Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Irina Stoia Djeska"'
Autor:
Irina Stoia Djeska, Anca Maria Cimpean, Alexandru Nicodin, Marius Raica, Voicu Tudorache, Raluca Amalia Ceausu, O. Mederle, Pusa Nela Gaje
Publikováno v:
Archives of Biological Sciences, Vol 65, Iss 4, Pp 1599-1604 (2013)
The aspect of reticular fibers is not considered in the current classifications of lung fibrosis. The aim of our study was to evaluate the distribution and the architecture of the reticular fibers for potential use as a tissue marker of fibrosis seve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfe062e909e88f7de0ba5232e1acacf6
https://doi.org/10.2298/abs1304599d
https://doi.org/10.2298/abs1304599d
Publikováno v:
Journal of Drug Assessment
Objectives The aim of this study was to analyze the performance of the tuberculin skin test (TST) for screening and monitoring patients treated with anti-tumor necrosis factor agents, in a high-incidence area. Methods A 3-year retrospective study was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5ad7bf770dd75dfb9f0e5dbdab79351
https://doi.org/10.3109/21556660.2012.744315
https://doi.org/10.3109/21556660.2012.744315
Autor:
Pusa Nela, Gaje, Irina, Stoia-Djeska, Anca Maria, Cimpean, Raluca Amalia, Ceausu, Voicu, Tudorache, Marius, Raica
Publikováno v:
In vivo (Athens, Greece). 28(3)
Despite increasing knowledge on the cellular and molecular mechanisms involved in pulmonary fibrosis, its therapeutic options are still limited. The study of lymphangiogenesis has contributed to a better understanding of tumor growth and metastasis,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f7bc0a6de5b1453e9eda70ea213c8a2c
https://pubmed.ncbi.nlm.nih.gov/24815840
https://pubmed.ncbi.nlm.nih.gov/24815840
Autor:
Irina, Stoia-Djeska, Raluca Amalia, Ceauşu, Anca Maria, Cîmpean, A, Nicodin, V, Tudorache, M, Raica
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 54(1)
Idiopathic pulmonary fibrosis is a severe disease, with unpredictable evolution that frequently leads to respiratory failure and death, despite some progresses made in the field of therapy. Basically, the bad prognosis and failure of therapy are the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e0c304addb8e4a82fa732da8c8005a77
https://pubmed.ncbi.nlm.nih.gov/23529310
https://pubmed.ncbi.nlm.nih.gov/23529310