Zobrazeno 1 - 10
of 70
pro vyhledávání: '"BRDAR, Radivoj"'
Autor:
Dučić Siniša, Bumbaširević Marko, Radlović Vladimir, Nikić Petar, Bukumirić Zoran, Brdar Radivoj, Radojičić Zoran, Bukva Bojan, Abramović Dušan, Jaramaz-Dučić Tatjana
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 144, Iss 1-2, Pp 46-51 (2016)
Introduction. Closed reduction and percutaneous pinning are the most widely used treatment options for displaced supracondylar humerus fractures in children, but there is still no consensus concerning the most preferred technique in injuries of th
Externí odkaz:
https://doaj.org/article/ab634ea0b0dc4203b5c935197ddff581
Autor:
Dzamic Dragana, Petronic Ivana, Nikolic Dejan, Cirovic Dragana, Knezevic Tatjana, Brdar Radivoj
Publikováno v:
Scripta Medica, Vol 44, Iss 2, Pp 86-89 (2013)
Introduction. We evaluated the effectiveness of different methods of conservative treatment modalities for the treatment of idiopathic scoliosis in children. Patients and Methods. The study included 61 patients with scoliosis. The modalities of physi
Externí odkaz:
https://doaj.org/article/5460688ab7024b3a90f4272e3d0e84a7
Autor:
Leković Zoran, Radlović Nedeljko, Brdar Radivoj, Vuletić Biljana, Janić Nenad, Ristić Dragana, Stojšić Zorica, Radlović Vladimir, Simić Dušica, Nikolić Dejan
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 139, Iss 3-4, Pp 170-173 (2011)
Introduction. Idiopathic ulcerative colitis (IUC) represents a rare disease of childhood. It usually occurs at age over 10 years, and below that exceptionally rarely. Objective. The aim of the paper was to analyze the clinical signs, symptoms and the
Externí odkaz:
https://doaj.org/article/e93c4ca0580344c3824853b7ecdd70db
Autor:
Radlović Nedeljko, Ristić Dragana, Brdar Radivoj, Janić Nenad, Leković Zoran, Janić Dragana, Smoljanić Željko, Dokmanović Lidija, Jovanović Miodrag
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 139, Iss 5-6, Pp 386-389 (2011)
Introduction. Biliary calculosis is rare in children. It occurs associated with different haemolytic and non-haemolytic disorders, which are sometimes also combined. Case Outline. A 15-year-old male was hospitalized due to biliary calculosis and non-
Externí odkaz:
https://doaj.org/article/3cdf6103f04f4ddab7002e710a5e1c55
Autor:
Radlović Nedeljko, Mladenović Marija, Leković Zoran, Živanović Dragana, Brdar Radivoj, Radlović Vladimir, Ristić Dragana, Pavlović Momčilo, Stojšić Zorica, Vuletić Biljana, Đurđević Jelena, Gajić Milan
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 137, Iss 11-12, Pp 632-637 (2009)
Introduction. Gluten-free diet (GFD) presents the basis of coeliac disease (CD) treatment. If strictly applied, the disorders of the small bowel mucosa and other disease signs rapidly resolve. Objective. The goal of the study was to evaluate the effe
Externí odkaz:
https://doaj.org/article/75b7c469af9145e79d4fe592e2f085b4
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 137, Iss 9-10, Pp 554-557 (2009)
Introduction Pyogenic infection of sacroiliac joint (SIJ) is very rare in children. It is the result of haematogenous spread primarily affecting the joint. The process is usually monoarticular. By rule, sequestra are rarely formed, there are no great
Externí odkaz:
https://doaj.org/article/bd10a92ab2724b4e84b2e7daf9083703
Autor:
Rakonjac Zoran, Brdar Radivoj
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 137, Iss 3-4, Pp 179-184 (2009)
Introduction. The fracture of the external condyle is the most common fracture of the distal end of the humerus. This is an intraarticular fracture, which, if not properly treated, can cause serious complications, difficult to treat. Objective. To de
Externí odkaz:
https://doaj.org/article/9e8e339b21d942fab4b3bca58a3475b8
Autor:
Ćirović Dragana, Petronić Ivana, Nikolić Dejan, Brdar Radivoj, Pavićević Polina, Knežević Tatjana
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 137, Iss 9-10, Pp 502-505 (2009)
Introduction Neurogenic bladder can develop as a result of various degrees of neurogenic lesion in spina bifida. The degree of bladder dysfunction depends on the level and type of spina bifida. Due to results upon complete diagnostic protocols, treat
Externí odkaz:
https://doaj.org/article/00992b872fe14daa97694a506bf04df5
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 136, Iss 9-10, Pp 514-518 (2008)
INTRODUCTION Langerhans cell histiocytosis is a rare disease in children, initial presentation is variable, clinical course, prognosis and survival are mostly unpredictable. OBJECTIVE To summarise clinical characteristics and treatment results in chi
Externí odkaz:
https://doaj.org/article/d4bb8d9117cd4b30b2b7b9650c67302a
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