Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Elena Sieni, ∗"'
Autor:
Irene Trambusti, Carmen Barba, Marzia Mortilla, Susanna Rizzi, Katiuscia Romano, Maria Luisa Coniglio, Ersilia Lucenteforte, Annalisa Tondo, Renzo Guerrini, Elena Sieni
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
AimsEarly detection and treatment of neurodegenerative Langerhans cell histiocytosis (ND-LCH) have been suggested to prevent neurodegenerative progression. The aim of the study is to validate a standardized multidisciplinary diagnostic work-up to mon
Externí odkaz:
https://doaj.org/article/fada1ee409374047897c7a03fe029e09
Autor:
Francesco Pegoraro, Matthias Papo, Fleur Cohen-Aubart, Francesco Peyronel, Gianmarco Lugli, Irene Trambusti, Gildas Baulier, Mathilde de Menthon, Tanguy Le Scornet, Eric Oziol, Nicole Ferreira-Maldent, Olivier Hermine, Benoit Faucher, Dirk Koschel, Nicole Straetmans, Noémie Abisror, Benjamin Terrier, François Lifermann, Jerome Razanamahery, Yves Allenbach, Jeremy Keraen, Sophie Bulifon, Baptiste Hervier, Annamaria Buccoliero, Frederic Charlotte, Quentin Monzani, Samia Boussouar, Natalia Shor, Annalisa Tondo, Stephane Barete, Ahmed Idbaih, Abdellatif Tazi, Elena Sieni, Zahir Amoura, Jean-François Emile, Augusto Vaglio, Julien Haroche
Publikováno v:
EClinicalMedicine, Vol 73, Iss , Pp 102658- (2024)
Summary: Background: Erdheim-Chester disease (ECD) is a rare histiocytosis that may overlap with Langerhans Cell Histiocytosis (LCH). This “mixed” entity is poorly characterized. We here investigated the clinical phenotype, outcome, and prognosti
Externí odkaz:
https://doaj.org/article/c0be6220792e41cd85b59cd24505dcd6
Autor:
Silvia Ricci, Walter Maria Sarli, Lorenzo Lodi, Clementina Canessa, Francesca Lippi, Donata Dini, Marta Ferrari, Laura Pisano, Elena Sieni, Giuseppe Indolfi, Massimo Resti, Chiara Azzari
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/ada3ae997b1b4c85bf5ff4fa6b65821b
Autor:
Francesco Pegoraro, Aurora Chinnici, Linda Beneforti, Michele Tanturli, Irene Trambusti, Carmela De Fusco, Concetta Micalizzi, Veronica Barat, Simone Cesaro, Stefania Gaspari, Fabiola Dell’Acqua, Alessandra Todesco, Fabio Timeus, Maurizio Aricò, Claudio Favre, Annalisa Tondo, Maria Luisa Coniglio, Elena Sieni, AIEOP Histiocytosis Working Group
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
Primary hemophagocytic lymphohistiocytosis (pHLH) is a severe, life-threatening hyperinflammatory syndrome caused by defects in genes of the granule-dependent cytotoxic pathway. Here we investigated the clinical presentation and outcome in a large
Externí odkaz:
https://doaj.org/article/a8dd69a4db024b2788b7c5b238c97b72
Autor:
Silvia Ricci, Walter Maria Sarli, Lorenzo Lodi, Clementina Canessa, Francesca Lippi, Donata Dini, Marta Ferrari, Laura Pisano, Elena Sieni, Giuseppe Indolfi, Massimo Resti, Chiara Azzari
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
BackgroundHemophagocytic Lymphohistiocytosis (HLH) is a rare and life-threatening condition characterized by a severe impairment of the immune homeostasis. While Familial-HLH (FHL) is a known cause, the involvement of other Inborn Errors of Immunity
Externí odkaz:
https://doaj.org/article/1110d30671e84a5a9bd9df857062c014
Autor:
