Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Davide, Montin"'
Autor:
Ilaria Maccora, Sara Immacolata Orsini, Romina Gallizzi, Davide Montin, Marco Cattalini, Francesco La Torre, Alessandra Spagnolo, Federico Diomeda, Gabriele Simonini
Publikováno v:
Therapeutic Advances in Musculoskeletal Disease, Vol 16 (2024)
Background: Behçet disease (BD) is a rare disease in childhood and its uveitis may lead to blindness if not properly treated. Objectives: We aim to describe a cohort of paediatric BD patients with uveitis. Design: This is a multicentric retrospectiv
Externí odkaz:
https://doaj.org/article/58b96686b6374b7da11b82aa720ca6f2
Autor:
Davide Montin, Veronica Santilli, Alessandra Beni, Giorgio Costagliola, Baldassarre Martire, Maria Felicia Mastrototaro, Giorgio Ottaviano, Caterina Rizzo, Mayla Sgrulletti, Michele Miraglia Del Giudice, Viviana Moschese
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
The emergence of vaccinomics and system vaccinology represents a transformative shift in immunization strategies, advocating for personalized vaccines tailored to individual genetic and immunological profiles. Integrating insights from genomics, tran
Externí odkaz:
https://doaj.org/article/7d7a2cb1e9d14c4d807b1df0d5ae06f2
Autor:
Emilia Cirillo, Antonietta Tarallo, Elisabetta Toriello, Annamaria Carissimo, Giuliana Giardino, Antonio De Rosa, Carla Damiano, Annarosa Soresina, Raffaele Badolato, Rosa Maria Dellepiane, Lucia A. Baselli, Maria Carrabba, Giovanna Fabio, Patrizia Bertolini, Davide Montin, Francesca Conti, Roberta Romano, Elisa Pozzi, Giulio Ferrero, Roberta Roncarati, Manuela Ferracin, Alfredo Brusco, Giancarlo Parenti, Claudio Pignata
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionAtaxia telangiectasia (AT) is a rare disorder characterized by neurodegeneration, combined immunodeficiency, a predisposition to malignancies, and high clinical variability. Profiling of microRNAs (miRNAs) may offer insights into the unde
Externí odkaz:
https://doaj.org/article/fcaa1e5e99644d8590fe1280ba7fae17
Autor:
Maria Carrabba, Rosa Maria Dellepiane, Manuela Cortesi, Lucia Augusta Baselli, Annarosa Soresina, Emilia Cirillo, Giuliana Giardino, Francesca Conti, Laura Dotta, Andrea Finocchi, Caterina Cancrini, Cinzia Milito, Lucia Pacillo, Bianca Laura Cinicola, Fausto Cossu, Rita Consolini, Davide Montin, Isabella Quinti, Andrea Pession, Giovanna Fabio, Claudio Pignata, Maria Cristina Pietrogrande, Raffaele Badolato
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 19, Iss 1, Pp 1-12 (2023)
Abstract Job’s syndrome, or autosomal dominant hyperimmunoglobulin E syndrome (AD-HIES, STAT3-Dominant Negative), is a rare inborn error of immunity (IEI) with multi-organ involvement and long-life post-infective damage. Longitudinal registries are
Externí odkaz:
https://doaj.org/article/e562c8d325804325ab0a1eb01d5a36b2
Autor:
Andrea Gazzin, Francesca Pala, Marita Bosticardo, Julie Niemela, Jennifer Stoddard, Eleonora Biasin, Paola Quarello, Diana Carli, Francesca Ferroni, Ottavia M. Delmonte, Davide Montin, Sergio D. Rosenzweig, Francesco Licciardi, Luigi D. Notarangelo
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionMulibrey nanism (MUL) is a rare disorder caused by TRIM37 gene variants characterized by growth failure, dysmorphic features, congestive heart failure (CHF), and an increased risk of Wilms’ tumor. Although immune system impairment has b
Externí odkaz:
https://doaj.org/article/b64afc7eac1f4438a0e696ecab1e822e
Autor:
Joeri W. van Straalen, Sytze de Roock, Gabriella Giancane, Ekaterina Alexeeva, Elena Koskova, Pablo Mesa-del-Castillo Bermejo, Francesco Zulian, Adele Civino, Davide Montin, Nico M. Wulffraat, Nicolino Ruperto, Joost F. Swart, for the Paediatric Rheumatology International Trials Organisation (PRINTO)
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 20, Iss 1, Pp 1-10 (2022)
Abstract Background Little is known about the disposition to autoimmune diseases (ADs) among children diagnosed with JIA. In this study, we provide a comprehensive overview of the prevalence of and factors associated with ADs in parents of children w
Externí odkaz:
https://doaj.org/article/5cfb99b8852348a78d6e8d0a1455d560
Autor:
Francesco Licciardi, Carlotta Covizzi, Marta Dellepiane, Nicole Olivini, Maria Vincenza Mastrolia, Andrea Lo Vecchio, Viviana Monno, Maria Tardi, Angela Mauro, Maria Alessio, Giovanni Filocamo, Marco Cattalini, Andrea Taddio, Roberta Caorsi, Gian Luigi Marseglia, Francesco La Torre, Andrea Campana, Gabriele Simonini, Angelo Ravelli, Davide Montin
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
BackgroundThe treatment of multisystem inflammatory syndrome in children unresponsive to first-line therapies (IVIG and/or steroids) is challenging. The effectiveness of IL-1 receptor antagonist, anakinra, is debated.Patients and methodsWe conducted
Externí odkaz:
https://doaj.org/article/0ba1119c8ddc43f390653831e7309aa6
Autor:
Marco Cattalini, Sara Della Paolera, Fiammetta Zunica, Claudia Bracaglia, Manuela Giangreco, Lucio Verdoni, Antonella Meini, Rita Sottile, Roberta Caorsi, Gianvincenzo Zuccotti, Marianna Fabi, Davide Montin, Alessandra Meneghel, Alessandro Consolaro, Rosa Maria Dellepiane, Maria Cristina Maggio, Francesco La Torre, Alessandra Marchesi, Gabriele Simonini, Alberto Villani, Rolando Cimaz, Angelo Ravelli, Andrea Taddio, on behalf of the Rheumatology Study Group of the Italian Pediatric Society
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-11 (2021)
Abstract Background There is mounting evidence on the existence of a Pediatric Inflammatory Multisystem Syndrome-temporally associated to SARS-CoV-2 infection (PIMS-TS), sharing similarities with Kawasaki Disease (KD). The main outcome of the study w
Externí odkaz:
https://doaj.org/article/08f4cd297aa74509838bbfa2c4549c95
Autor:
Francesco Licciardi, Letizia Baldini, Marta Dellepiane, Carlotta Covizzi, Roberta Mogni, Giulia Pruccoli, Cecilia Orsi, Ivana Rabbone, Emilia Parodi, Federica Mignone, Davide Montin
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2022)
Externí odkaz:
https://doaj.org/article/5e2da6c3b5ae4593814bffa8ada53bff
Autor:
Francesco Licciardi, Letizia Baldini, Marta Dellepiane, Carlotta Covizzi, Roberta Mogni, Giulia Pruccoli, Cecilia Orsi, Ivana Rabbone, Emilia Parodi, Federica Mignone, Davide Montin
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Background: MIS-C is a potentially severe inflammatory syndrome associated with SARS-CoV-2 exposure. Intravenous immunoglobulin (IVIG) is considered the first-tier therapy, but it implies infusion of large fluid volumes that may worsen cardiac functi
Externí odkaz:
https://doaj.org/article/ceaf2afb2145413691b0668b601fe26d