Istraživači
Rakićević, Ljiljana
Date issued
Results 41-60 of 68
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2010 | The use of D-dimer with new cutoff can be useful in diagnosis of venous thromboembolism in pregnancy | Kovač, Mirjana | Article | 22M22 |
| 2010 | The c.-1639G gt A polymorphism of the VKORC1 gene in Serbian population: retrospective study of the variability in response to oral anticoagulant therapy | Kovač, Mirjana | Article | 22M22 |
| 2010 | +1040 C/T polymorphism in coding region of thrombin-activatable fibrinolysis inhibitor gene and the risk of idiopathic recurrent fetal loss | Pruner, Iva | Article | 22M22 |
| 2010 | A novel role for cardiac ankyrin repeat protein Ankrd1/CARP as a co-activator of the p53 tumor suppressor protein | Kojić, Snežana | Article | 22M22 |
| 2010 | Type and Location of Venous Thromboembolism in Carriers of Factor V Leiden or Prothrombin G20210A Mutation Versus Patients With No Mutation | Kovač, Mirjana | Article | 22M22 |
| 2010 | Funkcionalna analiza proteina hAnkrd2: regulacija ekspresije i aktivnosti![]() | Rakićević, Ljiljana | Doctoral theses | 70M70 |
| 2010 | Thrombophilia in Women with Pregnancy-Associated Complications: Fetal Loss and Pregnancy-Related Venous Thromboembolism | Kovač, Mirjana | Article | 22M22 |
| 2009 | Genetic Risk Factors for Arterial Ischemic Stroke in Children: A Possible MTHFR and eNOS Gene-Gene Interplay? | Đorđević, Valentina | Article | 22M22 |
| 2009 | The use of D-dimer with new threshold in diagnosis of venous thromboembolism in pregnancy | Kovač, Mirjana | Conference Paper | Mp. category will be shown later |
| 2009 | Matrix Metalloproteinases Gene Variants in Idiopathic Disseminated Bronchiectasis![]() | Stanković, Marija | Article | 21M21 |
| 2009 | Uticaj polimorfizma c.-1639g gt A VKORC1 gena na terapijski odgovor u toku primene oralnih antikoagulanasa | Kovač, Mirjana | Article | 24M24 |
| 2008 | FV Leiden mutation and risk of recurrent venous thromboembolism in Serbian population | Kovač, Mirjana | Article | 22M22 |
| 2008 | Prenatal diagnosis of hemophlia in Serbia - twenty years experience | Miković, D.; Janković, G.; Rakić, L. | Conference Paper | Mp. category will be shown later |
| 2007 | Polymorphism MTHFR C677T in patients with chronic pancreatitis and pancreatic cancer![]() | Nikolić, A. | Conference Paper | Mp. category will be shown later |
| 2006 | PCR amplification on whole blood samples treated with different commonly used anticoagulants | Đorđević, V. | Article | 23M23 |
| 2005 | Pregnancy loss and thrombotic complications during pregnancy and puerperium in women with coinheritance of factor V Leiden and FII G20210A mutation | Miljić, Predrag; Đorđević, V | Conference Paper | Mp. category will be shown later |
| 2005 | Impact of acquired and genetic factors on thrombophilic phenotype in FV leiden mutation carriers | Đorđević, Valentina | Article | Mp. category will be shown later |
| 2005 | Indirect diagnosis of haemophilia B by multiplex PCR/RFLP | Stanković, Marija | Contribution to periodical | 23M23 |
| 2005 | Molecular diagnostics of haemophilia B using polymorphic DNA markers in Serbian population | Stanković, Marija | Article | Mp. category will be shown later |
| 2005 | Mutacije FV Leiden, FII G20210A i MTHFR C677T kao faktori rizika za nastanak tromboze dubokih vena u toku trudnoće ili puerperijuma | Đorđević, Valentina | Article | Mp. category will be shown later |
