Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Zeljko Smoljanic"'
Autor:
Zeljko Smoljanic, Polina Pavicevic, Zoran Lekovic, Nedeljko Radlovic, Sinisa Ducic, Vladimir Radlovic, Dragana Ristic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 142, Iss 1-2, Pp 75-78 (2014)
Introduction. X-linked hypophosphatemic rickets (XLHR) is a dominant inherited disease caused by isolated renal phosphate wasting and impairment of vitamin D activation. We present a girl with X-linked hypophosphatemic rickets (XLHR) as a consequence
Autor:
Zoran Radojicic, Aleksandar Janjic, Sinisa Ducic, Nenad Janic, Sava V. Perovic, Vojkan Vukadinovic, Polina Pavićević, Zeljko Smoljanic
Publikováno v:
BJU International. 108:1660-1663
OBJECTIVE To present outcomes of a minimally invasive inguinal technique for the separation of the distal part of ureters in duplex systems and for the extravesical ureteroneocystostomy of only the pathologically involved ureter. MATERIALS AND METHOD
Autor:
Zoran Lekovic, Radivoj Brdar, Miodrag Jovanovic, Zeljko Smoljanic, Dragana Ristic, Lidija Dokmanovic, Nenad Janic, Nedeljko Radlovic, Dragana Janic
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-
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 136, Iss 11-12, Pp 603-608 (2008)
INTRODUCTION Hepatoblastoma is the most frequent malignant liver tumour of childhood and it accounts for 1% of all paediatric cancers. The outcome is significantly improved by introducing intensive chemotherapy regimens followed by complete surgical
Autor:
Dragana Janic, Zeljko Smoljanic, Nada Jovanovic, Dimitrije Brasanac, Predrag Rodic, Lidija Dokmanovic, Jelena Lazic
Publikováno v:
Pediatric Hematology and Oncology. 24:141-148
The authors describe a male infant with a history of transient pancytopenia who developed progressive bilateral proptosis associated with diffuse infiltration of the kidney and normal bone marrow. The histopathological examination of the kidney revea
Autor:
Branislava Keserovic, Borko Stojanovic, Miroslav L. Djordjevic, Stojan M. Zivkovic, Goran Djuricic, Zeljko Smoljanic, Polina Pavicevic, Natasa Milic
Publikováno v:
Annals of Pediatric Surgery
Annals of Pediatric Surgery; Vol 11, No 3 (2015); 173-180
Annals of Pediatric Surgery; Vol 11, No 3 (2015); 173-180
Objective This retrospective study was designed to assess and compare the anatomical, functional, and esthetic appearance of the umbilical area in patients after repair of gastroschisis using the inner surface of the umbilical cord (UC) and in patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::169e36d0938c308be93f3aced9cb0bdf
http://intor.torlakinstitut.com/handle/123456789/437
http://intor.torlakinstitut.com/handle/123456789/437
Autor:
Radoslav Lukac, Zeljko Smoljanic, Zoran Krstic, Dragana Vujovic, Marija Lukac, Polina Pavicevic, Svjetlana Maglajlić, Sanja Sindjic, Aleksandar Ljubic
Publikováno v:
Srpski arhiv za celokupno lekarstvo. 132:77-81
Prenatal diagnosis allows for insight into the evaluation of fetal lung anomalies. Serial ultrasonographic studies of fetuses helped in evaluation and definition of the natural course of these lesions as well as necessity for fetal therapy. It has be
Publikováno v:
Pediatric Surgery International. 17:329-333
From 1989-1998 14 patients were treated with cloacal anomalies: 5 typical cloacas (PC), 5 posterior cloacas, and 4 cloacal exstrophies (CE); 12 underwent surgery. Four typical cloacas were resolved with posterior sagittal anorectovagino-urethroplasty
Publikováno v:
Pediatric Surgery International. 16:580-583
True hermaphroditism (TH) is the rarest variant of intersex malformations. By definition, these patients have both ovarian and testicular tissue. Most present due to ambiguous genitalia and/or gynecomastia. From 1986 to 1996, we treated 97 patients w
Publikováno v:
International Journal of Hematology. 89:201-203
We report on a 17-year-old patient with severe hemophilia A without inhibitors who developed abdominal bleeding after an episode of severe cough. Abdominal ultrasound showed intramural intestinal hematoma as well as large amount of peritoneal fluid a