Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Cristina Cifaldi"'
Autor:
Mayla Sgrulletti, Lucia Augusta Baselli, Riccardo Castagnoli, Elisabetta Del Duca, Simona Graziani, Giusella Maria Francesca Moscato, Silvia Di Cesare, Gigliola Di Matteo, Cristina Cifaldi, Martina Rossano, Claudia Ballerini, Alfonso Piciocchi, Amelia Licari, Gian Luigi Marseglia, Rita Consolini, Viviana Moschese
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 15, p 4321 (2024)
Background: An unclassified primary antibody deficiency (unPAD) is a widely heterogeneous clinical entity, recently identified within the spectrum of Inborn Errors of Immunity (IEIs). Since unPAD has been traditionally considered as a mild condition,
Externí odkaz:
https://doaj.org/article/04af5aaa56b94b94ab173bc5aca41b1f
Autor:
Enrico Attardi, Beatrice Rivalta, Cristina Cifaldi, Vittorio Rosti, Lucia Pacillo, Hajro Hajrullaj, Silvia Di Cesare, Matteo Luciani, Federica Barzaghi, Andrea Finocchi, Gigliola Di Matteo, Alessandro Aiuti, Franco Locatelli, Maria Teresa Voso, Giuseppe Palumbo, Caterina Cancrini
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100104- (2023)
Externí odkaz:
https://doaj.org/article/57160d0188904592ab83cfb84e7cc33d
Autor:
Mayla Sgrulletti, Cristina Cifaldi, Silvia Di Cesare, Barbara Kroegler, Elisabetta Del Duca, Valentina Ferradini, Simona Graziani, Mario Bengala, Gigliola Di Matteo, Viviana Moschese
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2023)
Over the last decades, Inborn Errors of Immunity (IEI) characterized by an immune dysregulatory picture, isolated or combined with infections, have been increasingly identified and referred as Primary Immune Regulatory Disorders (PIRD). PIRD diagnosi
Externí odkaz:
https://doaj.org/article/40ecff1dcbd4493b9da2b7d397ebddfb
Autor:
Lucia Pacillo, Giuliana Giardino, Donato Amodio, Carmela Giancotta, Beatrice Rivalta, Gioacchino Andrea Rotulo, Emma Concetta Manno, Cristina Cifaldi, Giuseppe Palumbo, Claudio Pignata, Paolo Palma, Paolo Rossi, Andrea Finocchi, Caterina Cancrini
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Primary Immunodeficiencies (PID) are a group of rare congenital disorders of the immune system. Autoimmune cytopenia (AIC) represents the most common autoimmune manifestation in PID patients. Treatment of AIC in PID patients can be really challenging
Externí odkaz:
https://doaj.org/article/ff47c9012e424b798480cbddb56fab44
Autor:
Biagio Di Lorenzo, Lucia Pacillo, Giulia Milardi, Tatiana Jofra, Silvia Di Cesare, Jolanda Gerosa, Ilaria Marzinotto, Ettore Zapparoli, Beatrice Rivalta, Cristina Cifaldi, Federica Barzaghi, Carmela Giancotta, Paola Zangari, Novella Rapini, Annalisa Deodati, Giada Amodio, Laura Passerini, Paola Carrera, Silvia Gregori, Paolo Palma, Andrea Finocchi, Vito Lampasona, Maria Pia Cicalese, Riccardo Schiaffini, Gigliola Di Matteo, Ivan Merelli, Matteo Barcella, Alessandro Aiuti, Lorenzo Piemonti, Caterina Cancrini, Georgia Fousteri
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
The immunological events leading to type 1 diabetes (T1D) are complex and heterogeneous, underscoring the necessity to study rare cases to improve our understanding. Here, we report the case of a 16-year-old patient who showed glycosuria during a reg
Externí odkaz:
https://doaj.org/article/2b1b1cf05e7a4bc8b5778f5273847b41
Autor:
