TY  - CONF
AU  - Miković, D.
AU  - Janković, G.
AU  - Rakić, L.
AU  - Dolni-Car, M. Benedikt
AU  - Debeljak, M.
AU  - Rakićević, Ljiljana
AU  - Plecas, D.
PY  - 2012
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/560
PB  - Wiley-Blackwell, Hoboken
C3  - Haemophilia
T1  - Prenatal diagnosis of hemophilia in Serbia: Evolution from phenotypic to molecular methods
EP  - 159
SP  - 159
VL  - 18
UR  - https://hdl.handle.net/21.15107/rcub_imagine_560
ER  - 

@conference{
author = "Miković, D. and Janković, G. and Rakić, L. and Dolni-Car, M. Benedikt and Debeljak, M. and Rakićević, Ljiljana and Plecas, D.",
year = "2012",
publisher = "Wiley-Blackwell, Hoboken",
journal = "Haemophilia",
title = "Prenatal diagnosis of hemophilia in Serbia: Evolution from phenotypic to molecular methods",
pages = "159-159",
volume = "18",
url = "https://hdl.handle.net/21.15107/rcub_imagine_560"
}

Miković, D., Janković, G., Rakić, L., Dolni-Car, M. B., Debeljak, M., Rakićević, L.,& Plecas, D.. (2012). Prenatal diagnosis of hemophilia in Serbia: Evolution from phenotypic to molecular methods. in Haemophilia
Wiley-Blackwell, Hoboken., 18, 159-159.
https://hdl.handle.net/21.15107/rcub_imagine_560

Miković D, Janković G, Rakić L, Dolni-Car MB, Debeljak M, Rakićević L, Plecas D. Prenatal diagnosis of hemophilia in Serbia: Evolution from phenotypic to molecular methods. in Haemophilia. 2012;18:159-159.
https://hdl.handle.net/21.15107/rcub_imagine_560 .

Miković, D., Janković, G., Rakić, L., Dolni-Car, M. Benedikt, Debeljak, M., Rakićević, Ljiljana, Plecas, D., "Prenatal diagnosis of hemophilia in Serbia: Evolution from phenotypic to molecular methods" in Haemophilia, 18 (2012):159-159,
https://hdl.handle.net/21.15107/rcub_imagine_560 .

TY  - CONF
AU  - Miković, D.
AU  - Janković, G.
AU  - Rakić, L.
AU  - Plecas, D.
AU  - Rakićević, Ljiljana
AU  - Kovač, Mirjana
PY  - 2008
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/303
PB  - Wiley-Blackwell, Malden
C3  - Haemophilia
T1  - Prenatal diagnosis of hemophlia in Serbia - twenty years experience
EP  - 6
SP  - 6
VL  - 14
UR  - https://hdl.handle.net/21.15107/rcub_imagine_303
ER  - 

@conference{
author = "Miković, D. and Janković, G. and Rakić, L. and Plecas, D. and Rakićević, Ljiljana and Kovač, Mirjana",
year = "2008",
publisher = "Wiley-Blackwell, Malden",
journal = "Haemophilia",
title = "Prenatal diagnosis of hemophlia in Serbia - twenty years experience",
pages = "6-6",
volume = "14",
url = "https://hdl.handle.net/21.15107/rcub_imagine_303"
}

Miković, D., Janković, G., Rakić, L., Plecas, D., Rakićević, L.,& Kovač, M.. (2008). Prenatal diagnosis of hemophlia in Serbia - twenty years experience. in Haemophilia
Wiley-Blackwell, Malden., 14, 6-6.
https://hdl.handle.net/21.15107/rcub_imagine_303

Miković D, Janković G, Rakić L, Plecas D, Rakićević L, Kovač M. Prenatal diagnosis of hemophlia in Serbia - twenty years experience. in Haemophilia. 2008;14:6-6.
https://hdl.handle.net/21.15107/rcub_imagine_303 .

