Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Snezana Minic"'
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
Publikováno v:
Family Practice.
Background Acne vulgaris is one of the most frequent visits to primary care physicians and dermatologists alike. Isotretinoin is the backbone of acne treatment. In most countries, depending on the health care system, isotretinoin is prescribed by der
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3da7ee3af2a4b2cb73054170ade9743e
https://doi.org/10.1093/fampra/cmad043
https://doi.org/10.1093/fampra/cmad043
Publikováno v:
Australasian Journal of Dermatology. 64
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1831ee8f48ba79384bf1268084df40b4
https://doi.org/10.1111/ajd.13997
https://doi.org/10.1111/ajd.13997
Autor:
Nada Santrac, Snezana Minic, Vesna Lackovic, Stevan Jokic, Marko Buta, Milan Gajic, Zelimir Jovanovic, Aleksandar Martinovic
Publikováno v:
Archives of Biological Sciences, Vol 67, Iss 3, Pp 935-940 (2015)
The aim of this study was to establish whether older patients with skin melanoma (in an analyzed group of 189 patients treated at the Institute for Oncology and Radiology of Serbia from 2004 to 2008), have worse survival compared to younger patients.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c20c446e80f6eb0f93d3915463c653b6
http://www.doiserbia.nb.rs/img/doi/0354-4664/2015/0354-46641500055M.pdf
http://www.doiserbia.nb.rs/img/doi/0354-4664/2015/0354-46641500055M.pdf
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebb2745a89d52fa751dd02eae9134ed1
http://www.doiserbia.nb.rs/img/doi/0370-8179/2013/0370-81791308490M.pdf
http://www.doiserbia.nb.rs/img/doi/0370-8179/2013/0370-81791308490M.pdf
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::adacfe4a46c470a7b1d1a9a1d8b6687b
http://www.doiserbia.nb.rs/img/doi/0042-8450/2010/0042-84501002183M.pdf
http://www.doiserbia.nb.rs/img/doi/0042-8450/2010/0042-84501002183M.pdf
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98af3d14db5cd6fc2fb229224cf16108
http://www.doiserbia.nb.rs/img/doi/0370-8179/2010/0370-81791008408M.pdf
http://www.doiserbia.nb.rs/img/doi/0370-8179/2010/0370-81791008408M.pdf
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