Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Emma C. Manno"'
Autor:
Gabriella Bottari, Valerio Confalone, Nicola Cotugno, Isabella Guzzo, Salvatore Perdichizzi, Emma C. Manno, Francesca Stoppa, Corrado Cecchetti
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: Multisystem inflammatory syndrome in children (MIS-C) has emerged during the COVID-19 pandemic as a new SARS-CoV-2-related entity, potentially responsible for a life-threatening clinical condition associated with myocardial dysfunction an
Externí odkaz:
https://doaj.org/article/083596b853f34443ace057fcd36607f1
Autor:
Paolo Palma, Lindvi Gudmundsdotter, Andrea Finocchi, Lars E. Eriksson, Nadia Mora, Veronica Santilli, Angela Aquilani, Emma C. Manno, Paola Zangari, Maria Luisa Romiti, Carla Montesano, Alba Grifoni, Andreas Brave, Karl Ljungberg, Pontus Blomberg, Stefania Bernardi, Eric Sandström, Bo Hejdeman, Paolo Rossi, Britta Wahren
Publikováno v:
Vaccines, Vol 2, Iss 3, Pp 563-580 (2014)
Therapeutic HIV immunization is intended to induce new HIV-specific cellular immune responses and to reduce viral load, possibly permitting extended periods without antiretroviral drugs. A multigene, multi-subtype A, B, C HIV-DNA vaccine (HIVIS) has
Externí odkaz:
https://doaj.org/article/554178c31a8b407ab0f3d8b96805240a
Autor:
Sonia Zicari, Libera Sessa, Nicola Cotugno, Alessandra Ruggiero, Elena Morrocchi, Carlo Concato, Salvatore Rocca, Paola Zangari, Emma C. Manno, Paolo Palma
Publikováno v:
Viruses, Vol 11, Iss 3, p 200 (2019)
Despite effective antiretroviral therapy (ART), people living with HIV (PLWH) still present persistent chronic immune activation and inflammation. This condition is the result of several factors including thymic dysfunction, persistent antigen stimul
Externí odkaz:
https://doaj.org/article/282affdc43ec498289c7e00978b0442b
Autor:
Paola Ariganello, Giulia Angelino, Alessia Scarselli, Irene Salfa, Martina Della Corte, Arianna De Matteis, Patrizia D'Argenio, Susanna Livadiotti, Emma C. Manno, Cristina Russo, Andrea Finocchi, Caterina Cancrini
Publikováno v:
Case Reports in Pediatrics, Vol 2013 (2013)
X-linked agammaglobulinemia (XLA) is a primary immunodeficiency of the humoral compartment, due to a mutation in the Bruton tyrosine kinase (BTK) gene, characterized by a severe defect of circulating B cells and serum immunoglobulins. Recurrent infec
Externí odkaz:
https://doaj.org/article/68813fd36ca1419694b8b780abd3585a