Radak, Sandra

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  • Radak, Sandra (6)
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Author's Bibliography

Carotid Restenosis Rate After Stenting for Primary Lesions Versus Restenosis After Endarterectomy With Creation of Risk Index

Tanasković, Slobodan; Sagić, Dragan Ž.; Radak, Đorđe J.; Antonić, Želimir; Kovačević, Vladimir; Vuković, Mira; Aleksić, Nikola; Radak, Sandra; Nenezić, Dragoslav; Cvetković, Slobodan M.; Isenović, Esma R.; Vučurević, Goran; Lozuk, Branko; Babić, Aleksandar; Babić, Srđan; Matić, Predrag; Gajin, Predrag; Unić-Stojanović, Dragana; Ilijevski, Nenad

(2022)

TY  - JOUR
AU  - Tanasković, Slobodan
AU  - Sagić, Dragan Ž.
AU  - Radak, Đorđe J.
AU  - Antonić, Želimir
AU  - Kovačević, Vladimir
AU  - Vuković, Mira
AU  - Aleksić, Nikola
AU  - Radak, Sandra
AU  - Nenezić, Dragoslav
AU  - Cvetković, Slobodan M.
AU  - Isenović, Esma R.
AU  - Vučurević, Goran
AU  - Lozuk, Branko
AU  - Babić, Aleksandar
AU  - Babić, Srđan
AU  - Matić, Predrag
AU  - Gajin, Predrag
AU  - Unić-Stojanović, Dragana
AU  - Ilijevski, Nenad
PY  - 2022
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10259
AB  - Purpose: Carotid artery stenting (CAS) is an option for carotid restenosis (CR) treatment with favorable outcomes. However, CAS has also emerged as an alternative to carotid endarterectomy (CEA) for the management of patients with primary carotid stenosis. This study aimed to report CR rates after CAS was performed in patients with primary lesions versus restenosis after CEA, to identify predictors of CR, and to report both neurological and overall outcomes.Materials and methods:From January 2000 to September 2018, a total of 782 patients were divided into 2 groups: The CAS (prim) group consisted of 440 patients in whom CAS was performed for primary lesions, and the CAS (res) group consisted of 342 patients with CAS due to restenosis after CEA. Indications for CAS were symptomatic stenosis/restenosis >70% and asymptomatic stenosis/restenosis >85%. A color duplex scan (CDS) of carotid arteries was performed 6 months after CAS, after 1 year, and annually afterward. Follow-up ranged from 12 to 88 months, with a mean follow-up of 34.6±18.0 months.Results:There were no differences in terms of CR rate between the patients in the CAS (prim) and CAS (res) groups (8.7% vs 7.2%, ?2=0.691, p=0.406). The overall CR rate was 7.9%, whereas significant CR (>70%) rate needing re-intervention was 5.6%, but there was no difference between patients in the CAS (prim) and CAS (res) groups (6.4% vs 4.7%, p=0.351). Six independent predictors for CR were smoking, associated previous myocardial infarction and angina pectoris, plaque morphology, spasm after CAS, the use of FilterWire or Spider Fx cerebral protection devices, and time after stenting. A carotid restenosis risk index (CRRI) was created based on these predictors and ranged from ?7 (minimal risk) to +10 (maximum risk); patients with a score >?4 were at increased risk for CR. There were no differences in terms of neurological and overall morbidity and mortality between the 2 groups.Conclusions:There was no difference in CR rate after CAS between the patients with primary stenosis and restenosis after CEA. A CRRI score >?4 is a criterion for identifying high-risk patients for post-CAS CR that should be tested in future randomized trials.
T2  - Journal of Endovascular Therapy
T1  - Carotid Restenosis Rate After Stenting for Primary Lesions Versus Restenosis After Endarterectomy With Creation of Risk Index
SP  - 15266028221091895
DO  - 10.1177/15266028221091895
ER  - 
@article{
author = "Tanasković, Slobodan and Sagić, Dragan Ž. and Radak, Đorđe J. and Antonić, Želimir and Kovačević, Vladimir and Vuković, Mira and Aleksić, Nikola and Radak, Sandra and Nenezić, Dragoslav and Cvetković, Slobodan M. and Isenović, Esma R. and Vučurević, Goran and Lozuk, Branko and Babić, Aleksandar and Babić, Srđan and Matić, Predrag and Gajin, Predrag and Unić-Stojanović, Dragana and Ilijevski, Nenad",
year = "2022",