Miković, D., Janković, G., Rakić, L., Plecas, D., Rakićević, Ljiljana, Kovač, Mirjana, "Prenatal diagnosis of hemophlia in Serbia - twenty years experience" in Haemophilia, 14 (2008):6-6,
https://hdl.handle.net/21.15107/rcub_imagine_303 .

TY  - JOUR
AU  - Stanković, Marija
AU  - Rakićević, Ljiljana
AU  - Miković, D.
AU  - Janković, G.
PY  - 2005
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/229
AB  - Haemophilia B is the third most common bleeding disorder, affecting 1:30000 males, caused by the deficiency or dysfunction of the coagulation factor IX (FIX). The mutations causing abnormal FIX are very numerous and heterogeneous, which greatly hinders direct mutation detection. Indirect diagnostics based on polymorphic DNA markers is the most widely used approach for carrier detection and prenatal diagnosis in families at risk. Three RFLPs (Xmnl, TaqI and Hhal), as well as microsatellite polymorphism Ddel in eight haemophilia B families were analyzed. Allelic frequencies and heterozygosity rate for each polymorphism were determined. The carrier status and feasibility of prenatal diagnosis of haemophilia B using DNA markers in these families were also studied. Our results showed that 87.5% families were informative for at least one polymorphic DNA marker. These results enable prenatal diagnosis in future pregnancies for informative families. This study also provided the first data regarding FIX polymorphisms and their allelic frequencies in Serbian population.
PB  - Institut za transfuziju krvi Srbije, Beograd
T2  - Bilten za transfuziologiju
T1  - Molecular diagnostics of haemophilia B using polymorphic DNA markers in Serbian population
EP  - 19
IS  - 1-2
SP  - 16
VL  - 51
UR  - https://hdl.handle.net/21.15107/rcub_imagine_229
ER  - 

@article{
author = "Stanković, Marija and Rakićević, Ljiljana and Miković, D. and Janković, G.",
year = "2005",
abstract = "Haemophilia B is the third most common bleeding disorder, affecting 1:30000 males, caused by the deficiency or dysfunction of the coagulation factor IX (FIX). The mutations causing abnormal FIX are very numerous and heterogeneous, which greatly hinders direct mutation detection. Indirect diagnostics based on polymorphic DNA markers is the most widely used approach for carrier detection and prenatal diagnosis in families at risk. Three RFLPs (Xmnl, TaqI and Hhal), as well as microsatellite polymorphism Ddel in eight haemophilia B families were analyzed. Allelic frequencies and heterozygosity rate for each polymorphism were determined. The carrier status and feasibility of prenatal diagnosis of haemophilia B using DNA markers in these families were also studied. Our results showed that 87.5% families were informative for at least one polymorphic DNA marker. These results enable prenatal diagnosis in future pregnancies for informative families. This study also provided the first data regarding FIX polymorphisms and their allelic frequencies in Serbian population.",
publisher = "Institut za transfuziju krvi Srbije, Beograd",
journal = "Bilten za transfuziologiju",
title = "Molecular diagnostics of haemophilia B using polymorphic DNA markers in Serbian population",
pages = "19-16",
number = "1-2",
volume = "51",
url = "https://hdl.handle.net/21.15107/rcub_imagine_229"
}

Stanković, M., Rakićević, L., Miković, D.,& Janković, G.. (2005). Molecular diagnostics of haemophilia B using polymorphic DNA markers in Serbian population. in Bilten za transfuziologiju
Institut za transfuziju krvi Srbije, Beograd., 51(1-2), 16-19.
https://hdl.handle.net/21.15107/rcub_imagine_229

Stanković M, Rakićević L, Miković D, Janković G. Molecular diagnostics of haemophilia B using polymorphic DNA markers in Serbian population. in Bilten za transfuziologiju. 2005;51(1-2):16-19.
https://hdl.handle.net/21.15107/rcub_imagine_229 .

