Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Jelena Karadzic"'
Autor:
Marija S Trenkic Bozinovic, Gordana Stankovic Babic, Maja Petrovic, Jelena Karadzic, Tatjana Sarenac Vulovic, Milan Trenkic
Publikováno v:
Journal of Research in Medical Sciences, Vol 24, Iss 1, Pp 55-55 (2019)
Background: Chloroquine and hydroxychloroquine are drugs that are primarily used for the treatment of malaria and are also recommended for treating connective tissue disorders, autoimmune diseases, and some dermatological and inflammatory diseases. T
Externí odkaz:
https://doaj.org/article/72579095981a4194b480e3d7e9f85f27
Autor:
Jelena Karadzic, Jovana Vukadinovic, Igor M. Kovacevic, Aleksandra Radosavljević, Ivan Stefanovic
Publikováno v:
Vojnosanitetski Pregled, Vol 77, Iss 12, Pp 1245-1251 (2020)
Background/Aim. Ocular trauma is a significant cause of visual impairment worldwide. The aim of the study was to analyze clinical characteristics of patients with penetrating eye injuries with retained intraocular foreign body (IOFB) in posterior seg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09e1cc793d0c50c1c1343347d3af9116
https://doi.org/10.2298/vsp181027193k
https://doi.org/10.2298/vsp181027193k
Publikováno v:
Vojnosanitetski Pregled, Vol 76, Iss 8, Pp 843-846 (2019)
Introduction. The Alstr?m syndrome (AS) is an extremely rare autosomal recessive genetic disorder, affecting fewer than 1: 1,000,000 people globally. It is a single gene disorder due to the mutation of ALMS1 on chromosome 2 (2p13). The AS affects mul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01eee566545cda7005f2e7331585b184
https://doi.org/10.2298/vsp170314160k
https://doi.org/10.2298/vsp170314160k
A 42-year-old female with past medical history of biopsy-proven interstitial nephritis that lasted for 2 years presented with bilateral anterior uveitis that lasted 5 months. The patient was treated with systemic and local corticosteroids and local m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae8988539313780d8dfc5361ca8bffe0
https://doi.org/10.1016/b978-0-323-69541-1.00011-2
https://doi.org/10.1016/b978-0-323-69541-1.00011-2
Autor:
Tomas S. Aleman, Sruthi Arepalli, Rubens Belfort, Frederick R. Blodi, Bahram Bodaghi, Weilin Chan, Peter Yuwei Chang, Marie-Lyne Belair, Eric Fortin, Erika Massicotte, Sarah Chorfi, Christopher Conrady, Dean Eliott, C. Stephen Foster, Danielle Trief, Muhammad Hassan, Swathi Kaliki, Henry J. Kaplan, Jelena Karadzic, Madison E. Kerley, Ashleigh L. Levison, Aaron Lindeke-Myers, George Magrath, Albert M. Maguire, Caroline L. Minkus, Bobeck S. Modjtahedi, Judith Mohay, Kareem Moussa, Marion Ronit Munk, Quan Dong Nguyen, Neil Onghanseng, George N. Papaliodis, Kathryn Pepple, Aleksandra Radosavljevic, Aparna Ramasubramanian, Sivakumar R. Rathinam, Mohammad Ali Sadiq, Harpal S. Sandhu, Jessica G. Shantha, Ryan A. Shields, Lucia Sobrin, Dinu Stanescu, Kim Anne Strässle, Eric Suhler, Aristomenis Thanos, Sara Touhami, Adelaide Toutee, Eduardo Uchiyama, Russell Neil Van Gelder, Camila V. Ventura, Liana O. Ventura, Albert Vitale, Steven Yeh, Manfred Zierhut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1b668d1b441d2e91eb29161299bdce8
https://doi.org/10.1016/b978-0-323-69541-1.00086-0
https://doi.org/10.1016/b978-0-323-69541-1.00086-0
A 36-year-old woman with systemic lupus erythematosus developed multiorgan involvement, including occlusive retinal vasculopathy and cystoid macular edema. Management of her ocular complications included combined laser photocoagulation, as well as im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ee96dce4bb7f8fdcf3ad623cb2bdd18
https://doi.org/10.1016/b978-0-323-69541-1.00052-5
https://doi.org/10.1016/b978-0-323-69541-1.00052-5
Publikováno v:
Vojnosanitetski Pregled, Vol 75, Iss 10, Pp 1041-1044 (2018)
Introduction. Juvenile nasopharyngeal angiofibromas are highly vascular, locally aggressive lesions, that affect male adolescents. The surgery is the treatment of choice, although it shows a strong propensity to bleed during surgical removal. Preoper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef2624551581f892a4290d5051835c8e
http://www.doiserbia.nb.rs/img/doi/0042-8450/2018/0042-84501600388P.pdf
http://www.doiserbia.nb.rs/img/doi/0042-8450/2018/0042-84501600388P.pdf
Publikováno v:
Medicinski podmladak. 68:29-34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78663de4ea511147834705e43cde2610
https://doi.org/10.5937/mp68-13882
https://doi.org/10.5937/mp68-13882
Autor:
Bojana Radovic, Dragana Kovacevic-Pavicevic, Olgica Djurković-Djaković, Aleksandra Radosavljević, Ivan Stefanovic, Igor Kovačević, Jelena Karadzic
Publikováno v:
Vojnosanitetski pregled (2017) 74(3):212-218
Vojnosanitetski pregled
Vojnosanitetski Pregled, Vol 74, Iss 3, Pp 212-218 (2017)
Vojnosanitetski pregled
Vojnosanitetski Pregled, Vol 74, Iss 3, Pp 212-218 (2017)
Background/Aim. Rhegmatogenous retinal detachment is a potentially blinding condition of the posterior segment of the eye. Currently, the only treatment modality is surgery and surgical options include scleral buckling, pars plana vitrectomy and pneu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc7d42c58fc938a1cf676e02117dbee8
https://doi.org/10.2298/vsp141001175k
https://doi.org/10.2298/vsp141001175k
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 145, Iss 5-6, Pp 296-300 (2017)
Introduction. Retinitis pigmentosa (RP) is a group of inherited retinal dystrophies caused by mutations in various genes. The disease leads to progressive photoreceptors loss (rods predominantly) and retinal pigment epithelium alteration. RP can lead
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9538a0af194e58ca0ccb744143080494
https://doi.org/10.2298/sarh160421052k
https://doi.org/10.2298/sarh160421052k