abstract = "Purpose: Carotid artery stenting (CAS) is an option for carotid restenosis (CR) treatment with favorable outcomes. However, CAS has also emerged as an alternative to carotid endarterectomy (CEA) for the management of patients with primary carotid stenosis. This study aimed to report CR rates after CAS was performed in patients with primary lesions versus restenosis after CEA, to identify predictors of CR, and to report both neurological and overall outcomes.Materials and methods:From January 2000 to September 2018, a total of 782 patients were divided into 2 groups: The CAS (prim) group consisted of 440 patients in whom CAS was performed for primary lesions, and the CAS (res) group consisted of 342 patients with CAS due to restenosis after CEA. Indications for CAS were symptomatic stenosis/restenosis >70% and asymptomatic stenosis/restenosis >85%. A color duplex scan (CDS) of carotid arteries was performed 6 months after CAS, after 1 year, and annually afterward. Follow-up ranged from 12 to 88 months, with a mean follow-up of 34.6±18.0 months.Results:There were no differences in terms of CR rate between the patients in the CAS (prim) and CAS (res) groups (8.7% vs 7.2%, ?2=0.691, p=0.406). The overall CR rate was 7.9%, whereas significant CR (>70%) rate needing re-intervention was 5.6%, but there was no difference between patients in the CAS (prim) and CAS (res) groups (6.4% vs 4.7%, p=0.351). Six independent predictors for CR were smoking, associated previous myocardial infarction and angina pectoris, plaque morphology, spasm after CAS, the use of FilterWire or Spider Fx cerebral protection devices, and time after stenting. A carotid restenosis risk index (CRRI) was created based on these predictors and ranged from ?7 (minimal risk) to +10 (maximum risk); patients with a score >?4 were at increased risk for CR. There were no differences in terms of neurological and overall morbidity and mortality between the 2 groups.Conclusions:There was no difference in CR rate after CAS between the patients with primary stenosis and restenosis after CEA. A CRRI score >?4 is a criterion for identifying high-risk patients for post-CAS CR that should be tested in future randomized trials.",
journal = "Journal of Endovascular Therapy",
title = "Carotid Restenosis Rate After Stenting for Primary Lesions Versus Restenosis After Endarterectomy With Creation of Risk Index",
pages = "15266028221091895",
doi = "10.1177/15266028221091895"
}
Tanasković, S., Sagić, D. Ž., Radak, Đ. J., Antonić, Ž., Kovačević, V., Vuković, M., Aleksić, N., Radak, S., Nenezić, D., Cvetković, S. M., Isenović, E. R., Vučurević, G., Lozuk, B., Babić, A., Babić, S., Matić, P., Gajin, P., Unić-Stojanović, D.,& Ilijevski, N.. (2022). Carotid Restenosis Rate After Stenting for Primary Lesions Versus Restenosis After Endarterectomy With Creation of Risk Index. in Journal of Endovascular Therapy, 15266028221091895.
https://doi.org/10.1177/15266028221091895
Tanasković S, Sagić DŽ, Radak ĐJ, Antonić Ž, Kovačević V, Vuković M, Aleksić N, Radak S, Nenezić D, Cvetković SM, Isenović ER, Vučurević G, Lozuk B, Babić A, Babić S, Matić P, Gajin P, Unić-Stojanović D, Ilijevski N. Carotid Restenosis Rate After Stenting for Primary Lesions Versus Restenosis After Endarterectomy With Creation of Risk Index. in Journal of Endovascular Therapy. 2022;:15266028221091895.
doi:10.1177/15266028221091895 .
Tanasković, Slobodan, Sagić, Dragan Ž., Radak, Đorđe J., Antonić, Želimir, Kovačević, Vladimir, Vuković, Mira, Aleksić, Nikola, Radak, Sandra, Nenezić, Dragoslav, Cvetković, Slobodan M., Isenović, Esma R., Vučurević, Goran, Lozuk, Branko, Babić, Aleksandar, Babić, Srđan, Matić, Predrag, Gajin, Predrag, Unić-Stojanović, Dragana, Ilijevski, Nenad, "Carotid Restenosis Rate After Stenting for Primary Lesions Versus Restenosis After Endarterectomy With Creation of Risk Index" in Journal of Endovascular Therapy (2022):15266028221091895,
https://doi.org/10.1177/15266028221091895 . .
1

The sex-specific association of Met62Ile gene polymorphism in P-selectin glycoprotein ligand (PSGL-1) with carotid plaque presence: preliminary study