Stanković, Marija, Rakićević, Ljiljana, Miković, D., Janković, G., "Molecular diagnostics of haemophilia B using polymorphic DNA markers in Serbian population" in Bilten za transfuziologiju, 51, no. 1-2 (2005):16-19,
https://hdl.handle.net/21.15107/rcub_imagine_229 .

TY  - JOUR
AU  - Antonijević, Nebojša
AU  - Stanojević, M
AU  - Milosević, R
AU  - Đorđević, Valentina
AU  - Jauković, M
AU  - Vukcević, V
AU  - Kovač, Mirjana
AU  - Miković, D
AU  - Radojković, Dragica
AU  - Vasiljević, Z
PY  - 2005
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/217
AB  - We present the case of a 64 year-old female patient, with a clearly positive family history of venous thromboembolism (VTE), multiple VTE episodes (massive pulmonary embolism, ovarian venous plexus thrombosis, deep venous thrombosis with submassive pulmonary embolism and second deep venous thrombosis) and myocardial infarction. Laboratory tests revealed the resistance to the activated protein C, elevated FVIII and PAI-1. The patient was found to be a heterozygous carrier of FV Leiden, MTHFR C677T and PAI-1 4G/5G mutations. She was diagnosed with essential thrombocythemia at the age of 60. The thirty-three-year follow-up of our patient and detection of recurrent thrombotic episodes in the light of multiple coagulation defects with proved acquired risk factors, contributes to the risk stratification in the group of patients with very high risk. In case of our patient, we stress inadequacy of widely-accepted standard prevention measures. In our opinion, patients with very high risk require additional mechanic and specific medicament methods of VTE prevention.
PB  - Springer, Dordrecht
T2  - Journal of Thrombosis and Thrombolysis
T1  - Combined thrombophilic risk factors and essential thrombocythemia in patient with recurrent venous thromboembolic episodes - Thirty-three-year follow-up
EP  - 95
IS  - 2
SP  - 93
VL  - 19
DO  - 10.1007/s11239-005-0783-1
ER  - 

@article{
author = "Antonijević, Nebojša and Stanojević, M and Milosević, R and Đorđević, Valentina and Jauković, M and Vukcević, V and Kovač, Mirjana and Miković, D and Radojković, Dragica and Vasiljević, Z",
year = "2005",
abstract = "We present the case of a 64 year-old female patient, with a clearly positive family history of venous thromboembolism (VTE), multiple VTE episodes (massive pulmonary embolism, ovarian venous plexus thrombosis, deep venous thrombosis with submassive pulmonary embolism and second deep venous thrombosis) and myocardial infarction. Laboratory tests revealed the resistance to the activated protein C, elevated FVIII and PAI-1. The patient was found to be a heterozygous carrier of FV Leiden, MTHFR C677T and PAI-1 4G/5G mutations. She was diagnosed with essential thrombocythemia at the age of 60. The thirty-three-year follow-up of our patient and detection of recurrent thrombotic episodes in the light of multiple coagulation defects with proved acquired risk factors, contributes to the risk stratification in the group of patients with very high risk. In case of our patient, we stress inadequacy of widely-accepted standard prevention measures. In our opinion, patients with very high risk require additional mechanic and specific medicament methods of VTE prevention.",
publisher = "Springer, Dordrecht",
journal = "Journal of Thrombosis and Thrombolysis",
title = "Combined thrombophilic risk factors and essential thrombocythemia in patient with recurrent venous thromboembolic episodes - Thirty-three-year follow-up",
pages = "95-93",
number = "2",
volume = "19",
doi = "10.1007/s11239-005-0783-1"
}

Antonijević, N., Stanojević, M., Milosević, R., Đorđević, V., Jauković, M., Vukcević, V., Kovač, M., Miković, D., Radojković, D.,& Vasiljević, Z.. (2005). Combined thrombophilic risk factors and essential thrombocythemia in patient with recurrent venous thromboembolic episodes - Thirty-three-year follow-up. in Journal of Thrombosis and Thrombolysis
Springer, Dordrecht., 19(2), 93-95.
https://doi.org/10.1007/s11239-005-0783-1

