Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Dragomir Marisavljevic"'
Autor:
Natasa Stanisavljevic, Ljudmila Stojanovich, Aleksandra Djokovic, Brankica Todic, Violeta Dopsaj, Jovica Saponjski, Dusan Saponjski, Olivera Markovic, Cristina Belizna, Marija Zdravkovic, Dragomir Marisavljevic
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 20, p 12309 (2022)
Objective: The potential contribution of asymmetric dimethylarginine (ADMA) and high-sensitivity C reactive protein (hsCRP) to endothelial dysfunction in APS patients has not been studied in detail, until now. The study involved 105 APS patients (59
Externí odkaz:
https://doaj.org/article/835fa87d1c94438d9cb9d21e90b67e5b
Publikováno v:
Srpski arhiv za celokupno lekarstvo. 150:602-605
Introduction. B-cell chronic lymphocytic leukemia (CLL) can be easily overlooked in pregnancy, particularly in cases with inadequate antenatal care. We report a case of pregnant woman diagnosed with CLL and evaluate this patient with cases in literat
Publikováno v:
Medical review. 75:38-43
Introduction. The myelodysplastic syndromes are a group of clonal haematopoietic stem cell disorders characterized by cytopenia, dysplasia, ineffective hematopiesis, recurrent genetic abnormalities, and increased risk of developing acute myeloid leuk
Publikováno v:
Medical review. 75:32-37
Introduction. We present the recommendations for treatment of the lower-risk myelodysplastic syndromes on behalf of the Serbian myelodysplastic syndromes group. Material and Methods. A literature review was conducted using the following bibliographic
Publikováno v:
Vojnosanitetski pregled. 79:1044-1047
Introduction: Although secondary malignancies usually occur at different times after HCL treatment, (simultaneous) occurrence of HCL and other malignancies at the same time is very rare. Synchronous hairy cell leukemia (HCL) and diffuse large B cell
Publikováno v:
Vojnosanitetski pregled. 79:204-205
nema
Autor:
Vladimir Bumbasirevic, Jelena Bila, Darko Ciric, Tamara Kravic-Stevovic, Tamara Martinovic, Olivera Markovic, Dušan Trpinac, Dragomir Marisavljevic, V. Cemerikic-Martinovic
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
Publikováno v:
Vojnosanitetski Pregled, Vol 78, Iss 6, Pp 691-692 (2021)
nema
Autor:
Ljiljana Tukic, Dragana Janic, Dragomir Marisavljevic, Olivera Markovic, Branka Filipovic, Milorad Pavlovic, Srdja Jankovic
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
Autor:
Natasa, Colovic, Dragomir, Marisavljevic, Nada, Kraguljac-Kurtovic, Andrija, Bogdanovic, Mirjana, Gotic
Publikováno v:
Archives of Iranian medicine. 22(5)
Treatment of hairy cell leukemia (HCL) with alfa-interferon and purine analogs significantly prolongs survival in these patients. However, with life prolongation, an increased risk of secondary malignancies has been reported. Acute myeloid leukemia (