Researchers
Novaković, Ivana
Results 221-240 of 394
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2015 | Pharmacogenetics of drug response in Parkinson's disease![]() | Džoljić, Eleonora | Article | 23M23 |
| 2015 | Effect of accumulation of 5-HTTLPR, BDNF Vall66Met and COMT Val158Met polymorphisms on brain morphology in patients with major depressive disorder![]() | Kostic, Milutin V; Canu, Elisa; Munjiza, Ana M; Agosta, Federica; Novakovic, Ivana V
Filippi, Massimo;
| Conference Paper | Mp. category will be shown later |
| 2015 | Further evidence of the impact of the risk variant FKBP5 gene in schizophrenia in a Serbian sample of patients, siblings and controls![]() | Mihaljević, Marina | Conference Paper | Mp. category will be shown later |
| 2015 | Echocardiography in patients with myotonic dystrophy type 1![]() | Perić, Stojan Z. | Conference Paper | Mp. category will be shown later |
| 2015 | Three-way interaction of 5-HTTLPR, BDNF Vall66Met and COMT Val158Met polymorphisms and its effect on regional gray matter volume in patients with major depressive disorder![]() | Canu, Elisa; Kostic, Milutin V; Munjiza, Ana M; Agosta, Federica; Novakovic, Ivana V | Conference Paper | Mp. category will be shown later |
| 2015 | Presenting symptoms of GBA-related Parkinson's disease![]() | Kresojević, Nikola | Article | 21M21 |
| 2015 | Mreža za neuromišićne bolesti Srbije (NMD-SerbNet)![]() | Brkušanin, Miloš | Conference Paper | Mp. category will be shown later |
| 2015 | Variability of multisystemic features in myotonic dystrophy type 1 – lessons from Serbian registry![]() | Rakočević-Stojanović, Vidosava | Article | 22M22 |
| 2015 | GSTO1*C/GSTO2*G haplotype is associated with risk of transitional cell carcinoma of urinary bladder![]() | Đukić, Tatjana | Article | 22M22 |
| 2015 | Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population![]() | Janković, Milena Z. | Article | 22M22 |
| 2015 | Presenting symptoms of GBA-related Parkinson's disease![]() | Kresojević, Nikola D. | Conference Paper | Mp. category will be shown later |
| 2015 | Subtelomeric screening in Serbian children with dysmorphic features and unexplained developmental delay/intellectual disabilities![]() | Damnjanović, Tatjana | Article | 23M23 |
| 2015 | Varijabilnost multisistemske afekcije u miotoničnoj distrofiji tip 1 - pouke iz srpskog registra![]() | Rakočević-Stojanović, Vidosava | Conference Paper | Mp. category will be shown later |
| 2015 | Intellectual ability in the Duchenne muscular dystrophy and dystrophin gene mutation location![]() | Milić-Rašić, Vedrana | Article | 23M23 |
| 2015 | Metabolic syndrome in patients with myotonic dystrophy type 1![]() | Vujnić, Milorad; Perić, Stojan | Article | 22M22 |
| 2015 | Screening for C9orf72 Expansion Mutation in Serbian Patients with Early-Onset Dementia![]() | Mandić-Stojmenović, Gorana | Article | 21M21 |
| 2015 | The association of ZNF366 gene and PTPRD gene polymorphisms with plasma homocysteine level in patients on hemodialysis | Maksimović, Nela S. | Conference Paper | Mp. category will be shown later |
| 2014 | NMD SerbNet - integrativni pristup u dijagnostici neuromišićnih bolesti u Srbiji![]() | Milić-Rašić, Vedrana | Article | 52M52 |
| 2014 | Neurogenetika u eri 'omika' | Novaković, Ivana | Book parts | Mp. category will be shown later |
| 2014 | Executive function and visual memory computerized testing in myotonic dystrophies![]() | Perić, Stojan | Conference Paper | Mp. category will be shown later |
