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Browsing by Author "Maksimovic, Z. (26537806600)"

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    Effects of human erythropoietin (ESF) on erythropoiesis in fasted guinea-pigs
    (1981)
    Mujovic, V.M. (6603462234)
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    Starcevic, V. (7005374307)
    ;
    Maksimovic, Z. (26537806600)
    [No abstract available]
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    Endovascular treatment of bilateral internal carotid artery aneurysm
    (2012)
    Končar, I. (19337386500)
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    Colic, M. (7005003692)
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    Ilic, N. (7006245465)
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    Cvetkovic, S. (7006158672)
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    Maksimovic, Z. (26537806600)
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    Davidovic, L. (7006821504)
    Background: Aneurysms of the extra cranial internal carotid artery (ICA) are rare and caused by infection, arteriosclerosis, fibro muscular dysplasia, neurofibromatosis, Behcet disease, Ehlers-Danlos syndrome, radiotherapy, iatrogenic injury or trauma. Increasing number of high-risk patients and more accurate diagnosing of unapproachable lesions make the consideration of endovascular treatment more acceptable. Methods: We are reporting a case of a 36-year-old male with bilateral aneurysms of ICA and a history of several transitory ischemic attacks. Bilateral successive implantation of a 19mm long covered stent (Jostent) was performed, with a delay of one month between the two procedures. After exclusion of the right ICA with covered stent, patient developed transitory ischemic attack and control multi detector computed tomography revealed occlusion of the left ICA. Results: Further recovery of the patient was uneventful and a control examination after 2 years show patent right ICA, occluded left ICA with no clinical consequences. Conclusions: Patients with recurrent symptoms associated with extra cranial aneurysm need prompt treatment. Surgical resection with various reconstruction techniques is established method. Endovascular exclusion by covered stent in surgically unapproachable aneurysms is feasible; however, there is still need for more technical improvement and experience before it becomes preferable treatment option. © 2012 Springer-Verlag.
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    Expression of matrix metalloproteinases and endogenous inhibitors in abdominal aortic aneurysm and aortoiliac occlusive disease (syndrome leriche)
    (2017)
    Vasic, N. (57201797483)
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    Glumac, S. (33467624700)
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    Pejic, S. (6602841944)
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    Amidzic, L.J. (57224488902)
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    Tadic Latinovic, L.J. (57201801229)
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    Dozic, B. (6507142704)
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    Hinic, S. (55208518100)
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    Maksimovic, Z. (26537806600)
    Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) play a complex role in the pathogenesis of atherosclerosis. We compared (1) the histopathological findings in patients with abdominal aortic aneurysms (AAA) and aortoiliac occlusive disease (AOD); (2) the expression of MMP-2/MMP-9 and TIMP-1/TIMP-2 in aortic layers, inflammatory cells and smooth muscle cells (SMCs), aiming to identify the common underlying pathogenic mechanisms of the disease development. Samples were obtained from 30 patients with AAA and 30 with AOD. Aortic histology and immunohistochemistry were performed to evaluate inflammatory changes and MMP and TIMP expression. Thrombosis and ulceration were more frequent in AOD than in AAA. The MMP-9 expression was elevated in all aortic layers of AAA patients and in media/adventitia of AOD patients, mainly followed by lower expression of its inhibitor TIMP-1. Higher MMP-9 expression was also found in SMCs and macrophages of both AAA and AOD specimens, while higher TIMP-1/TIMP-2 were predominantly observed in the lymphocytes and macrophages of the aneurysm. These results showed that both conditions exhibited increased MMP-9 expression; however, the MMP expression pattern differed to some degree between the aneurysms and occlusive disease. The variations in molecular mechanisms underlying dilatative/stenosing disease warrant further investigation. © 2017 Charles University. All rights reserved.
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    Risk factors in unsuccessfully treated chronic peripheric arterial insufficiency
    (1984)
    Dukic, V. (7004164526)
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    Maksimovic, Z. (26537806600)
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    Radak, D. (7004442548)
    [No abstract available]
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    Second look at congenital vascular malformations: Current classification, diagnostic and treatment principles
    (2013)
    Maksimovic, Z. (26537806600)
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    Maksimovic, M. (13613612200)
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    Koncar, I. (19337386500)
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    Ilic, N. (7006245465)
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    Dragas, M. (25027673300)
    Congenital vascular malformations (CVMs) are not rare disorders, with the overall incidence of 1.5%. Due to their complex embryology and various clinical presentations, there was a long lasting confusion among vascular specialists regarding the etiology, classification, basic principles of evaluation and treatment of these anomalies. The introduction of the Hamburg classification and its adoption by experts around the world made further studies of CVMs and comparison of results among different specialists possible. Precise diagnosis of the type and extent of the malformation is paramount for the choice of adequate treatment. In most instances this can be achieved with a detailed history, careful physical examination and a combination of appropriate non-invasive studies. Invasive tests should be reserved for confirmation of diagnosis and serve as a road map for treatment planning. Modern treatment of CVMs is based on a multidisciplinary team approach involving specialists in vascular surgery, interventional radiology, pediatrics, nuclear medicine, orthopedic surgery, plastic and reconstructive surgery and physical therapy. Surgical and endovascular techniques are used in conjunction to minimize morbidity and improve treatment outcomes.

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