Zobrazeno 1 - 10
of 114
pro vyhledávání: '"Vujić Dragana"'
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 152, Iss 9-10, Pp 520-523 (2024)
Introduction. The Hickman catheter is a tunneled, open-type catheter often implanted in children for long-term intravenous treatment. Their application can cause numerous complications. Catheter breakage and dislocation of fragments to the intravascu
Externí odkaz:
https://doaj.org/article/df63b22cce4740a188f1e16680c4c606
Autor:
Todorović-Balint Milena, Bila Jelena, Balint Bela, Jeličić Jelena, Đunić Irena, Antić Darko, Kraguljac-Kurtović Nada, Vujić Dragana, Mihaljević Biljana
Publikováno v:
Vojnosanitetski Pregled, Vol 77, Iss 8, Pp 844-851 (2020)
Background/Aim. Autologous stem cell transplants (ASCTs) improve the rate of overall survival (OS) in patients with hematological malignancies such as multiple myeloma (MM) after induction chemotherapy, aggressive non-Hodgkin's lymphomas (NHL), and r
Externí odkaz:
https://doaj.org/article/57f56c6671cf4c9dbb3ce67f32f68606
Autor:
Šerbić-Nonković Olivera, Kuzmanović Miloš, Životić Maja, Žunić Svetlana, Jovičić-Gojkov Dragana, Vujić Dragana
Publikováno v:
Vojnosanitetski Pregled, Vol 75, Iss 4, Pp 390-397 (2018)
Background/Aim. Transfusion reaction is an adverse event which manifests during or after administration of blood components to the patient. We aimed to show less known aspects of most common transfusion reactions (allergic and febrile non-hemolytic t
Externí odkaz:
https://doaj.org/article/084d38fb252e4129967cbf9051f1e0d2
Autor:
Milenković Tatjana, Vujić Dragana, Vuković Rade, Zečević Željko, Soldatović Ivan, Mitrović Katarina, Todorović Slađana, Zdravković Dragan
Publikováno v:
Vojnosanitetski Pregled, Vol 71, Iss 12, Pp 1123-1127 (2014)
Background/Aim. Although total body irradiation (TBI) was considered to be the primary cause of thyroid dysfunction following hematopoietic stem cells transplantation (HSCT), a significant prevalence of subclinical hypothyroidism after HSCT with c
Externí odkaz:
https://doaj.org/article/25afe48d62c444fda1befb857880a9d8
Publikováno v:
Vojnosanitetski Pregled, Vol 71, Iss 4, Pp 368-372 (2014)
Background/Aim. Fanconi anemia (FA) is a rare hereditary disease in a heterogeneous group of syndromes, so-called chromosome breakage disorders. Specific hypersensitivity of its cells to chemical agents, such as diepoxybutane (DEB), was used as a
Externí odkaz:
https://doaj.org/article/8f4cf6c2ccf84dc0a097652e05271ce6
Autor:
Vujić Dragana S., Petrović Sandra Ž., Leskovac Andreja R., Joksić Ivana D., Filipović Jelena G., Valenta-Šobot Ana P.
Publikováno v:
Nuclear Technology and Radiation Protection, Vol 28, Iss 2, Pp 221-224 (2013)
In this paper we present the data of lymphocyte radiosensitivity testing used for characterization of radiosensitive cellular phenotype and diagnostics of ataxia-telangiectasia disease. We point out the advantage of lymphocyte micronucleus test (CBMN
Externí odkaz:
https://doaj.org/article/bf56e78ef93d4b2884e82e88078b6670
Autor:
Petrović Sandra, Vujić Dragana, Guć-Šćekić Marija, Leskovac Andreja, Jevtić Dragana, Joksić Gordana
Publikováno v:
Archives of Biological Sciences, Vol 61, Iss 2, Pp 195-204 (2009)
Fanconi anemia (FA) is a genetic disease characterized by progressive pancytopenia and cancer susceptibility. The clinical and cellular phenotypes of Fanconi anemia are associated with a set of redox abnormalities, indicating that FA is an oxidativ
Externí odkaz:
https://doaj.org/article/ae2da3a60e554633b7fa1957c857ce6f
Autor:
Krstić Aleksandra D., Stojković O., Guć-Šćekić Marija, Vujić Dragana, Jevtić Dragana, Varljen Tanja
Publikováno v:
Archives of Biological Sciences, Vol 59, Iss 1, Pp 23-27 (2007)
Hematopoietic stem cell transplantation (HSCT) is a very successful method of treatment for children with different aquired or inborn diseases. The main goal of post-transplantation chimerism monitoring in HSCT is to predict negative events (such as
Externí odkaz:
https://doaj.org/article/2a0d702f0cb74ba981aa11162961b49d
Publikováno v:
Archives of Biological Sciences, Vol 58, Iss 4, Pp 215-219 (2006)
Fanconi anemia (FA) is an inherited disorder with aplastic anemia, cancer susceptibility, and hypersensitivity to alkylating agents such as diepoxybutane (DEB). The DEB test is used to screen for FA among patients with bone marrow failure syndromes (
Externí odkaz:
https://doaj.org/article/82fa640b0b2e41b98b2fc0d5a9c9a1b9
Autor:
Slavković Bojana, Guć-Šćekić Marija, Bunjevački Gordana, Đuričić S., Krstić Aleksandra, Mićić D., Vujić Dragana, Kuzmanović M., Rašović-Gvozdenović Nada
Publikováno v:
Archives of Biological Sciences, Vol 57, Iss 1, Pp 11-17 (2005)
The aim of this study was to investigate distribution of immunophenotypic and cytogenetic features of childhood acute leukemia (AL) in the cohort of 239 newly diagnosed patients registered at the leading pediatric oncohematology center in the country
Externí odkaz:
https://doaj.org/article/4a8d809007d74ceea39a436045ef9895