Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Štefan Blazina"'
Autor:
Sonja Ota, Nataša Toplak, Tina Vesel Tajnšek, Anja Koren Jeverica, Gašper Markelj, Štefan Blazina, Vlasta Dragoš, Manca Tekavčič Pompe, Tanja Tomaževič, Tadej Avčin
Publikováno v:
Zdravniški Vestnik, Vol 91, Iss 5-6, Pp 196-204 (2022)
Stevens-Johnsonov sindrom (SJS) in toksična epidermalna nekroliza (TEN) sta redki življenje ogrožajoči bolezni, ki se kažeta z nastajanjem mehurjev ter odstopanjem povrhnjice kože in sluznic. Najpogosteje sta posledica imunsko sprožene reakcij
Externí odkaz:
https://doaj.org/article/74491d1e66034fb48b1b244269042c8a
Publikováno v:
Slovenska pediatrija, Vol 28, Iss 1, Pp 24-29 (2021)
Koprivnica je v otroškem obdobju pogosta bolezen, za katero je značilno pojavljanje prehodnih srbečih koprivk, ki jih lahko spremlja angioedem. V večini primerov se koprivke nehajo pojavljati v nekaj dneh ali tednih, občasno pa koprivnica traja
Externí odkaz:
https://doaj.org/article/5c0585a9dd7f4027b5d084b26e2a0baf
Publikováno v:
Slovenska pediatrija, Vol 28, Iss 1, Pp 24-29 (2021)
Urticaria is a common disease in childhood, characterised by the appearance of a transient itchy nettle rash on the skin, which may be accompanied by angioedema. In most cases, the rash stops appearing within a few days or weeks, but occasionally it
Externí odkaz:
https://doaj.org/article/fbb211ac463b4269b51a65e5316ad12e
Autor:
Andreja N. Kopitar, Gašper Markelj, Miha Oražem, Štefan Blazina, Tadej Avčin, Alojz Ihan, Maruša Debeljak
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Actin nucleators initiate formation of actin filaments. Among them, the Arp2/3 complex has the ability to form branched actin networks. This complex is regulated by members of the Wiscott-Aldrich syndrome protein (WASp) family. Polymerization of acti
Externí odkaz:
https://doaj.org/article/81884a82dc6d4c03894fbebdfcbbc5cd
Autor:
Štefan Blazina, Maruša Debeljak, Mitja Košnik, Saša Simčič, Sanja Stopinšek, Gašper Markelj, Nataša Toplak, Peter Kopač, Breda Zakotnik, Marko Pokorn, Tadej Avčin
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
BackgroundPrevalence of complement deficiencies (CDs) is markedly higher in Slovenian primary immunodeficiency (PID) registry in comparison to other national and international PID registries.ObjectiveThe purposes of our study were to confirm CD and d
Externí odkaz:
https://doaj.org/article/cc226a84b9034c5ba935e5f6ca120a94
Autor:
Tadej Avčin, Tanja Tomaževič, Manca Tekavčič Pompe, Vlasta Dragoš, Štefan Blazina, Gašper Markelj, Anja Koren Jeverica, Tina Vesel Tajnšek, Nataša Toplak, Sonja Ota
Publikováno v:
Slovenian Medical Journal. :1-9
Stevens-Johnsonov sindrom (SJS) in toksična epidermalna nekroliza (TEN) sta redki življenje ogrožajoči bolezni, ki se kažeta z nastajanjem mehurjev ter odstopanjem povrhnjice kože in sluznic. Najpogosteje sta posledica imunsko sprožene reakcij
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00100219f6b6f330ce84487754497cc1
https://doi.org/10.6016/zdravvestn.3058
https://doi.org/10.6016/zdravvestn.3058
Publikováno v:
Drug Design, Development and Therapy. 12:1633-1643
The pathogenesis, clinical course, and response to treatment in systemic juvenile idiopathic arthritis (SJIA) differ from other types of juvenile idiopathic arthritis and are similar to other interleukin-1 (IL-1)-mediated diseases. The main cytokine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dabe20997a75cd781b71b30e112a3fc
https://doi.org/10.2147/dddt.s114532
https://doi.org/10.2147/dddt.s114532
Publikováno v:
Abstracts Accepted for Publication.
Background The symptoms of pediatric Sjogren’s syndrome (SS) are different than in adults. There are currently no validated pediatric diagnostic criteria or treatment guidelines for SS. In most cases adult criteria are used, but they apply poorly t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc75514b82989b86a7acbff4b42d6ecb
https://doi.org/10.1136/annrheumdis-2019-eular.3817
https://doi.org/10.1136/annrheumdis-2019-eular.3817
Autor:
Maša, Bizjak, Štefan, Blazina, Mojca, Zajc Avramovič, Gašper, Markelj, Tadej, Avčin, Nataša, Toplak
Publikováno v:
Clinical and experimental rheumatology. 38(1)
To assess vaccination status in a cohort of children with rheumatic diseases followed at the University Children's Hospital Ljubljana and to evaluate the most common reasons for vaccination dropout.Patients with rheumatic diseases who were evaluated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4aad9837fc6f30e9159ae92d2a7bbad4
https://pubmed.ncbi.nlm.nih.gov/31577215
https://pubmed.ncbi.nlm.nih.gov/31577215
Publikováno v:
American Journal of Medical Genetics Part A. 170:3237-3240
Antibody deficiency is common finding in patients with Jacobsen syndrome (JS). In addition, there have been few reports of T-cell defects in this condition, possibly because most of the reported patients have not been specifically evaluated for T-cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fa8fb44672eca62a24157a5f5e36a0e
https://doi.org/10.1002/ajmg.a.37859
https://doi.org/10.1002/ajmg.a.37859