Francesco Pegoraro, Aurora Chinnici, Linda Beneforti, Michele Tantuli, Irene Trambusti, Carmen De Fusco, Concetta Micalizzi, Alessandra Todesco, Fabiola Dell’acqua, Stefania Gaspari, Maria Luisa Coniglio, Elena Sieni
Publikováno v:
HemaSphere, Vol 7, p e62871f1 (2023)
Externí odkaz:
https://doaj.org/article/67f5d3e0d3f9442fa533351249d9fc2e
Autor:
Francesco Pegoraro, Martina Mazzariol, Irene Trambusti, Saamer Bakhshi, Saumyaranjan Mallick, Ira J. Dunkel, Van den Bos Cor, Ozlem Tezol, Shijun Shan, Suheyla Ocak, Flavio Giordano, Carmen De Fusco, Stefania Gaspari, Jean Donadieu, Eli Diamond, Jean-Francois Emile, Elena Sieni, Julien Haroche, Augusto Vaglio
Publikováno v:
HemaSphere, Vol 7, p e44200f4 (2023)
Externí odkaz:
https://doaj.org/article/239ca57cd85743fabf7d95809c7923ad
Autor:
Elena Sophia Fratini, Maddalena Migliavacca, Federica Barzaghi, Claudia Fossati, Stefania Giannelli, Ilaria Monti, Miriam Casiraghi, Francesca Ferrua, Salvatore Recupero, Giulia Consiglieri, Valeria Calbi, Francesca Tucci, Vera Gallo, Maria Ester Bernardo, Sabina Cenciarelli, Monica Palmoni, Margherita Moni, Luca Galimberti, Marzia Duse, Lucia Leonardi, Elena Sieni, Elena Soncini, Fulvio Porta, Lucia Dora Notarangelo, Raffaella De Santis, Saverio Ladogana, Alessandro Aiuti, Maria Pia Cicalese
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Hemophagocytic inflammatory syndrome (HIS) is a rare form of secondary hemophagocytic lymphohistiocytosis caused by an impaired equilibrium between natural killer and cytotoxic T-cell activity, evolving in hypercytokinemia and multiorgan failure. In
Externí odkaz:
https://doaj.org/article/7c36f84d68d64741ac3146f248b26d26
Autor:
Aurora Chinnici, Linda Beneforti, Francesco Pegoraro, Irene Trambusti, Annalisa Tondo, Claudio Favre, Maria Luisa Coniglio, Elena Sieni
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Hemophagocytic Lymphohistiocytosis (HLH) is a rare clinical condition characterized by sustained but ineffective immune system activation, leading to severe and systemic hyperinflammation. It may occur as a genetic or sporadic condition, often trigge
Externí odkaz:
https://doaj.org/article/e5416618a7cb4444a24e60c4681541a3
Autor:
Paul G. Kemps, Timo C. E. Zondag, Helga B. Arnardóttir, Nienke Solleveld-Westerink, Jelske Borst, Eline C. Steenwijk, Demi van Egmond, Joost F. Swennenhuis, Ellen Stelloo, Irene Trambusti, Robert M. Verdijk, Carel J. M. van Noesel, Arjen H. G. Cleven, Marijn A. Scheijde-Vermeulen, Marco J. Koudijs, Lenka Krsková, Cynthia Hawkins, R. Maarten Egeler, Jesper Brok, Tatiana von Bahr Greenwood, Karel Svojgr, Auke Beishuizen, Jan A. M. van Laar, Ulrike Pötschger, Caroline Hutter, Elena Sieni, Milen Minkov, Oussama Abla, Tom van Wezel, Cor van den Bos, Astrid G. S. van Halteren
Publikováno v:
Blood advances, 7(4), 664-679. American Society of Hematology
Langerhans cell histiocytosis (LCH) is a rare neoplastic disorder caused by somatic genetic alterations in hematopoietic precursor cells differentiating into CD1a+/CD207+ histiocytes. LCH clinical manifestation is highly heterogeneous. BRAF and MAP2K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af8313baedb40f4a65321041d0cf2628
https://doi.org/10.1182/bloodadvances.2022007947
https://doi.org/10.1182/bloodadvances.2022007947