Maria Chiriaco, Giorgiana Madalina Ursu, Donato Amodio, Nicola Cotugno, Stefano Volpi, Francesco Berardinelli, Simone Pizzi, Cristina Cifaldi, Matteo Zoccolillo, Ignazia Prigione, Silvia Di Cesare, Carmela Giancotta, Elisa Anastasio, Beatrice Rivalta, Lucia Pacillo, Paola Zangari, Alessandro G. Fiocchi, Andrea Diociaiuti, Alessandro Bruselles, Francesca Pantaleoni, Andrea Ciolfi, Valentina D’Oria, Giuseppe Palumbo, Marco Gattorno, Maya El Hachem, Jean-Pierre de Villartay, Andrea Finocchi, Paolo Palma, Paolo Rossi, Marco Tartaglia, Alessandro Aiuti, Antonio Antoccia, Gigliola Di Matteo, Caterina Cancrini
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Actin-related protein 2/3 complex subunit 1B (ARPC1B) deficiency is a recently described inborn error of immunity (IEI) presenting with combined immunodeficiency and characterized by recurrent infections and thrombocytopenia. Manifestations of immune
Externí odkaz:
https://doaj.org/article/89e21088048d4dbf915918df0ba93f6a
Autor:
Donato Amodio, Alessandra Ruggiero, Mayla Sgrulletti, Chiara Pighi, Nicola Cotugno, Chiara Medri, Elena Morrocchi, Luna Colagrossi, Cristina Russo, Salvatore Zaffina, Gigliola Di Matteo, Cristina Cifaldi, Silvia Di Cesare, Beatrice Rivalta, Lucia Pacillo, Veronica Santilli, Carmela Giancotta, Emma Concetta Manno, Marta Ciofi Degli Atti, Massimiliano Raponi, Paolo Rossi, Andrea Finocchi, Caterina Cancrini, Carlo Federico Perno, Viviana Moschese, Paolo Palma
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Mass SARS-Cov-2 vaccination campaign represents the only strategy to defeat the global pandemic we are facing. Immunocompromised patients represent a vulnerable population at high risk of developing severe COVID-19 and thus should be prioritized in t
Externí odkaz:
https://doaj.org/article/9229bbff551247e3b32221fa6dc23567
Autor:
Francesca Conti, Arianna Catelli, Cristina Cifaldi, Lucia Leonardi, Rita Mulè, Marco Fusconi, Vittorio Stefoni, Maria Chiriaco, Beatrice Rivalta, Silvia Di Cesare, Gioacchino Schifino, Fabiana Sbrega, Gigliola Di Matteo, Simona Ferrari, Caterina Cancrini, Andrea Pession
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Externí odkaz:
https://doaj.org/article/340d1111d93d4dfcb55ffecf6793a741
Autor:
Beatrice Rivalta, Donato Amodio, Cinzia Milito, Maria Chiriaco, Silvia Di Cesare, Carmela Giancotta, Francesca Conti, Veronica Santilli, Lucia Pacillo, Cristina Cifaldi, Maria Giovanna Desimio, Margherita Doria, Isabella Quinti, Rita De Vito, Gigliola Di Matteo, Andrea Finocchi, Paolo Palma, Antonino Trizzino, Alberto Tommasini, Caterina Cancrini
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Activated PI3K-kinase Delta Syndrome (APDS) is an autosomal-dominant primary immunodeficiency (PID) caused by the constitutive activation of the PI3Kδ kinase. The consequent hyperactivation of the PI3K-Akt-mTOR pathway leads to an impaired T- and B-
Externí odkaz:
https://doaj.org/article/073f1183b72c4cb19b40037c3df35304
Autor:
Francesca Conti, Arianna Catelli, Cristina Cifaldi, Lucia Leonardi, Rita Mulè, Marco Fusconi, Vittorio Stefoni, Maria Chiriaco, Beatrice Rivalta, Silvia Di Cesare, Gioacchino Schifino, Fabiana Sbrega, Gigliola Di Matteo, Simona Ferrari, Caterina Cancrini, Andrea Pession
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Introduction: Activated phosphoinositide 3-kinase-δ syndrome 2 (APDS2) is a rare primary immune regulatory disorder caused by heterozygous gain of function mutation in the PIK3R1 gene encoding PI3Kδ regulatory p85α subunit and resulting in PI3Kδ
Externí odkaz:
https://doaj.org/article/202e3e71a2374b7cbf1e6bc4be7dd90e