Antonijević N, Stanojević M, Milosević R, Đorđević V, Jauković M, Vukcević V, Kovač M, Miković D, Radojković D, Vasiljević Z. Combined thrombophilic risk factors and essential thrombocythemia in patient with recurrent venous thromboembolic episodes - Thirty-three-year follow-up. in Journal of Thrombosis and Thrombolysis. 2005;19(2):93-95.
doi:10.1007/s11239-005-0783-1 .

Antonijević, Nebojša, Stanojević, M, Milosević, R, Đorđević, Valentina, Jauković, M, Vukcević, V, Kovač, Mirjana, Miković, D, Radojković, Dragica, Vasiljević, Z, "Combined thrombophilic risk factors and essential thrombocythemia in patient with recurrent venous thromboembolic episodes - Thirty-three-year follow-up" in Journal of Thrombosis and Thrombolysis, 19, no. 2 (2005):93-95,
https://doi.org/10.1007/s11239-005-0783-1 . .

TY  - JOUR
AU  - Stanković, Marija
AU  - Rakićević, Ljiljana
AU  - Miković, D
AU  - Janković, G
AU  - Nikolić, Aleksandra
PY  - 2005
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/228
PB  - Wiley, Hoboken
T2  - Clinical and Laboratory Haematology
T1  - Indirect diagnosis of haemophilia B by multiplex PCR/RFLP
EP  - 146
IS  - 2
SP  - 145
VL  - 27
DO  - 10.1111/j.1365-2257.2005.00671.x
ER  - 

@article{
author = "Stanković, Marija and Rakićević, Ljiljana and Miković, D and Janković, G and Nikolić, Aleksandra",
year = "2005",
publisher = "Wiley, Hoboken",
journal = "Clinical and Laboratory Haematology",
title = "Indirect diagnosis of haemophilia B by multiplex PCR/RFLP",
pages = "146-145",
number = "2",
volume = "27",
doi = "10.1111/j.1365-2257.2005.00671.x"
}

Stanković, M., Rakićević, L., Miković, D., Janković, G.,& Nikolić, A.. (2005). Indirect diagnosis of haemophilia B by multiplex PCR/RFLP. in Clinical and Laboratory Haematology
Wiley, Hoboken., 27(2), 145-146.
https://doi.org/10.1111/j.1365-2257.2005.00671.x

Stanković M, Rakićević L, Miković D, Janković G, Nikolić A. Indirect diagnosis of haemophilia B by multiplex PCR/RFLP. in Clinical and Laboratory Haematology. 2005;27(2):145-146.
doi:10.1111/j.1365-2257.2005.00671.x .

Stanković, Marija, Rakićević, Ljiljana, Miković, D, Janković, G, Nikolić, Aleksandra, "Indirect diagnosis of haemophilia B by multiplex PCR/RFLP" in Clinical and Laboratory Haematology, 27, no. 2 (2005):145-146,
https://doi.org/10.1111/j.1365-2257.2005.00671.x . .

TY  - JOUR
AU  - Đorđević, Valentina
AU  - Rakićević, Ljiljana
AU  - Miković, D
AU  - Kovač, Mirjana
AU  - Miljić, Predrag
PY  - 2004
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/202
PB  - Karger, Basel
T2  - Acta Haematologica
T1  - Prevalence of factor V Leiden, factor V Cambridge, factor II G20210A and methylenetetrahydrofolate reductase C677T mutations in healthy and thrombophilic Serbian populations
EP  - 229
IS  - 4
SP  - 227
VL  - 112
DO  - 10.1159/000081280
ER  - 

