Zobrazeno 1 - 10
of 246
pro vyhledávání: '"Marković Olivera"'
Publikováno v:
Archives of Biological Sciences, Vol 75, Iss 2, Pp 125-131 (2023)
Biological aspects (length frequency distribution, length-weight ratio, sex ratio, allometric growth, Fulton’s condition factor) of Upogebia pusilla were studied in Tivat Saline (Tivatska solila), Boka Kotorska Bay in 2019. A total of 1,415 individ
Externí odkaz:
https://doaj.org/article/5108b702f27f4c0e8e3e8ec4bb251e44
Publikováno v:
Vojnosanitetski Pregled, Vol 79, Iss 10, Pp 1044-1047 (2022)
Introduction. Although secondary malignancies usually occur at different times after hairy cell leukemia (HCL) treatment, the occurrence of HCL and other malignancies at the same time is very rare. Synchronous HCL and diffuse large B-cell lymphoma (D
Externí odkaz:
https://doaj.org/article/8f9efe09a7b64b5da610e6edec6fb38a
Autor:
Marković Olivera, Martinović Tamara, Ćirić Darko, Trpinac Dušan, Čemerikić-Martinović Vesna, Bumbaširević Vladimir, Bila Jelena, Marisavljević Dragomir, Kravić-Stevović Tamara
Publikováno v:
Vojnosanitetski Pregled, Vol 76, Iss 7, Pp 740-744 (2019)
Introduction. Congenital asplenia is an extremely rare condition that can be separate entity due to a specific defect of spleen development or may occur in the context of a malformation syndrome. The patients with asplenia have thrombocytosis and sus
Externí odkaz:
https://doaj.org/article/a15499406aaf49349fd654d39ab4d463
Autor:
Marković Olivera, Janić Dragana, Pavlović Milorad, Tukić Ljiljana, Janković Srđa, Filipović Branka, Marisavljević Dragomir
Publikováno v:
Vojnosanitetski Pregled, Vol 74, Iss 5, Pp 494-497 (2017)
Introduction. Hemophagocytic lymphohistiocytosis (HLH) is a rare, potentially life-threatening, hyperinflammatory syndrome caused by severe hypercytokinemia due to a highly stimulated, but ineffective immune response. Case report. We reported a 19-ye
Externí odkaz:
https://doaj.org/article/e9018627b5d747e7b6fca63b338810b6
Publikováno v:
Vojnosanitetski Pregled, Vol 72, Iss 11, Pp 1039-1043 (2015)
Introduction. Good’s syndrome is a rare cause of adultonset immunodeficiency associated with thymoma. Good’s syndrome should be considered in patients older than 40 years with the history of frequent infections. An abnormal immunoglobulin prof
Externí odkaz:
https://doaj.org/article/a079085d42b94f76973cc9910b497046
Autor:
Hajder Jelena, Marisavljević Dragomir, Stanisavljević Nataša, Mihaljević Biljana, Kovčin Vladimir, Marković Olivera, Živković Radmila
Publikováno v:
Vojnosanitetski Pregled, Vol 71, Iss 11, Pp 1040-1044 (2014)
Bacground/Aim. Mucosa-associated lymphoid tissue (MALT) lymphoma accounts for 5-17% non-Hodgkin lymphomas (NHL). The molecular pathogenesis of MALT lymphomas is not well-established. The aim of this study was to evaluate immunohistochemically dete
Externí odkaz:
https://doaj.org/article/9c7e0bee2d0746379ee45a1d3e7e4dae
Autor:
Marković Olivera, Marisavljević Dragomir, Jelić Svetlana, Mihaljević Biljana, Martinović Tamara, Čemerikić Vesna
Publikováno v:
Vojnosanitetski Pregled, Vol 71, Iss 7, Pp 689-692 (2014)
Introduction. Primary adrenal non-Hodgkin’s lymphoma (NHL) is a rare neoplasm with poor prognosis. On the other side, double-hit lymphomas with BCL2 and MYC translocation are characterized by advanced disease stage, extranodal and central nervou
Externí odkaz:
https://doaj.org/article/243014d14f5b4d8fac69b5a0604438bc
Publikováno v:
Vojnosanitetski Pregled, Vol 72, Iss 4, Pp 383-385 (2015)
Introduction. Primary myelofibrosis (PMF) is a clonal myeloproliferative neoplasm that occurs most commonly in the decade six of life and it is very rare in the young persons. Case report. We reported a 28-year-old female patient with primary myel
Externí odkaz:
https://doaj.org/article/367e2ea0730f43dcba99bb7585d61a7c
Publikováno v:
Vojnosanitetski Pregled, Vol 72, Iss 5, Pp 466-468 (2015)
Introduction. There are only a few available data about hairy cell leukemia (HCL) in very old patients. We presented three very different cases of HCL in very old patients diagnosed in a single center and discussed some epidemiological and therape
Externí odkaz:
https://doaj.org/article/abe6d03760804e70b698e149adbf5b02
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 138, Iss 3-4, Pp 240-243 (2010)
Introduction. Thrombocytopenia is a common finding in chronic liver diseases and it is caused by different pathophysiological mechanisms. Immunologic thrombocytopenic purpura (ITP) in hepatitis C infection is a distinct clinical entity. Possible reas
Externí odkaz:
https://doaj.org/article/8f54ebe8fab8441b8d954a82defadbfb