Živković, Maja; Kolaković, Ana; Radak, Đorđe J.; Dinčić, Dragan; Radak, Sandra; Đurić, Tamara; Stanković, Aleksandra

(2012)

TY  - JOUR
AU  - Živković, Maja
AU  - Kolaković, Ana
AU  - Radak, Đorđe J.
AU  - Dinčić, Dragan
AU  - Radak, Sandra
AU  - Đurić, Tamara
AU  - Stanković, Aleksandra
PY  - 2012
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/4823
AB  - Atherosclerosis is known as an inflammatory disease in which a recruitment of leukocytes to the endothelium wall represents a preliminary step of the initiation and the development of disease. The P-selectin glycoprotein ligand (PSGL-1) seems to be the major molecule mediating leukocyte-endothelium interactions and leukocyte rolling on stimulated endothelium. There are limited number of studies reporting on association of Met62Ile SNP in PSGL-1 gene and the risk for atherosclerosis. The aim of this study was to analyze possible association of this polymorphism with an advanced carotid atherosclerosis and biochemical markers of inflammation and haemostasis. The 275 patients consecutively admitted for carotid endarterectomy with stenosis GT 70% and 256 controls of the same ethnic origin were included in the study. The Met62Ile genotypes were determined by PCR RFLP. The Ile/Ile homozygotes had significantly higher CRP compared to the other genotypes in patients. Female patients had Ile allele dose-dependent association with the carotid plaque presence (Met/Met vs. Met/Ile vs. Ile/Ile; OR 1, OR 2.02, CI 1.0-4.08, OR 4.08, CI 1.0-16.81, respectively, p = 0.04). Our results suggest the impact of PSGL-1 Met62Ile polymorphism on inflammation in advanced atherosclerosis. We observed the sex-differential association of Met62Ile with advanced carotid atherosclerosis. Studies in larger and different populations should validate and further examine the suggested role of genetic variations in PSGL-1 with atherosclerosis and thrombosis.
T2  - Molecular Biology Reports
T1  - The sex-specific association of Met62Ile gene polymorphism in P-selectin glycoprotein ligand (PSGL-1) with carotid plaque presence: preliminary study
VL  - 39
IS  - 6
SP  - 6479
EP  - 6485
DO  - 10.1007/s11033-012-1475-5
ER  - 
@article{
author = "Živković, Maja and Kolaković, Ana and Radak, Đorđe J. and Dinčić, Dragan and Radak, Sandra and Đurić, Tamara and Stanković, Aleksandra",
year = "2012",
abstract = "Atherosclerosis is known as an inflammatory disease in which a recruitment of leukocytes to the endothelium wall represents a preliminary step of the initiation and the development of disease. The P-selectin glycoprotein ligand (PSGL-1) seems to be the major molecule mediating leukocyte-endothelium interactions and leukocyte rolling on stimulated endothelium. There are limited number of studies reporting on association of Met62Ile SNP in PSGL-1 gene and the risk for atherosclerosis. The aim of this study was to analyze possible association of this polymorphism with an advanced carotid atherosclerosis and biochemical markers of inflammation and haemostasis. The 275 patients consecutively admitted for carotid endarterectomy with stenosis GT 70% and 256 controls of the same ethnic origin were included in the study. The Met62Ile genotypes were determined by PCR RFLP. The Ile/Ile homozygotes had significantly higher CRP compared to the other genotypes in patients. Female patients had Ile allele dose-dependent association with the carotid plaque presence (Met/Met vs. Met/Ile vs. Ile/Ile; OR 1, OR 2.02, CI 1.0-4.08, OR 4.08, CI 1.0-16.81, respectively, p = 0.04). Our results suggest the impact of PSGL-1 Met62Ile polymorphism on inflammation in advanced atherosclerosis. We observed the sex-differential association of Met62Ile with advanced carotid atherosclerosis. Studies in larger and different populations should validate and further examine the suggested role of genetic variations in PSGL-1 with atherosclerosis and thrombosis.",
journal = "Molecular Biology Reports",
title = "The sex-specific association of Met62Ile gene polymorphism in P-selectin glycoprotein ligand (PSGL-1) with carotid plaque presence: preliminary study",
volume = "39",
number = "6",
pages = "6479-6485",
doi = "10.1007/s11033-012-1475-5"
}
Živković, M., Kolaković, A., Radak, Đ. J., Dinčić, D., Radak, S., Đurić, T.,& Stanković, A.. (2012). The sex-specific association of Met62Ile gene polymorphism in P-selectin glycoprotein ligand (PSGL-1) with carotid plaque presence: preliminary study. in Molecular Biology Reports, 39(6), 6479-6485.
https://doi.org/10.1007/s11033-012-1475-5
Živković M, Kolaković A, Radak ĐJ, Dinčić D, Radak S, Đurić T, Stanković A. The sex-specific association of Met62Ile gene polymorphism in P-selectin glycoprotein ligand (PSGL-1) with carotid plaque presence: preliminary study. in Molecular Biology Reports. 2012;39(6):6479-6485.
doi:10.1007/s11033-012-1475-5 .
Živković, Maja, Kolaković, Ana, Radak, Đorđe J., Dinčić, Dragan, Radak, Sandra, Đurić, Tamara, Stanković, Aleksandra, "The sex-specific association of Met62Ile gene polymorphism in P-selectin glycoprotein ligand (PSGL-1) with carotid plaque presence: preliminary study" in Molecular Biology Reports, 39, no. 6 (2012):6479-6485,
https://doi.org/10.1007/s11033-012-1475-5 . .
3
3
3

