Researchers
Novaković, Ivana
Results 261-280 of 392
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2013 | Analiza rearanžmana u genu za distrofin primenom metode multipleks amplifikacije ligiranih proba | Pešović, Jovan | Conference Paper | Mp. category will be shown later |
| 2013 | Association of the TYMS 3G/3G genotype with poor response and GGH 354GG genotype with the bone marrow toxicity of the methotrexate in RA patients | Jekić, Biljana | Article | 21M21 |
| 2013 | Kliničke i imidžing karakteristike Parkinsonove bolesti vezane za mutaciju u genu za glukocerebrozidazu | Mijajlović, Milija | Conference Paper | Mp. category will be shown later |
| 2013 | Transcranial sonography in patients with Parkinson's disease with glucocerebrosidase mutations | Kresojević, Nikola | Article | 21M21 |
| 2013 | Transcranial brain parenchyma sonography in Parkinsons disease with glucocerebrosidase Mutations | Mijajlović, Milija | Conference Paper | Mp. category will be shown later |
| 2013 | Pregnancy thrombophilia - the unsuspected risk | Novaković, Ivana V. | Book parts | Mp. category will be shown later |
| 2013 | Transkranijalna sonografija u sporadičnoj formi Krojcfeld-Jakobove bolesti | Nikola Veselinović; Zidverc-Trajković, Jasna | Conference Paper | Mp. category will be shown later |
| 2013 | No Association between Brain-Derived Neurotrophic Factor G196A Polymorphism and Clinical Features of Parkinson's Disease | Svetel, Marina | Article | 22M22 |
| 2013 | Psychosocial risk factors for vulnerability to depression and anxiety | Dujmović, A.; Ignjatović, I.; Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2013 | A novel Notch3 Gly89Cys mutation in a Serbian CADASIL family | Pavlović, Aleksandra | Article | 23M23 |
| 2013 | Distribution of Apolipoprotein E Gene Polymorphism in Students and in High-Educated Elderly from Serbia | Maksimović, Nela | Article | 23M23 |
| 2013 | No major impact of insertion/deletion polymorphism of the angiotensin-converting enzyme gene on susceptibility to rheumatoid arthritis in Serbian patients | Damnjanović, Tatjana M. | Conference Paper | Mp. category will be shown later |
| 2013 | Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification | Hsu, Sandy Chan; Sears, Renee L.; Lemos, Roberta R.; Quintáns, Beatriz; Huang, Alden; Spiteri, Elizabeth; Nevarez, Lisette; Mamah, Catherine; Zatz, Mayana; Pierce, Kerrie D.;
Fullerton, Janice M.; Adair, John C.; Berner, Jon E.; Bower, Matthew; Brodaty, Henry; Carmona, Olga; Dobricić, Valerija; Fogel, Brent L.; García-Estevez, Daniel; Goldman, Jill; Goudreau, John L.; Hopfer, Suellen; Janković, Milena; Jaumà, Serge; Jen, Joanna C.; Kirdlarp, Suppachok; Klepper, Joerg; Kostić, Vladimir; Lang, Anthony E.; Linglart, Agnès; Maisenbacher, Melissa K.; Manyam, Bala V.; Mazzoni, Pietro; Miedzybrodzka, Zofia; Mitarnun, Witoon; Mitchell, Philip B.; Mueller, Jennifer; Novaković, Ivana
| Article | 21M21 |
| 2013 | Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility | Hodžić, Alenka; Ristanović, Momčilo | Article | 21aM21a |
| 2012 | Amplification of cyclin A gene in Wilms tumor | Radojević-Škodrić, Sanja | Conference Paper | Mp. category will be shown later |
| 2012 | The study of association of APOB, APOE and ENOS gene polymorphisms with lipid traits in healthy adolescents![]() | Damnjanović, Tatjana | Conference Paper | Mp. category will be shown later |
| 2012 | Gene polymorphisms associated with thrombophilia in Serbian population![]() | Novaković, Ivana | Conference Paper | Mp. category will be shown later |
| 2012 | A NEW MISSENSE MUTATION WITHIN EXON - 3 OF NOTCH3 GENE IN A STROKE PATIENT | Kozić, Duško | Conference Paper | Mp. category will be shown later |
| 2012 | Ethical principles in pharmacogenetics | Maksimović, Nela | Book parts | Mp. category will be shown later |
| 2012 | Association of dihydrofolate reductase (DHFR)-317AA genotype with poor response to methotrexate in patients with rheumatoid arthritis![]() | Milić, Vera | Article | 22M22 |
