Researchers
Stojiljković, Maja
Results 101-120 of 137
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2015 | Next generation sequencing role in diagnosis of mitochondrial disease in Serbian patient![]() | Đorđević, Maja; Stojiljković, 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: two novel CYP21A2 gene mutations![]() | Skakic, Anita | Conference Paper | Mp. category will be shown later |
| 2015 | Novel Patched 1 mutations in patients with nevoid basal cell carcinoma syndrome - case report![]() | Škodrić Trifunović, Vesna | Article | 22M22 |
| 2014 | Newborn screening in southeastern Europe | Groselj, Urh; Tansek, Mojca Zerjav; Smon, Andraz; Angelkova, Natalija; Anton, Dana; Baric, Ivo; Djordjevic, Maja; Grimci, Lindita; Ivanova, Maria; Kadam, Adil;
Kotori, Vjosa Mulliqi; Maksic, Hajrija; Marginean, Oana; Margineanu, Otilia; Milijanovic, Olivera; Moldovanu, Florentina; Muresan, Mariana; Murko, Simona; Nanu, Michaela; Lampret, Barbka Repic; Samardzic, Mira; Sarnavka, Vladimir; Savov, Aleksei; Stojiljković, Maja
| Article | 22M22 |
| 2014 | Molekularno-genetički markeri kao osnov za personalizovanu medicinu | Pavlović, Sonja | Article | 23M23 |
| 2014 | Molecular genetic characteristics of hyperphenylalaninemias in Serbia and implications for personalized medicine.![]() | Stojiljković Maja | Conference Paper | Mp. category will be shown later |
| 2014 | Association of gene variants in TLR4 and IL-6 genes with perthes disease![]() | Srzentić, Sanja | Article | 23M23 |
| 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 | Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin![]() | Radmilović Milena | Article | 22M22 |
| 2013 | The influence of novel transcriptional regulatory element in intron 14 on the expression of Janus kinase 2 gene in myeloproliferative neoplasms![]() | Spasovski, Vesna | Article | 22M22 |
| 2013 | Association of mitochondrial DNA variants and cognitive impairment of phenylketonuria patients![]() | Klaassen Kristel | Article | 23M23 |
| 2013 | Genomic variation in the MAP3K5 gene is associated with beta-thalassemia disease severity and hydroxyurea treatment efficacy![]() | Tafrali, Christina; Paizi, Arsinoi; Borg, Joseph; Radmilović Milena | Article | 21M21 |
| 2012 | Genotype-phenotype analysis of Serbian p.l48s pku patients | Stojiljković, Maja | Conference Paper | Mp. category will be shown later |
| 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 |
| 2012 | 6th Golden Helix Pharmacogenomics Day: pharmacogenomics and individualized therapy | Stojiljković, Maja | Contribution to periodical | Mp. category will be shown later |
| 2012 | The 46/1 haplotype is involved in transcriptional regulation of janus kinase 2 gene | Spasovski, Vesna | Conference Paper | Mp. category will be shown later |
| 2012 | A novel KLF1 gene promoter variant (g.-148 g gt a) is associated with hereditary persistence of fetal hemoglobin | Radmilović, M. | Conference Paper | Mp. category will be shown later |
