dalabira, Eleni; Kumuthini, Judit; Dzimiri, Nduna; Balogh, Istvan; Basak, Nazli; Boehm, Ruwen; Borg, Joseph; Borgiani, Paola; Bozina, Nada;
Bruckmueller, Henrike; Burzynska, Beata; Carracedo, Angel; Cascorbi, Ingolf; Deltas, Constantinos; Dolzan, Vita; Fenech, Anthony; Grech, Godfrey; Kasiulevicius, Vytautas; Kadasi, L'udevit; Kucinskas, Vaidutis; Khusnutdinova, Elza; Loukas, Yiannis L.; Macek, Milan, Jr.; Makukh, Halyna; Mathijssen, Ron; Mitropoulos, Konstantinos; Mitropoulou, Christina; Novelli, Giuseppe; Papantoni, Ioanna; Pavlović, Sonja
| Article | 21M21 |
| 2016 | Molecular genetic testing of inborn metabolic diseases in Serbia![]() | Stojiljkovic, Maja | Conference Paper | Mp. category will be shown later |
| 2015 | Molecular characterization of mutations in Serbian patients with glycogen storage diseases.![]() | Skakic, Anita | Conference Paper | Mp. category will be shown later |
| 2015 | Molecular genetic study of congenital adrenal hyperplasia in serbia: two novel CYP21A2 gene mutations![]() | Skakic, Anita | Conference Paper | Mp. category will be shown later |
| 2015 | Novel Therapy Approaches in β-Thalassemia Syndromes — A Role of Genetic Modifiers | Pavlović, Sonja | Book parts | Mp. category will be shown later |
| 2015 | Genetička osnova urođenih bolesti metabolizma u Srbiji![]() | Stojiljkovic, Maja | Conference Paper | Mp. category will be shown later |
| 2015 | Successful dietary management of severe hyperlipidemia in patients with glycogen storage disease type 1![]() | Bozica Kecman; Đordjević, Maja; Skakić, Anita | Conference Paper | Mp. category will be shown later |
| 2015 | Molecular genetic study of congenital adrenal hyperplasia in Serbia: novel p.Leu129Pro and p.Ser165Pro CYP21A2 gene mutations![]() | Milačić, I.; Barać, M.; Milenković, Tatjana; Ugrin, Milena | Article | 22M22 |
| 2015 | Molecular characterization of mutations in Serbian patients with glycogen storage diseases - an NGS approach![]() | Skakic, Anita | Conference Paper | Mp. category will be shown later |
| 2015 | Phenylketonuria screening and management in southeastern Europe - survey results from 11 countries | Zerjav, Tansek Mojca; Groselj, Urh; Angelkova, Natalija; Anton, Dana; Baric, Ivo; Djordjevic, Maja; Grimci, Lindita; Ivanova, Maria; Kadam, Adil; Kotori, Vjosa;
Maksic, Hajrija; Marginean, Oana; Margineanu, Otilia; Miljanovic, Olivera; Moldovanu, Florentina; Muresan, Mariana; Nanu, Michaela; Samardzic, Mira; Sarnavka, Vladimir; Savov, Aleksei; Stojiljković, Maja
| Article | 21aM21a |
| 2015 | Novel p.Gln226Lys mutation in phenylalanine hydroxylase gene resulting in classical PKU![]() | Klaassen Kristel | Conference Paper | Mp. category will be shown later |
