Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Dusan Trpinac"'
Publikováno v:
Dermatology Practical & Conceptual, Vol 12, Iss 3 (2022)
Introduction: Incontinentia pigmenti (IP) is a rare X-linked geno-dermatosis characterized by numerous findings. Skin biopsy and histopathological analysis are considered as minor criteria for the diagnosis of IP. We assume that dermoscopy can assist
Externí odkaz:
https://doaj.org/article/998f94c31b094a858c60461e0be64916
Autor:
Natasa Jovanovic, Snezana Zunic-Bozinovski, Dusan Trpinac, Zeljko Lausevic, Slobodan Krstic, Dejan Opric, Jasna Trbojevic-Stankovic, Biljana Stojimirovic
Publikováno v:
Vojnosanitetski Pregled, Vol 70, Iss 11, Pp 1023-1028 (2013)
Background/Aim. The number of patients with end-stage renal diseases treated with chronic dialysis is increasing over the last years. Long-term peritoneal dialysis is associated with progressive development of structural and functional alterations of
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