Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Stojisavljević Marko"'
Autor:
Rabrenović Violeta, Nikolić Bojan, Rabrenović Milorad, Petrović Milica, Milojević Ana, Škuletić Vesna, Živojinović Dragan, Dulović Dragan, Stojisavljević Marko, Mirosavljević Svetlana, Ristić Saša, Pantović Miloje, Petrović Marijana, Obrenčević Katarina, Pilčević Dejan, Rančić Nemanja
Publikováno v:
Vojnosanitetski Pregled, Vol 78, Iss 2, Pp 265-272 (2021)
Introduction. Kidney failure in multiple myeloma is some-times initial symptomatology and a very serious complication with an unfavorable effect on the course and prognosis of the disease. Multiple myeloma is a disease characterized by the proliferat
Externí odkaz:
https://doaj.org/article/95cbaeaf4ed34af79b2205319c0b3854
Autor:
Lončarević Olivera, Aćimović Slobodan, Vuković Jelena, Stojisavljević Marko, Marić Nebojša, Lončarević Slobodan, Petrović Marina, Milivojević Ivana, Ignjić Gordana, Milić Gordana, Mirilo Leonida, Rančić Nemanja
Publikováno v:
Vojnosanitetski Pregled, Vol 75, Iss 12, Pp 1157-1164 (2018)
Background/Aim. Lung cancer is one of the most common malignant tumors. About 80% of all lung cancers are non-small cell lung cancer (NSCLC). According to histopathological characteristics, the most common types of NSCLC are squamous cell carcinoma a
Externí odkaz:
https://doaj.org/article/bfdc17adfa8744e1ace551117378a4cf
Hereditary hemorrhagic telangiectasia with bilateral pulmonary vascular malformations: A case report
Autor:
Lončarević Olivera, Rusović Siniša, Stojisavljević Marko, Vuković Jelena, Plavec Goran, Aćimović Slobodan, Cvetković Gordana, Petrović Marina
Publikováno v:
Vojnosanitetski Pregled, Vol 73, Iss 10, Pp 956-960 (2016)
Introduction. Hereditary hemorrhagic telangiectasia (HHT) also known as Osler-Weber-Rendu syndrome is an autosomal dominant disease that occurs due to vascular dysplasia associated with the disorder in the signaling pathway of transforming growth fac
Externí odkaz:
https://doaj.org/article/0682ab589b394c99987500142bdc6717
Autor:
Novković Dobrivoje, Škuletić Vesna, Vuković Jelena, Cerović Snežana, Tomić Ilija, Karličić Vukojica, Stojisavljević Marko
Publikováno v:
Vojnosanitetski Pregled, Vol 70, Iss 5, Pp 516-521 (2013)
Introduction. Bronchial carcinoids belong to a rare type of lung tumors. If they do not expose outstanding neuroendocrine activity, they develop without clearly visible symptoms. They are often detected during a routine examination. According to thei
Externí odkaz:
https://doaj.org/article/95412713e5ed4af6a650d67b0eb74a65
Publikováno v:
Vojnosanitetski Pregled, Vol 67, Iss 10, Pp 867-870 (2010)
Background. The Mounier-Kuhn syndrome (MKS) or tracheobronchomegaly (TBM) is a rare condition of unknown frequency, up to now about 100 cases have been reported. It presents by marked dilatation of the trachea and major bronchi, recurrent respiratory
Externí odkaz:
https://doaj.org/article/ccf9d0d306564ef3bc7b614cfdf65459
Publikováno v:
Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia. Oct2010, Vol. 67 Issue 10, p867-870. 4p. 3 Black and White Photographs, 1 Chart.