Researchers
Klaassen Ljubičić, Kristel
Results 61-80 of 80
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2017 | Precision molecular diagnostic of hepatic GSD revealed unexpectedly high incidence of gsd ib in serbian population and three novel variants in the SLC37A4 gene![]() | Skakic, Anita | Conference Paper | Mp. category will be shown later |
| 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 | Molecular and phenotypic characteristics of seven novel mutations causing branched-chain organic acidurias![]() | Stojiljković, Maja | Article | 21M21 |
| 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 | Functional analysis of an Aγ-globin gene promoter variant (HBG1: g.-225_-222delAGCA) underlines its role in increasing fetal hemoglobin levels under erythropoietic stress![]() | Jovana Komazec | Conference Paper | Mp. category will be shown later |
| 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 | 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 | Tetrahydrobiopterin deficiency among Serbian patients presenting with hyperphenylalaninemia![]() | Stojiljković, Maja | Article | 23M23 |
| 2015 | Functional analysis of the four base pair deletion upstream of the Aγ-globin gene associated with decreased gene expression![]() | Jovana Komazec | Conference Paper | Mp. category will be shown later |
| 2015 | Influence of Promoter Polymorphisms of the Tnf-α (-308g/A) and IL-6 (-174g/C) Genes on Therapeutic Response to Etanercept in Rheumatoid Arthritis | Jančić, Ivan | Article | 23M23 |
| 2015 | Molecular genetic testing of inborn metabolic diseases in Serbia![]() | Stojiljkovic, Maja | Conference Paper | Mp. category will be shown later |
| 2014 | Molecular genetic characteristics of hyperphenylalaninemias in Serbia and implications for personalized medicine.![]() | Stojiljković Maja | Conference Paper | Mp. category will be shown later |
| 2014 | Molekularne karakteristike, fenotipska raznolikost i procena odgovora na terapiju zasnovana na genotipu kod srpskih pacijenata sa fenilketonurijom![]() | Stojiljković, Maja | Article | 23M23 |
| 2014 | Association of variants in FTO, FABP2, PPARG, ADRB2 and ADRB3 genes with obesity in Serbian population: A prerequisite for nutrigenetic algorithm development.![]() | Skakić, Anita | Conference Paper | Mp. category will be shown later |
| 2013 | Association of mitochondrial DNA variants and cognitive impairment of phenylketonuria patients![]() | Klaassen Kristel | Article | 23M23 |
| 2012 | Molecular genetics and genotype-based estimation of BH4-responsiveness in serbian PKU patients: Spotlight on phenotypic implications of p.L48S![]() | Đorđević, M. | Article | Mp. category will be shown later |
| 2012 | 6-mercaptopurine influences TPMT gene transcription in a TPMT gene promoter variable number of tandem repeats-dependent manner![]() | Kotur, Nikola | Article | 21M21 |
