Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mirjana Stojsic"'
Autor:
Borko Milanović, Gordana Vijatov-Djuric, Mirjana Stojsic, Jelena Stojcevic-Maletic, Aleksandra Milutinović
Publikováno v:
Medical review. 73:88-93
Introduction. Recent studies point to the importance of interleukin-33 in the pathogenesis of allergic respiratory diseases. The relationship of interleukin-33 and certain allergic respiratory diseases as well as their characteristics is not fully el
Publikováno v:
Srpski arhiv za celokupno lekarstvo. :48-48
Introduction. Short bowel syndrome in children is a rare disease. One of the most common etiological factors for the development of short bowel syndrome in children is atresia of the small intestine. After surgical correction of the congenital anomal
Autor:
Cila Demesi-Drljan, Natasa Nenadov, Aleksandra Mikov, Jelena Zvekic-Svorcan, Mirjana Stojsic, Maja Radovanov, Rastislava Krasnik
Publikováno v:
Vojnosanitetski Pregled, Vol 76, Iss 5, Pp 485-491 (2019)
Background/Aim. Children with cerebral palsy (CP) grow at a slower rate relative to their peers. Their body height, body weight and bone mineral density are significantly below those measured for healthy children of corresponding age. The aim of this
Autor:
Mirjana Stojsic, Jelena Ilic-Sabo, Mirjana Zivojinov, Tatiana Jocić, Olgica Latinovic-Bosnjak
Publikováno v:
Vojnosanitetski Pregled, Vol 75, Iss 1, Pp 95-99 (2018)
Introduction. Primary intestinal lymphangiectasia is a rare disorder, characterized by abnormal dilation of intestinal lymphatic vessels and extensive enteric loss of lymph rich in plasma proteins, lymphocytes and chylomicrons. The main characteristi
Autor:
Ivana Fratrić, Jelena Antić, Mirjana Stojsic, Svetlana Bukarica, Radoica Jokić, Aleksandar Komarcevic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 145, Iss 7-8, Pp 403-406 (2017)
Introduction. Trichobezoars and gastric polyps are very rare conditions in children and may pose a diagnostic and therapeutic challenge. The purpose of this work is to present our successful experience using combined laparoscopic-endoscopic procedure
Autor:
Anastazija Stojsic-Milosavljevic, Mirjana Stojsic, Artur Bjelica, Radojica Savic, Miloš Pajić, Gordana Vijatov-Djuric, Djerdji Erdes-Kavecan, Jasmina Katanic, Ivana Kavecan, Helena Hrnjak Ilic, Tatjana Redzek Mudrinic, Nada Vuckovic, Gordana Velisavljev Filipovic
Publikováno v:
Iranian Red Crescent Medical Journal. 20
Introduction: Pachydermodactyly is a very rare type of macrodactyly. It clinically resembles juvenile rheumatoid arthritis, but it has a non-inflammatory etiology without bone, articular, or synovial involvement. Case Presentation: In this study, we