Association of MMP-3 5A/6A gene polymorphism with susceptibility to carotid atherosclerosis

Đurić, Tamara; Živković, Maja; Radak, Đorđe J.; Jekić, Đole; Radak, Sandra; Stojković, Ljiljana S.; Raičević, Ranko; Stanković, Aleksandra; Alavantić, Dragan

(2008)

TY  - JOUR
AU  - Đurić, Tamara
AU  - Živković, Maja
AU  - Radak, Đorđe J.
AU  - Jekić, Đole
AU  - Radak, Sandra
AU  - Stojković, Ljiljana S.
AU  - Raičević, Ranko
AU  - Stanković, Aleksandra
AU  - Alavantić, Dragan
PY  - 2008
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3571
AB  - Objectives: Stromelysin-1 (MMP-3) as a key member of metalloproteinase family could have an important role in atherogenesis. The 5A/6A polymorphism in the promoter of MMP-3 gene affects the level of MMP-3 gene expression. We assessed whether the MMP-3 promoter low-and high-activity genotypes are related to susceptibility for carotid atherosclerosis (CA) in Serbian population. Design and methods: The study group of case-control design consisted of 515 participants. The 265 patients with ultrasonographic evidence of carotid plaque presence were recruited for the study. The 5A/6A polymorphism was typed by RFLP-PCR. Results: There was significantly higher prevalence of genotypes containing 6A allele in the patients with CA compared to controls (p LT 0.05). The model of inheritance with the dominant effect of 6A allele gave elevated and significant OR for carotid atherosclerosis (adjusted OR 2.35, CI = 1.0-5.5, p=0.048). Conclusions: Subjects carrying genotypes with 6A allele had significantly higher susceptibility to carotid atherosclerosis. (C) 2008 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
T2  - Clinical Biochemistry
T1  - Association of MMP-3 5A/6A gene polymorphism with susceptibility to carotid atherosclerosis
VL  - 41
IS  - 16-17
SP  - 1326
EP  - 1329
DO  - 10.1016/j.clinbiochem.2008.08.081
ER  - 
@article{
author = "Đurić, Tamara and Živković, Maja and Radak, Đorđe J. and Jekić, Đole and Radak, Sandra and Stojković, Ljiljana S. and Raičević, Ranko and Stanković, Aleksandra and Alavantić, Dragan",
year = "2008",
abstract = "Objectives: Stromelysin-1 (MMP-3) as a key member of metalloproteinase family could have an important role in atherogenesis. The 5A/6A polymorphism in the promoter of MMP-3 gene affects the level of MMP-3 gene expression. We assessed whether the MMP-3 promoter low-and high-activity genotypes are related to susceptibility for carotid atherosclerosis (CA) in Serbian population. Design and methods: The study group of case-control design consisted of 515 participants. The 265 patients with ultrasonographic evidence of carotid plaque presence were recruited for the study. The 5A/6A polymorphism was typed by RFLP-PCR. Results: There was significantly higher prevalence of genotypes containing 6A allele in the patients with CA compared to controls (p LT 0.05). The model of inheritance with the dominant effect of 6A allele gave elevated and significant OR for carotid atherosclerosis (adjusted OR 2.35, CI = 1.0-5.5, p=0.048). Conclusions: Subjects carrying genotypes with 6A allele had significantly higher susceptibility to carotid atherosclerosis. (C) 2008 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.",
journal = "Clinical Biochemistry",
title = "Association of MMP-3 5A/6A gene polymorphism with susceptibility to carotid atherosclerosis",
volume = "41",
number = "16-17",
pages = "1326-1329",
doi = "10.1016/j.clinbiochem.2008.08.081"
}
Đurić, T., Živković, M., Radak, Đ. J., Jekić, Đ., Radak, S., Stojković, L. S., Raičević, R., Stanković, A.,& Alavantić, D.. (2008). Association of MMP-3 5A/6A gene polymorphism with susceptibility to carotid atherosclerosis. in Clinical Biochemistry, 41(16-17), 1326-1329.
https://doi.org/10.1016/j.clinbiochem.2008.08.081
Đurić T, Živković M, Radak ĐJ, Jekić Đ, Radak S, Stojković LS, Raičević R, Stanković A, Alavantić D. Association of MMP-3 5A/6A gene polymorphism with susceptibility to carotid atherosclerosis. in Clinical Biochemistry. 2008;41(16-17):1326-1329.
doi:10.1016/j.clinbiochem.2008.08.081 .
Đurić, Tamara, Živković, Maja, Radak, Đorđe J., Jekić, Đole, Radak, Sandra, Stojković, Ljiljana S., Raičević, Ranko, Stanković, Aleksandra, Alavantić, Dragan, "Association of MMP-3 5A/6A gene polymorphism with susceptibility to carotid atherosclerosis" in Clinical Biochemistry, 41, no. 16-17 (2008):1326-1329,
https://doi.org/10.1016/j.clinbiochem.2008.08.081 . .
24
24
27

