Researchers
Radojković, Dragica
Results 81-100 of 186
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 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 |
| 2014 | Does anticoagulant therapy improve pregnancy outcome equally, regardless of specific thrombophilia type?![]() | Kovač, Mirjana | Article | 22M22 |
| 2014 | The 3 ' End Prothrombin Gene Variants in Patients With Different Thrombotic Events | Đorđević, Valentina | Article | 23M23 |
| 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 | 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 | The 3ʼ end prothrombin gene variants in Serbian patients with idiopathic thrombophilia | Arađanski, Marijana; Đorđević, Valentina | Article | 23M23 |
| 2014 | Clinical characteristics of first venous thrombosis among women under and over 45 years of age![]() | Kovač, Mirjana | Article | 24M24 |
| 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 | 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 | Poor pregnancy outcome in women with homozygous type-II HBS antithrombin deficiency | Kovač, Mirjana | Contribution to periodical | 21M21 |
| 2014 | NMD SerbNet - integrativni pristup u dijagnostici neuromišićnih bolesti u Srbiji![]() | Milić-Rašić, Vedrana | Article | 52M52 |
| 2014 | Risk factors for thrombosis in Serbian children![]() | Šerbić-Nonković, Olivera M. | Article | 23M23 |
| 2014 | Učestalost polimorfizma PAI-1 4G/5G kod žena sa spontanim pobačajem - prvi podaci za srpsku populaciju | Đorđević, Valentina | Article | 23M23 |
| 2014 | Alpha-1-antitrypsin deficiency: Molecular basis, clinical presentation, therapeutic options and an integrative approach in diagnostics![]() | Beletić, Anđelo | Article | 23M23 |
| 2014 | Functional analysis of novel alpha-1 antitrypsin variants G320R and V321F | Ljujić, Mila | Article | 22M22 |
| 2014 | Polymorphisms of Beta2-Adrenergic Receptor Gene in Serbian Asthmatic Adults: Effects on Response to Beta-Agonists | Petrović-Stanojević, Nataša | Article | 22M22 |
| 2013 | Gender-related reference intervals of urinary 8-oxo-7,8-dihydro-2 '-deoxyguanosine determined by liquid chromatography-tandem mass spectrometry in Serbian population | Topić, Aleksandra | Article | 21M21 |
| 2013 | Učestalost alela CCR5Δ32 u srpskoj populaciji | Đorđević, Valentina | Article | 23M23 |
| 2013 | Rationalized DNA sequencing-based protocol for genotyping patients receiving coumarin therapy | Rakićević, Ljiljana | Article | 22M22 |
