Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Zorica Raskovic"'
Autor:
Andjelka Stojkovic, Irena Ilic, Andrijana Kostic, Katerina Dajic, Zorica Raskovic, Jelena Nestorovic, Milena Ilic
Publikováno v:
Diagnostics, Vol 13, Iss 17, p 2826 (2023)
When hypostatic pneumonia is present at the same time as COVID-19 pneumonia, the clinical course is almost always prolonged (prolonged-COVID-19) due to persistent inflammation, long-term anti-inflammatory syndrome, followed by immune exhaustion, i.e.
Externí odkaz:
https://doaj.org/article/3413fe2e640e431aa773898ed72b7a59
The Different Clinical Courses of Legionnaires’ Disease in Newborns from the Same Maternity Hospital
Autor:
Andrijana Kostic, Katarina Cukovic, Lidija Stankovic, Zorica Raskovic, Jelena Nestorovic, Dragana Savic, Aleksandra Simovic, Tijana Prodanovic, Suzana Zivojinovic, Sladjana Andrejevic, Ismihana Erovic, Zorana Djordjevic, Snezana Rsovac, Predrag Sazdanovic, Andjelka Stojkovic
Publikováno v:
Medicina, Vol 58, Iss 9, p 1150 (2022)
In children, the incidence of Legionnaires’ disease (LD) is unknown, hospital-acquired LD is associated with clinical risk factors and environmental risk, and children with cell-mediated immune deficiency are at high risk of infection. Both newborn
Externí odkaz:
https://doaj.org/article/afbd635c4c194ea9854e3569734cfcd2
Autor:
Zoran Igrutinovic, Biljana Vuletic, Gordana Kostic, Milan Paunovic, Rasa Medovic, Nevena Folic, Dragana Savic, Zorica Raskovic, Slavica Markovic
Publikováno v:
Serbian Journal of Experimental and Clinical Research, Vol 22, Iss 3, Pp 271-275 (2021)
Wandering spleen is a very rare clinical condition characterized by spleen absence in the normal anatomical location in the upper left quadrant of the abdomen and its presence at another location in the abdomen or pelvis. The ectopic spleen is extrem
Autor:
Jelena Nestorovic-Tanaskovic, Zoran Igrutinovic, Biljana Vuletic, Маrija Radovanovic, Jovana Dabovic, Dragana Savic, Raša Medovic, Zorica Raskovic, Sanja Knezevic-Rangelov, Slobodan Obradovic
Publikováno v:
Serbian Journal of Experimental and Clinical Research.
Apert syndrome (Acrocephalosyndactylia type 1) belongs to the group of extremely rare congenital dysmorphic syndromes. It is characterized by craniostenosis with very early fusion of the skull and / or cranial base sutures, facial hypoplasia, symmetr
Autor:
Vojislav Cupurdija, Zoran Igrutinovic, Slavica Markovic, Rasa Medovic, Zorica Raskovic, Gordana Kostic, Marina Petrovic
Publikováno v:
Vojnosanitetski Pregled, Vol 75, Iss 5, Pp 516-520 (2018)
Introduction. After the contact with a patient suffering from tuberculosis (TB), previously healthy children have 1%?16% possibility to develop the disease. TB diagnosis in children is not easy to confirm so 15%?25% of cases remain undiagnosed. Case
Autor:
Biljana Vuletic, Slavica Markovic, Vladimir Radlovic, Zorica Raskovic, Zoran Igrutinovic, Elizabeta Ristanovic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 145, Iss 1-2, Pp 85-88 (2017)
Clostridium difficile (CD) is the most common cause of nosocomial diarrhea in adults with high rates of morbidity and mortality. The epidemiology of CD infection (CDI) has changed in the last few decades associated with increasing severity of the inf
Autor:
Biljana Vuletic, Slavica Markovic, Zoran Igrutinovic, Vladimir Radlovic, Zorica Raskovic, Jelena Tanaskovic-Nestorovic, Aleksandra Simovic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 144, Iss 1-2, Pp 90-93 (2016)
Introduction. Hypocalcemic seizures are uncommon in the post-neonatal period. We report an infant with hypocalcemic seizures caused by severe deficiency of vitamin D. Case Outline. A five-month-old male infant was admitted to hospital in March 2013 w
Autor:
Rasa Medovic, Zoran Igrutinovic, Jelena Nestorovic–Tanaskovic, Aleksandra Simovic, Biljana Vuletic, Zorica Raskovic
Publikováno v:
Serbian Journal of Experimental and Clinical Research, Vol 16, Iss 1, Pp 55-63 (2015)
Secondary haemophagocytic lymphohistiocytosis (SHFLH) is a rare, potentially fatal disorder, most commonly caused by the Epstein–Barr virus. It is characterized by neoplastic proliferation of cells that belong to the monocyte–macrophage system an
Autor:
Zoran Igrutinovic, Jasmina Knežević, Milan Djukic, Jasmina Knezevic, Zorica Raskovic, Aleksandra M. Simovic, Jelena M. Nestorovic-Tanaskovic
Publikováno v:
Medicinski casopis. 48:136-139
Introduction. Dysplastic or myxomatous mitral valve is characterized by myxomatous degeneration of collagen and elastin which causes excess growth of mitral valves. In due course, some pathological characteristics may develop, such as mitral valves p
Publikováno v:
Serbian Journal of Experimental and Clinical Research. 14:175-179
Congenital hepatic fi brosis (CHF) is a rare developmental disorder of the portobiliary system and most commonly associated with polycystic kidney disease. The pattern of inheritance of this disorder is autosomal recessive. The exact prevalence of CH