Cx3cr1 T280m Gene Polymorphism and Plaque Stability in Patients with Carotid Atherosclerosis

Stančić, O.; Živković, Maja; Stanković, Aleksandra; Đurić, Tamara; Radak, Đorđe J.; Radak, Sandra; Alavantić, Dragan

(2008)

TY  - CONF
AU  - Stančić, O.
AU  - Živković, Maja
AU  - Stanković, Aleksandra
AU  - Đurić, Tamara
AU  - Radak, Đorđe J.
AU  - Radak, Sandra
AU  - Alavantić, Dragan
PY  - 2008
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2724
C3  - Atherosclerosis Supplements
T1  - Cx3cr1 T280m Gene Polymorphism and Plaque Stability in Patients with Carotid Atherosclerosis
VL  - 9
IS  - 1
SP  - 62
EP  - 62
DO  - 10.1016/S1567-5688(08)70247-2
ER  - 
@conference{
author = "Stančić, O. and Živković, Maja and Stanković, Aleksandra and Đurić, Tamara and Radak, Đorđe J. and Radak, Sandra and Alavantić, Dragan",
year = "2008",
journal = "Atherosclerosis Supplements",
title = "Cx3cr1 T280m Gene Polymorphism and Plaque Stability in Patients with Carotid Atherosclerosis",
volume = "9",
number = "1",
pages = "62-62",
doi = "10.1016/S1567-5688(08)70247-2"
}
Stančić, O., Živković, M., Stanković, A., Đurić, T., Radak, Đ. J., Radak, S.,& Alavantić, D.. (2008). Cx3cr1 T280m Gene Polymorphism and Plaque Stability in Patients with Carotid Atherosclerosis. in Atherosclerosis Supplements, 9(1), 62-62.
https://doi.org/10.1016/S1567-5688(08)70247-2
Stančić O, Živković M, Stanković A, Đurić T, Radak ĐJ, Radak S, Alavantić D. Cx3cr1 T280m Gene Polymorphism and Plaque Stability in Patients with Carotid Atherosclerosis. in Atherosclerosis Supplements. 2008;9(1):62-62.
doi:10.1016/S1567-5688(08)70247-2 .
Stančić, O., Živković, Maja, Stanković, Aleksandra, Đurić, Tamara, Radak, Đorđe J., Radak, Sandra, Alavantić, Dragan, "Cx3cr1 T280m Gene Polymorphism and Plaque Stability in Patients with Carotid Atherosclerosis" in Atherosclerosis Supplements, 9, no. 1 (2008):62-62,
https://doi.org/10.1016/S1567-5688(08)70247-2 . .

