Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Dušan Trpinac"'
Autor:
Snežana Minić, Nataša Cerovac, Ivana Novaković, Slobodan Gazikalović, Svetlana Popadić, Dušan Trpinac
Publikováno v:
Diagnostics, Vol 13, Iss 7, p 1300 (2023)
Incontinentia pigmenti (IP) is a rare skin disease combined with anomalies of the teeth, eyes, and central nervous system (CNS). Mutations of the IKBKG gene are responsible for IP. Among the most frequent CNS abnormalities found in IP using magnetic
Externí odkaz:
https://doaj.org/article/581be68129d3486197b88ad4ca2d5e9d
Autor:
Snežana Minić, Dušan Trpinac, Ivana Novaković, Nataša Cerovac, Danijela Dobrosavljević Vukojević, Jérémie Rosain
Publikováno v:
Diagnostics, Vol 12, Iss 7, p 1711 (2022)
Rare diseases represent a diagnostic challenge due to their number, variety of clinical phenomena, and possibility of a simultaneous presence of two or more diseases. An illustration of this challenge is an occurrence of a late diagnosis of a proband
Externí odkaz:
https://doaj.org/article/995e8b2ab52341f284c9c159dd9bb147
Autor:
Vladimir Bumbasirevic, Jelena Bila, Darko Ciric, Tamara Kravic-Stevovic, Tamara Martinovic, Olivera Markovic, Dušan Trpinac, Dragomir Marisavljevic, V. Cemerikic-Martinovic
Publikováno v:
Vojnosanitetski Pregled, Vol 76, Iss 7, Pp 740-744 (2019)
Introduction. Congenital asplenia is an extremely rare condition that can be separate entity due to a specific defect of spleen development or may occur in the context of a malformation syndrome. The patients with asplenia have thrombocytosis and sus
Publikováno v:
Medical Hypotheses. 81:671-674
In X-chromosome-linked skin disorders the pattern of involvement follows Blaschko lines. Patterns of changes analogous to cutaneous Blaschko lines in different X-linked diseases existed in other organs. There is no commonly accepted analogy to Blasch
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 143, Iss 11-12, Pp 752-754 (2015)
Introduction. Incontinentia pigmenti (IP) is a rare X-linked dominant genodermatosis. Mutations of the IKBKG gene are responsible for IP. A deletion of exons 4-10 can be found in 80% of patients with IP. There are 69 different mutations of the IKBKG
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 141, Iss 7-8, Pp 490-494 (2013)
SUMMARY Introduction Incontinentia pigmenti (IP) is a rare X-linked dominant genodermatosis. Mutations of the IKBKG gene are the only known cause of IP. The presence of other than skin changes is important in the diagnosis of atypical IP cases when s
Autor:
Dušan Trpinac, Slobodan Krstic, Jasna Trbojevic, Z. Lausevic, Biljana Stojimirov, Natasa Jovanovic, Snezana Zunic-Bozi
Publikováno v:
Journal of Animal and Veterinary Advances. 10:1414-1420
Autor:
Z. Lausevic, Vesna Cemerikic-Martinovic, Dušan Trpinac, Jasna Trbojević-Stanković, Biljana Stojimirovic, Miljana Obradović
Publikováno v:
Vojnosanitetski Pregled, Vol 68, Iss 7, Pp 556-560 (2011)
Background/Aim. During peritoneal dialysis (PD) an exchange of substances between blood and dialysate takes place through specific histological structures of peritoneum. Peritoneal double-layered serous membrane has, so far, mostly been studied with
Autor:
Gerd E K Novotnyt, Miljana Obradović, Snezana Minic, Ljiljana Medenica, Dušan Trpinac, Bratislav D. Stefanović
Publikováno v:
Vojnosanitetski Pregled, Vol 67, Iss 2, Pp 183-186 (2010)
Background. Incontinentia pigmenti (IP) is a rare, complex, X-linked genodermatosis in which skin changes are combined with defects of other organs. It appears almost exclusively in females and is usually lethal in men. It is estimated that according
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 138, Iss 7-8, Pp 408-413 (2010)
Introduction. Incontinentia pigmenti (IP) is an X-linked genodermatosis in which skin changes are combined with dental, eye and central nervous system anomalies. Objective. The goal of the study was to analyze ocular findings, IP minor criteria in av