Zobrazeno 1 - 3
of 3
pro vyhledávání: '"non-Langerhans cell histiocytosi"'
Autor:
Emilio Berti, Arturo Bonometti, Carlo Cavaliere, Massimo Marano, Emanuela Passoni, Augusto Vaglio, Mario Cirillo, Antonio Todisco, Giovanni Cirillo
Publikováno v:
Clinical Neurology and Neurosurgery. 194:105841
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::907e6cd4c259f5c252d0273b1112b067
https://doi.org/10.1016/j.clineuro.2020.105841
https://doi.org/10.1016/j.clineuro.2020.105841
Autor:
B. Guglielmi, Alessandro Tomelleri, Giulio Cavalli, Alvise Berti, Corrado Campochiaro, Roberto Nicoletti, Andrea Panzacchi, Riccardo Biavasco, Lorenzo Dagna, Marina Ferrarini
Publikováno v:
OncoImmunology, Vol 6, Iss 6 (2017)
Treatment of ErdheimâChester disease (ECD), a rare non-Langerhans histiocytosis, relies on interferon-α, chemotherapeutic agents such as purine analogs, cytokine-blocking agents and BRAF inhibitors. Since interleukin (IL)-6 levels are elevate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba80861394ec163d316a6de51ff15dc1
https://www.tandfonline.com/doi/full/10.1080/2162402X.2017.1318237
https://www.tandfonline.com/doi/full/10.1080/2162402X.2017.1318237
Autor:
Giuseppe Brunori, Lydia Giannitrapani, Antonietta Serruto, Francesco Bencivinni, Aurelio Seidita, Maurizio Soresi
Publikováno v:
Italian Journal of Medicine, Vol 11, Iss 1, Pp 64-70 (2016)
Erdheim-Chester disease is a rare non-Langerhans cell histiocytosis with multiorgan involvement and a specific tropism for perivascular and fatty connective tissue, of unclear origin, with poor response to therapy. Its identification is difficult bec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e4930642fdf4cfaf12b2f75f5f68b79
https://doi.org/10.4081/itjm.2016.700
https://doi.org/10.4081/itjm.2016.700