Researchers
Novaković, Ivana
Results 181-200 of 392
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2017 | Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis![]() | Maver, Ales; Lavtar, Polona; Ristić, Smiljana; Stopinšek, Sanja; Simčič, Saša; Hočevar, Keli; Sepčić, Juraj; Drulović, Jelena
Hodžić, Alenka; Rudolf, Gorazd; Šega, Saša; Starčević-Čizmarević, Nada; Palandačić, Anja; Zamolo, Gordana; Kapović, Miljenko; Likar, Tina; Peterlin, Borut;
| Article | 21aM21a |
| 2017 | Genetic variation in leptin and leptin receptor genes as a risk factor for idiopathic male infertility![]() | Hodžić, Alenka; Ristanović, Momčilo | Article | 21M21 |
| 2017 | PANK2 gene mutation spectrum in Serbian patients with neurodegeneration with brain iron accumulation![]() | Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2017 | First report of angiogenin gene mutations in patients with amyotrophic lateral sclerosis in Serbia![]() | Janković, Milena | Conference Paper | Mp. category will be shown later |
| 2017 | The presence of premutation in the FMR1 gene in patients with clinical picture of degenerative ataxia, tremor and parkinsonism![]() | Pešić, Milica | Conference Paper | Mp. category will be shown later |
| 2017 | Transcranial sonography in dopa-responsive dystonia![]() | Svetel, Marina | Article | 21M21 |
| 2017 | The Signature of Trauma in Psychosis: A Preliminary Genetic and Epigenetic Analyses of FK506-Binding Protein 5 Regulation![]() | Marić-Bojović, Nađa | Conference Paper | Mp. category will be shown later |
| 2017 | GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia![]() | Dobričić, Valerija | Article | 21aM21a |
| 2017 | Genotype-phenotype correlation in Friedreich's ataxia![]() | Kovačević, G.; Todorović, S.; Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2016 | Five-year study of quality of life in myotonic dystrophy![]() | Perić, Stojan | Article | 21M21 |
| 2016 | Genetic mutations in Frontemporal dementia - report from the memory clinic from Serbia![]() | Stefanova, Elka D. | Conference Paper | Mp. category will be shown later |
| 2016 | The cumulative effect of genetic polymorphisms on depression and brain structural integrity![]() | Kostić, Milutin
Filippi, Massimo;
| Article | 21a+M21a+ |
| 2016 | Cytomegalovirus induces Interleukin-6 mediated inflammatory response in salivary gland cancer![]() | Radunović, Milena | Article | 23M23 |
| 2016 | Clients' Perception of Outcome of Team-Based Prenatal and Reproductive Genetic Counseling in Serbian Service Using the Perceived Personal Control (PPC) Questionnaire![]() | Čuturilo, Goran | Article | 22M22 |
| 2016 | Udruženost uticaja haplotipa FKBP5 gena i traume u detinjstvu na rizik od psihotičnog poremećaja![]() | Mihaljević, Marina | Conference Paper | Mp. category will be shown later |
| 2016 | Association of 63/91 length polymorphism in the DHFR gene major promoter with toxicity of methotrexate in patients with rheumatoid arthritis![]() | Jekić, Biljana | Article | 21M21 |
| 2016 | Predictive role of circulating leucocyte-platelet aggregates for thromboembolic complications in philadelphia-negative myeloproliferative neoplasms: a prospective study![]() | Sefer, Dijana; Miljić, Predrag | Conference Paper | Mp. category will be shown later |
| 2016 | The MMP-2 and MMP-9 promoter polymorphisms and susceptibility to salivary gland cancer![]() | Radunović, Milena | Article | 23M23 |
| 2016 | Analysis of T-786C and 4a/b endothelial nitric oxide synthase gene polymorphisms in retinopathy of prematurity![]() | Pantelić, Jelica; Varljen, Tatjana; Maksimović, Nela | Article | 23M23 |
| 2016 | Humana genetika: sveska za praktične radove![]() | Luković, Ljiljana | Text book | Mp. category will be shown later |
