Researchers
Radojković, Dragica
Results 81-100 of 186
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2014 | Učestalost polimorfizma PAI-1 4G/5G kod žena sa spontanim pobačajem - prvi podaci za srpsku populaciju | Đorđević, Valentina | Article | 23M23 |
| 2014 | Molekularne osnove trombofilije | Đorđević, Valentina | Article | 23M23 |
| 2014 | Determination of Transgene Copy Number in Stably Transfected Mammalian Cells by PCR-Capillary Electrophoresis Assay | Pruner, Iva | Article | 23M23 |
| 2014 | Age-dependent influence of ADRB2 gene polymorphisms on asthma severity in Serbian population | Petrović Stanojević, Nataša D. | Conference Paper | Mp. category will be shown later |
| 2014 | Poor pregnancy outcome in women with homozygous type-II HBS antithrombin deficiency | Kovač, Mirjana | Contribution to periodical | 21M21 |
| 2014 | The c20068t gene variant in the 3 ' end of the prothrombin gene is the risk factor for recurrent pregnancy loss | Pruner, Iva | Conference Paper | Mp. category will be shown later |
| 2014 | Is an integrative laboratory algorithm more effective in detecting alpha-1-antitrypsin deficiency in patients with premature chronic obstructive pulmonary disease than AAT concentration based screening approach?![]() | Beletić, Anđelo | Article | 21M21 |
| 2014 | A High Prophylactic LMWH Dose Successfully Suppressed Haemostatic Activity in Pregnant Woman with a New Prothrombin FII G20031T (C.1787G > A) Mutation![]() | Kovač, Mirjana K. | Conference Paper | Mp. category will be shown later |
| 2014 | The 3 ' End Prothrombin Gene Variants in Patients With Different Thrombotic Events | Đorđević, Valentina | Article | 23M23 |
| 2014 | The 3ʼ end prothrombin gene variants in Serbian patients with idiopathic thrombophilia | Arađanski, Marijana; Đorđević, Valentina | Article | 23M23 |
| 2014 | Clinical presentation of mild cystic fibrosis in a Serbian patient homozygous for the CFTR mutation c.1393-1G gt A | Nikolić, Aleksandra | Article | 21M21 |
| 2014 | Risk factors for thrombosis in Serbian children![]() | Šerbić-Nonković, Olivera M. | Article | 23M23 |
| 2014 | NMD SerbNet - integrativni pristup u dijagnostici neuromišićnih bolesti u Srbiji![]() | Milić-Rašić, Vedrana | Article | 52M52 |
| 2014 | Ankrd1-mediated signaling is supported by its interaction with zonula occludens-1 | Nestorović, Aleksandra | Article | 22M22 |
| 2014 | Diagnosis of neuromuscular diseases in Serbia and launch of the Serbian neuromuscular disease network NMD-SERBNET | Kojić, Snežana | Conference Paper | Mp. category will be shown later |
| 2014 | The presence of prothrombotic mutations and a higher FVIII activity contribute to thrombosis development during the breast cancer treatment | Kovač, Mirjana | Conference Paper | Mp. category will be shown later |
| 2014 | Analysis of the SMAD4 gene in asthma | Miletić, Aleksandra; Petrović-Stanojević, Nataša | Article | 23M23 |
| 2013 | Pharmacogenetic tests could be helpful in predicting of VKA maintenance dose in elderly patients at treatment initiation | Kovač, Mirjana | Article | 22M22 |
| 2013 | Analysis of CFTR Gene Variants in Idiopathic Bronchiectasis in Serbian Children![]() | Milosevic, Katarina; Nikolić, Aleksandra | Article | 23M23 |
| 2013 | Genske varijante faktora nekroze tumora-alfa i alfa1antitripsina kod pedijatrijskih pacijenata sa arterijskim ishemijskim moždanim udarom u Srbiji | Đorđević, Valentina | Article | 23M23 |
