Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Annalisa, Tondo"'
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:
Nicolò Peccatori, Elena Chiocca, Valentino Conter, Annalisa Tondo, Matilde Marzorati, Tommaso Casini, Marinella Veltroni, Andrea Biondi, Grazia Fazio
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
The incorporation of tyrosine kinase inhibitors (TKIs) in the treatment of Philadelphia chromosome–positive acute lymphoblastic leukemia (Ph+ ALL) led to significant improvement. However, in the pediatric setting, the outcomes of Ph+ ALL are still
Externí odkaz:
https://doaj.org/article/7dc7ab054a7c4175927a16d31aa0a302
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:
Mario Capasso, Chiara Brignole, Vito A. Lasorsa, Veronica Bensa, Sueva Cantalupo, Enrico Sebastiani, Alessandro Quattrone, Eleonora Ciampi, Marianna Avitabile, Angela R. Sementa, Katia Mazzocco, Barbara Cafferata, Gabriele Gaggero, Valerio G. Vellone, Michele Cilli, Enzo Calarco, Elena Giusto, Patrizia Perri, Sanja Aveic, Doriana Fruci, Annalisa Tondo, Roberto Luksch, Rossella Mura, Marco Rabusin, Francesco De Leonardis, Monica Cellini, Paola Coccia, Achille Iolascon, Maria V. Corrias, Massimo Conte, Alberto Garaventa, Loredana Amoroso, Mirco Ponzoni, Fabio Pastorino
Publikováno v:
Journal of Translational Medicine, Vol 22, Iss 1, Pp 1-20 (2024)
Abstract Background Neuroblastoma (NB) represents the most frequent and aggressive form of extracranial solid tumor of infants. Although the overall survival of patients with NB has improved in the last years, more than 50% of high-risk patients stil
Externí odkaz:
https://doaj.org/article/dbb768f368d643d1a5a9f03a388be936
Autor:
Gaia Martire, Federica Lovisa, Elisa Carraro, Domenico Rizzato, Simone Cesaro, Rosa Maria Mura, Annalisa Tondo, Cinzia Bertolin, Francesca Boaretto, Leonardo Salviati, Alessandra Biffi, Marta Pillon, Lara Mussolin
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
Not available.
Externí odkaz:
https://doaj.org/article/cb46ad2de9d44114a2d6383d21265426
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
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100100- (2023)
Externí odkaz:
https://doaj.org/article/71e27bdd17834f0f8ad31dcf8276d12e
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100108- (2023)
Externí odkaz:
https://doaj.org/article/2feb8759d5b24c2c96ef67cf73d3868c
Publikováno v:
Biomolecules, Vol 14, Iss 2, p 159 (2024)
Since the first discovery in 1989, the β3-adrenoceptor (β3-AR) has gained great attention because it showed the ability to regulate many physiologic and metabolic activities, such as thermogenesis and lipolysis in brown and white adipose tissue, re
Externí odkaz:
https://doaj.org/article/3dd33b3b964842f3b175403a0194b30f
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