Mmp-8 Gene Expression in Human Carotid Plaques

Đurić, Tamara; Živković, Maja; Stanković, Aleksandra; Radak, Đorđe J.; Radak, Sandra; Alavantić, Dragan

(2008)

TY  - CONF
AU  - Đurić, Tamara
AU  - Živković, Maja
AU  - Stanković, Aleksandra
AU  - Radak, Đorđe J.
AU  - Radak, Sandra
AU  - Alavantić, Dragan
PY  - 2008
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2725
C3  - Atherosclerosis Supplements
T1  - Mmp-8 Gene Expression in Human Carotid Plaques
VL  - 9
IS  - 1
SP  - 236
EP  - 236
DO  - 10.1016/S1567-5688(08)70943-7
ER  - 
@conference{
author = "Đurić, Tamara and Živković, Maja and Stanković, Aleksandra and Radak, Đorđe J. and Radak, Sandra and Alavantić, Dragan",
year = "2008",
journal = "Atherosclerosis Supplements",
title = "Mmp-8 Gene Expression in Human Carotid Plaques",
volume = "9",
number = "1",
pages = "236-236",
doi = "10.1016/S1567-5688(08)70943-7"
}
Đurić, T., Živković, M., Stanković, A., Radak, Đ. J., Radak, S.,& Alavantić, D.. (2008). Mmp-8 Gene Expression in Human Carotid Plaques. in Atherosclerosis Supplements, 9(1), 236-236.
https://doi.org/10.1016/S1567-5688(08)70943-7
Đurić T, Živković M, Stanković A, Radak ĐJ, Radak S, Alavantić D. Mmp-8 Gene Expression in Human Carotid Plaques. in Atherosclerosis Supplements. 2008;9(1):236-236.
doi:10.1016/S1567-5688(08)70943-7 .
Đurić, Tamara, Živković, Maja, Stanković, Aleksandra, Radak, Đorđe J., Radak, Sandra, Alavantić, Dragan, "Mmp-8 Gene Expression in Human Carotid Plaques" in Atherosclerosis Supplements, 9, no. 1 (2008):236-236,
https://doi.org/10.1016/S1567-5688(08)70943-7 . .

Identification of monocyte chemoattractant protein-1 gene expression in human carotid plaques

Živković, Maja; Radak, Đorđe J.; Stanković, Aleksandra; Đurić, Tamara; Rakovic, A.; Radak, Sandra; Alavantić, Dragan

(2007)

TY  - CONF
AU  - Živković, Maja
AU  - Radak, Đorđe J.
AU  - Stanković, Aleksandra
AU  - Đurić, Tamara
AU  - Rakovic, A.
AU  - Radak, Sandra
AU  - Alavantić, Dragan
PY  - 2007
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/6670
C3  - Atherosclerosis Supplements
T1  - Identification of monocyte chemoattractant protein-1 gene expression in human carotid plaques
VL  - 8
IS  - 1
SP  - 75
EP  - 75
DO  - 10.1016/S1567-5688(07)71247-3
ER  - 
@conference{
author = "Živković, Maja and Radak, Đorđe J. and Stanković, Aleksandra and Đurić, Tamara and Rakovic, A. and Radak, Sandra and Alavantić, Dragan",
year = "2007",
journal = "Atherosclerosis Supplements",
title = "Identification of monocyte chemoattractant protein-1 gene expression in human carotid plaques",
volume = "8",
number = "1",
pages = "75-75",
doi = "10.1016/S1567-5688(07)71247-3"
}
Živković, M., Radak, Đ. J., Stanković, A., Đurić, T., Rakovic, A., Radak, S.,& Alavantić, D.. (2007). Identification of monocyte chemoattractant protein-1 gene expression in human carotid plaques. in Atherosclerosis Supplements, 8(1), 75-75.
https://doi.org/10.1016/S1567-5688(07)71247-3
Živković M, Radak ĐJ, Stanković A, Đurić T, Rakovic A, Radak S, Alavantić D. Identification of monocyte chemoattractant protein-1 gene expression in human carotid plaques. in Atherosclerosis Supplements. 2007;8(1):75-75.
doi:10.1016/S1567-5688(07)71247-3 .
Živković, Maja, Radak, Đorđe J., Stanković, Aleksandra, Đurić, Tamara, Rakovic, A., Radak, Sandra, Alavantić, Dragan, "Identification of monocyte chemoattractant protein-1 gene expression in human carotid plaques" in Atherosclerosis Supplements, 8, no. 1 (2007):75-75,
https://doi.org/10.1016/S1567-5688(07)71247-3 . .