@article{
author = "Đorđević, Valentina and Rakićević, Ljiljana and Miković, D and Kovač, Mirjana and Miljić, Predrag",
year = "2004",
publisher = "Karger, Basel",
journal = "Acta Haematologica",
title = "Prevalence of factor V Leiden, factor V Cambridge, factor II G20210A and methylenetetrahydrofolate reductase C677T mutations in healthy and thrombophilic Serbian populations",
pages = "229-227",
number = "4",
volume = "112",
doi = "10.1159/000081280"
}

Đorđević, V., Rakićević, L., Miković, D., Kovač, M.,& Miljić, P.. (2004). Prevalence of factor V Leiden, factor V Cambridge, factor II G20210A and methylenetetrahydrofolate reductase C677T mutations in healthy and thrombophilic Serbian populations. in Acta Haematologica
Karger, Basel., 112(4), 227-229.
https://doi.org/10.1159/000081280

Đorđević V, Rakićević L, Miković D, Kovač M, Miljić P. Prevalence of factor V Leiden, factor V Cambridge, factor II G20210A and methylenetetrahydrofolate reductase C677T mutations in healthy and thrombophilic Serbian populations. in Acta Haematologica. 2004;112(4):227-229.
doi:10.1159/000081280 .

Đorđević, Valentina, Rakićević, Ljiljana, Miković, D, Kovač, Mirjana, Miljić, Predrag, "Prevalence of factor V Leiden, factor V Cambridge, factor II G20210A and methylenetetrahydrofolate reductase C677T mutations in healthy and thrombophilic Serbian populations" in Acta Haematologica, 112, no. 4 (2004):227-229,
https://doi.org/10.1159/000081280 . .

TY  - JOUR
AU  - Miković, D
AU  - Rakićević, Ljiljana
AU  - Kovač, Mirjana
AU  - Radojković, Dragica
PY  - 2000
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/141
PB  - Georg Thieme Verlag Kg, Stuttgart
T2  - Thrombosis and Haemostasis
T1  - Prevalence of factor V Leiden mutation in Yugoslav thrombophilic patients and its relationship to the laboratory diagnosis of APC resistance
EP  - 724
IS  - 4
SP  - 723
VL  - 84
UR  - https://hdl.handle.net/21.15107/rcub_imagine_141
ER  - 

@article{
author = "Miković, D and Rakićević, Ljiljana and Kovač, Mirjana and Radojković, Dragica",
year = "2000",
publisher = "Georg Thieme Verlag Kg, Stuttgart",
journal = "Thrombosis and Haemostasis",
title = "Prevalence of factor V Leiden mutation in Yugoslav thrombophilic patients and its relationship to the laboratory diagnosis of APC resistance",
pages = "724-723",
number = "4",
volume = "84",
url = "https://hdl.handle.net/21.15107/rcub_imagine_141"
}

Miković, D., Rakićević, L., Kovač, M.,& Radojković, D.. (2000). Prevalence of factor V Leiden mutation in Yugoslav thrombophilic patients and its relationship to the laboratory diagnosis of APC resistance. in Thrombosis and Haemostasis
Georg Thieme Verlag Kg, Stuttgart., 84(4), 723-724.
https://hdl.handle.net/21.15107/rcub_imagine_141

Miković D, Rakićević L, Kovač M, Radojković D. Prevalence of factor V Leiden mutation in Yugoslav thrombophilic patients and its relationship to the laboratory diagnosis of APC resistance. in Thrombosis and Haemostasis. 2000;84(4):723-724.
https://hdl.handle.net/21.15107/rcub_imagine_141 .

Miković, D, Rakićević, Ljiljana, Kovač, Mirjana, Radojković, Dragica, "Prevalence of factor V Leiden mutation in Yugoslav thrombophilic patients and its relationship to the laboratory diagnosis of APC resistance" in Thrombosis and Haemostasis, 84, no. 4 (2000):723-724,
https://hdl.handle.net/21.15107/rcub_imagine_141 .