Researchers
Novaković, Ivana
Results 121-140 of 392
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2019 | Whole mitochondrial genome analysis in carriers of mt3460 mutation with Leber's hereditary optic neuropathy![]() | Dawod, Phepy G. A.; Rovčanin, Branislav R. | Conference Paper | Mp. category will be shown later |
| 2019 | Patofiziologija - mehanizmi poremećaja zdravlja - Deo 1.![]() | Čemerikić, Dušan; De Luka, Silvio | Text book | Mp. category will be shown later |
| 2019 | The frequency of C9orf72 repeat expansion beyond ALS/FTD spectrum in Serbian patients with neurodegenerative disorders![]() | Marjanović, Ana | Conference Paper | Mp. category will be shown later |
| 2019 | Genetic variant rs16944 in IL1B gene is a risk factor for early onset sepsis susceptibility and outcome in preterm infants![]() | Maksimović, Nela S. | Conference Paper | Mp. category will be shown later |
| 2019 | Association between Tumor Necrosis Factor-alpha Promoter-308 G/A Polymorphism and Early Onset Sepsis in Preterm Infants![]() | Varljen, Tatjana; Rakić, Olgica; Sekulović, Gordana; Jekić, Biljana | Article | 22M22 |
| 2019 | GLUT1 deficiency syndrome : a case report with a novel SLC2A1mutation![]() | Ivančević, Nikola | Article | 23M23 |
| 2019 | Angiogenin gene mutations in patients with amyotrophic lateral sclerosis from tertiary center in Belgrade![]() | Janković, Milena | Conference Paper | Mp. category will be shown later |
| 2019 | Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy![]() | Dawod, Phepy G. A.; Rovčanin, Branislav R.; Branković, Marija | Conference Paper | Mp. category will be shown later |
| 2019 | Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients![]() | Mitropoulos, Konstantinos; ...; Dobričić, Valerija S. | Conference Paper | Mp. category will be shown later |
| 2019 | Correlation of selected polymorphisms in COMT, DAT (SL6A3), DRD2, and ANKK1 genes and complications of long-term levodopa treatment in patients with idiopathic Parkinsons disease![]() | Radojević, Branislava | Conference Paper | Mp. category will be shown later |
| 2019 | Association of genetic markers of coagulation and fibrinolysis with prematurity complication![]() | Damnjanović, Tatjana M. | Conference Paper | Mp. category will be shown later |
| 2019 | Genetski zasnovana terapija neurodegenerativnih bolesti![]() | Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2019 | Polymorphisms in PPARG gene: Association with obesity-related metabolic traits in Serbian adolescent population![]() | Pešić, Milica M. | Conference Paper | Mp. category will be shown later |
| 2019 | The pattern of inheritance and genetic status in early onset Alzheimer's disease and frontotemporal dementia![]() | Mandić-Stojmenović, Gorana B. | Conference Paper | Mp. category will be shown later |
| 2019 | Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes![]() | Vidmar, Lovro; Maver, Ales; Drulović, Jelena | Article | 21M21 |
| 2019 | Significance of KIT and PDGFRA mutations in gastric gastrointestinal stromal tumor imatinib-naive surgically treated patients![]() | Ebrahimi, Keramatollah | Article | 23M23 |
| 2019 | Spectrum of mutations in presenilin 1 gene in patients with early onset Alzheimer disease![]() | Andabaka, Marko | Conference Paper | Mp. category will be shown later |
| 2019 | Genetika amiotrofične lateralne skleroze![]() | Stević, Zorica | Conference Paper | Mp. category will be shown later |
| 2019 | Clinical course of patients with pantothenate kinase-associated neurodegeneration (PKAN) before and after DBS surgery![]() | Svetel, Marina | Article | 21M21 |
| 2019 | Molecular genetic testing of Huntington’s disease and genetic counselling![]() | Mandić, Ratka; Marjanović, Ana | Conference Paper | Mp. category will be shown later |
