Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Vladimir Radlovic"'
Autor:
Sinisa Ducic, Filip Milanovic, Mikan Lazovic, Bojan Bukva, Goran Djuricic, Vladimir Radlovic, Dejan Nikolic
Publikováno v:
Children, Vol 9, Iss 5, p 762 (2022)
Background: The forearm is the most common fracture site in childhood, accounting for every fourth pediatric fracture. It is well described that vitamin D is involved in the regulation of bone mineralization and skeletal homeostasis by the regulation
Externí odkaz:
https://doaj.org/article/e359309337c14a4594437c77a2371256
Autor:
Vladimir Radlovic, Zoran Golubovic, Zoran Lekovic, Sinisa Ducic, Nedeljko Radlovic, Branislav Jovanovic, Bojan Bukva, Polina Pavicevic, Dejan Nikolic, Jovana Jankovic
Publikováno v:
Srpski arhiv za celokupno lekarstvo. 151:186-189
Introduction/Objective. Gilbert syndrome (GS) is the most common hereditary hyperbilirubinemia. As well as mild unconjugated hyperbilirubinemia, it is characterized by the excess of bilirubin monoglucuronide over diglucuronide in the bile and thus in
Autor:
Phepy G. A. Dawod, Jasna Jancic, Ana Marjanovic, Marija Brankovic, Milena Jankovic, Janko Samardzic, Ayman Gamil Anwar Dawod, Ivana Novakovic, Fayda I. Abdel Motaleb, Vladimir Radlovic, Vladimir S. Kostic, Dejan Nikolic
Publikováno v:
Diagnostics, Vol 11, Iss 11, p 1969 (2021)
Mitochondrial encephalomyopathies (MEMP) are heterogeneous multisystem disorders frequently associated with mitochondrial DNA (mtDNA) mutations. Clinical presentation varies considerably in age of onset, course, and severity up to death in early chil
Externí odkaz:
https://doaj.org/article/efad65c1e5054e169c32f3dbdc13deda
Autor:
Biljana Vuletic, Aleksandar Kocovic, Marija Mladenovic, Zoran Lekovic, Vladimir Radlovic, Biljana Stojanovic, Nela Djonovic, Nedeljko Radlovic
Publikováno v:
Srpski arhiv za celokupno lekarstvo. 150:108-112
Gluten-related disorders are a heterogeneous group of clinical entities caused by intolerance to wheat, rye, and barley flour components. They occur in 3?5% of genetically predisposed persons and, based on pathogenic and clinical features, are classi
Autor:
Ivana Dasic, Jelena Radlovic, Marija Mladenovic, Bojan Bukva, Biljana Vuletic, Sinisa Ducic, Nedeljko Radlovic, Zoran Lekovic, Jelena Mandić, Vladimir Radlovic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 149, Iss 1-2, Pp 48-52 (2021)
Introduction/Objective. Nonclassical celiac disease (CD) is characterized by a very heterogeneous and non-specific clinical presentation. The aim of this study was to determine the basic symptoms and clinical signs of this CD subtype in children and
Autor:
Vladimir Radlovic, Vladimir Zugic, Rade Milic, Ivan Soldatovic, Biljana Lazovic, Sanja Sarac, Nevena Jovicic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 149, Iss 3-4, Pp 167-173 (2021)
Introduction/Objective. Cardiovascular disease is one of the most common comorbidities among subjects with chronic obstructive pulmonary disease (COPD). The aim of this study is to evaluate electrocardiogram (ECG) parameters and mortality predictors
Autor:
Biljana Vuletic, Vladimir Radlovic, Nela Djonovic, Biljana Stojanović, Stevan Jovanović, Sveta Jankovic
Publikováno v:
Vojnosanitetski Pregled, Vol 78, Iss 3, Pp 370-375 (2021)
nema
Autor:
Nedeljko Radlovic, Vladimir Radlovic, Ivana Dasic, Goran Djuricic, Nevena Jovicic, Zoran Lekovic, Marija Mladenovic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 149, Iss 3-4, Pp 221-224 (2021)
Introduction. Celiac crisis is a rare and life-threatening complication of celiac disease. Although it occurs in all ages, the most common affects children within the first two years. Outline of cases. We report three infants (two female, one male, a
Autor:
V. Bumbasirevic, Miroslav L. Djordjevic, Vladimir Radlovic, Borko Stojanovic, Bojan Bukva, Sinisa Ducic, Mikan Lazović
Publikováno v:
International Orthopaedics. 45:1065-1070
Intracondylar T-type fractures of distal humerus represent a rare condition in paediatric population with unknown incidence since the literature is limited to case reports or case series. The main purpose of this article is to provide a comprehensive
Autor:
Meho Mahmutovic, Snežana Petrović-Tepić, Zoran Lekovic, Goran Đurićić, Sinisa Ducic, Zoran Golubovic, Nedeljko Radlovic, Vladimir Radlovic, Polina Pavićević, Marija Mladenovic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 148, Iss 1-2, Pp 48-51 (2020)
Introduction/Objective. Benign transient hyperphosphatasemia (BTH) is a pathogenetic insufficiently clear clinical entity that is mostly seen in infants and young children. The objective of this paper is to present our experience regarding the age of