Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Cokan Vujkovac A"'
Autor:
Popović D, Nikolajević Starčević J, Šantl Letonja M, Makuc J, Cokan Vujkovac A, Reschner H, Bregar D, Petrovič D
Publikováno v:
Balkan Journal of Medical Genetics, Vol 19, Iss 1, Pp 63-70 (2016)
The platelet endothelial cell adhesion molecule 1 (PECAM-1) plays an important role in many inflammatory processes, including the development of atherosclerosis. Polymorphism rs668 of the PECAM-1 gene (373C/G) is functional, and it was reported to be
Externí odkaz:
https://doaj.org/article/fad285bde65e467388bc9cd48ba73f1b
Autor:
Merlo S, Novák J, Tkáčová N, Nikolajević Starčević J, Šantl Letonja M, Makuc J, Cokan Vujkovac A, Letonja J, Bregar D, Zorc M, Rojko M, Mankoč S, Kruzliak P, Petrovič D
Publikováno v:
Balkan Journal of Medical Genetics, Vol 18, Iss 2, Pp 37-42 (2015)
The current study was designed to reveal possible associations between the angiotensin-converting-enzyme (ACE) gene polymorphisms (rs4646994 and rs4341) with markers of carotid atherosclerosis in patients with type 2 diabetes mellitus (T2DM) in a 4-y
Externí odkaz:
https://doaj.org/article/e6dd006cc95844bcbea07a2af7e6d518
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
IntroductionEarly initiation is essential for successful treatment of Fabry disease, but sensitive and noninvasive biomarkers of Fabry nephropathy are lacking. Urinary extracellular vesicles (uEVs) represent a promising source of biomarkers of kidney
Externí odkaz:
https://doaj.org/article/ebf1a77f62fd4f9fab208476575434a5
Autor:
Tanja Planinšek Ručigaj, Matija Kozak, Ana Slana, Nikola Bešič, Andreja Cokan Vujkovac, Marko Grmek, Albin Stritar, Nada Kecelj Leskovec
Publikováno v:
Zdravniški Vestnik, Vol 87, Iss 7-8 (2018)
V prispevku so predstavljena priporočila za obravnavo bolnikov z limfedemom. Prikazana je klinična slika, diagnosticiranje in različni načini obravnave.
Externí odkaz:
https://doaj.org/article/b110bbb6b99443f780040b3f91457e8d
Autor:
Martin Tretjak, Sandra Radoš Krnel, Tajda Keber, Irena Srebotnik Kirbiš, Andreja Cokan Vujkovac, Bojan Vujkovac
Publikováno v:
Clinical Kidney Journal. 15:269-277
Background Fabry disease (FD) is a rare X-linked disorder of sphingolipid metabolism that results in chronic proteinuric nephropathy. Podocytes are one of the most affected renal cells and play an important role in the development and progression of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::957639259e568850c2893f34bffe4770
https://doi.org/10.1093/ckj/sfab172
https://doi.org/10.1093/ckj/sfab172
Autor:
Mehdi Namdar, Albert Hagège, Eloisa Arbustini, Päivi Pietilä-Effati, Aleš Linhart, Roberto Barriales-Villa, Peter Nordbeck, Johanna Kuusisto, Iacopo Olivotto, Antonia Camporeale, Andreja Cokan Vujkovac, Perry M. Elliott, Maurizio Pieroni, James C. Moon
Publikováno v:
Journal of the American College of Cardiology. 77:922-936
Fabry disease (FD) is a rare X-linked inherited lysosomal storage disorder caused by deficient α-galactosidase A activity that leads to an accumulation of globotriasylceramide (Gb3) in affected tissues, including the heart. Cardiovascular involvemen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::614addc2216fa0560a14f9eea42c7611
https://doi.org/10.1016/j.jacc.2020.12.024
https://doi.org/10.1016/j.jacc.2020.12.024
Autor:
Sebastjan Merlo, Jovana Nikolajević Starčević, Sara Mankoč, Marija Šantl Letonja, Andreja Cokan Vujkovac, Marjeta Zorc, Daniel Petrovič
Publikováno v:
Journal of Diabetes Research, Vol 2016 (2016)
Background. The current study was designed to reveal possible associations between the polymorphisms of the vascular endothelial growth factor (VEGF) gene (rs2010963) and its receptor, kinase insert domain-containing receptor (KDR) gene polymorphism
Externí odkaz:
https://doaj.org/article/49a89f00591e4e04b61d7355887f1a95
Autor:
Aleš Pleskovič, Marija Šantl Letonja, Andreja Cokan Vujkovac, Jovana Nikolajević Starćević, Danijel Petrovič
Publikováno v:
PPAR Research, Vol 2016 (2016)
Background. The present study was designed to clarify whether common single nucleotide polymorphisms (SNPs) of the Peroxisome Proliferator-Activated Receptor-γ (PPAR-γ) gene (rs1801282) and the Peroxisome Proliferator-Activated Receptor-γ Coactiva
Externí odkaz:
https://doaj.org/article/a52a8fd7ccee4f108e4750285d9c509d
Publikováno v:
Angiology. 72:426-433
Fabry disease is a rare X-linked lysosomal disorder. Alpha-galactosidase A deficiency caused by mutation leads to accumulation of glycosphingolipids predominantly in endothelial cells, leading to impairment of vascular wall morphology and function. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f35684a4f9d88098f4c59dc9d5ffbbc2
https://doi.org/10.1177/0003319720981521
https://doi.org/10.1177/0003319720981521
Autor:
Jovana Nikolajević-Starčević, Dražen Popović, Marija Šantl Letonja, Jana Makuc, Maja Šeruga, Andreja Cokan Vujkovac, Zala Jenko Pražnikar, Janez Stare, Daniel Petrovic
Publikováno v:
Zdravniški Vestnik, Vol 83, Iss 0 (2014)
Introduction Increased serum level of low density lipoprotein (LDL) cholesterol is a well established risk factor for atherosclerosis development and progression. Genetic variation in the LDL receptor gene could modulate serum LDL level and response
Externí odkaz:
https://doaj.org/article/0d66a6f4abb74ba0bb14da8f97c747b4