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pro vyhledávání: '"Langerhans cell histiocytosi"'
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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:
R. Maarten Egeler, Paul J. Orchard, Mary Eapen, Giuseppe Bandini, Paul Veys, Jeffrey H. Davis, Susanne Matthes, Gretchen Eames, Olle Ringdén, K. Scott Baker, Herbert Jürgens, Alexandra H. Filipovich, Paul G. Schlegel, Vasanta Nanduri, Anna Pieczonka, Alain Fischer, Wing Leung, Anne Sirvent, Andrea Biondi, Robert A. Krance, Edoardo Lanino, Wensheng He, Gérard Michel, Kim Vettenranta, Arnaud Dalissier
Publikováno v:
British Journal of Haematology. 169:711-718
Patients with Langerhans cell histiocytosis (LCH) refractory to conventional chemotherapy have a poor outcome. There are currently two promising treatment strategies for high-risk patients: the first involves the combination of 2-chlorodeoxyadenosine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed88ba1409845b835ee0056a7dcc1f44
https://doi.org/10.1111/bjh.13347
https://doi.org/10.1111/bjh.13347
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
Autor:
Elisabetta Alafaci, Francesco M. Salpietro, Francesca Granata, Rosa Morabito, Concetta Alafaci, Giovanni Grasso
Publikováno v:
Surgical Neurology International
Background: Langerhans cell histiocytosis (LCH) is a rare disease involving clonal proliferation of cells with characteristics similar to bone marrow-derived Langerhans cells. The case of a young woman, affected by Turner syndrome and a solitary intr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::400f6d13041e208d4e0ccb704c16d695
https://doi.org/10.4103/2152-7806.179429
https://doi.org/10.4103/2152-7806.179429
Publikováno v:
Scopus-Elsevier
Langerhans cell histiocytosis (LCH) may be a single-system disease or a multisystem disease with organ dysfunction. Cytotoxic drugs and corticosteroids, alone or in combination, are the treatments for multisystem LCH. We report the case of a young gi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cd2cc4a142da9700d70c4c7220e415e8
http://hdl.handle.net/11585/110788
http://hdl.handle.net/11585/110788
Autor:
GUIGLIA, Rosario, PIZZO, Giuseppe, MARESI, Emiliano, COMPILATO, Domenico, CAMPISI, Giuseppina, ARICO', M
Background: Eosinophilic granuloma (EG) is a clinical variant of the Langerhans cell histiocytosis (LCH) characterized by unifocal or multifocal bone lesions which predominantly affects children, adolescents, and young adults. Case Report: A case is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::10a023821837f64ce4520633dff5478c
http://hdl.handle.net/10447/37680
http://hdl.handle.net/10447/37680
Publikováno v:
Scopus-Elsevier
BACKGROUND: Pulmonary Langerhans cell histiocytosis (PLCH) is an interstitial lung disease characterized by bilateral nodular and cystic lesions. Clinically it seems to be a reactive process related to cigarette smoking. CASES: In 2 cases of PLCH, cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::352cba829d7c2456393ff4e8de4c58c4
http://hdl.handle.net/11386/3104760
http://hdl.handle.net/11386/3104760
Autor:
Bartolomeo Merola, Gaetano Lombardi, Antonio Bellastella, G. Lodice, A. Colao, A. Bizzarro, A. De Bellis, N. Panza
Publikováno v:
Scopus-Elsevier
Two cases of Langerhans cell histiocytosis (LCH) expressing as Hand-Schuller-Christian syndrome with diabetes insipidus, hyperprolactinemia and empty sella are here reported. Up-to-date this four-fold association is lacking in world literature and it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75c31c2d4633358ac1755a52e7b110d1
https://pubmed.ncbi.nlm.nih.gov/8851691
https://pubmed.ncbi.nlm.nih.gov/8851691