Zobrazeno 1 - 10
of 5 109
pro vyhledávání: '"Pession A."'
Autor:
Roberto Rondelli, Tamara Belotti, Riccardo Masetti, Franco Locatelli, Maura Massimino, Alessandra Biffi, Carlo Dufour, Franca Fagioli, Giuseppe Menna, Andrea Biondi, Claudio Favre, Marco Zecca, Nicola Santoro, Giovanna Russo, Silverio Perrotta, Andrea Pession, Arcangelo Prete
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-9 (2024)
Abstract Background In Italy, there is a network of centres headed by the Italian Association of Pediatric Hematology and Oncology (AIEOP) for the diagnosis and treatment of paediatric cancers on almost the entire national territory. Nevertheless, mi
Externí odkaz:
https://doaj.org/article/187b8f29096d4a3dad2c8ddcafe11c1e
Autor:
Bond, Simon, Bordugo, Andrea, Brodosi, Lucia, Camilot, Marta, Carubbi, Francesca, Dardis, Andrea, Dianin, Alice, Vici, Carlo Dionisi, Donati, Maria Alice, Fasan, Ilaria, Federico, Antonio, Filosto, Massimiliano, Gasperini, Serena, La Marca, Giancarlo, Martinelli, Diego, Noto, Davide, Spada, Marco, Toscano, Antonio, Vitturi, Nicola, Sechi, Annalisa, Urban, Maria Letizia, Murphy, Elaine, Pession, Andrea, Scarpa, Maurizio
Publikováno v:
In Nutrition, Metabolism and Cardiovascular Diseases November 2024 34(11):2440-2445
Publikováno v:
Biomolecules, Vol 14, Iss 10, p 1249 (2024)
Bacterial Lysates are immunostimulants clinically prescribed for the prevention of respiratory tract infections (RTIs). It has been shown that Bacterial Lysates upregulate the immune system, acting both on innate and adaptive reactions. In fact, ther
Externí odkaz:
https://doaj.org/article/226ad988bb784f52a20ad115d95e20f9
Autor:
Giuseppe Maglietta, Matteo Puntoni, Caterina Caminiti, Andrea Pession, Marcello Lanari, Fabio Caramelli, Federico Marchetti, Alessandro De Fanti, Lorenzo Iughetti, Giacomo Biasucci, Agnese Suppiej, Andrea Miceli, Chiara Ghizzi, Gianluca Vergine, Melodie Aricò, Marcello Stella, Susanna Esposito, Emilia-Romagna Paediatric COVID-19 network, Francesca Diodati, Chiara Maria Palo, Angela Miniaci, Luca Bertelli, Giovanni Biserni, Angela Troisi, Alessandra Iacono, Federico Bonvicini, Domenico Bartolomeo, Andrea Trombetta, Tommaso Zini, Nicoletta de Paulis, Cristina Forest, Battista Guidi, Francesca Di Florio, Enrico Valletta, Francesco Accomando, Greta Ramundo, Alberto Argentiero, Valentina Fainardi, Michela Deolmi
Publikováno v:
Frontiers in Public Health, Vol 12 (2024)
BackgroundThe use of Non-Pharmaceutical Interventions (NPIs), such as lockdowns, social distancing and school closures, against the COVID-19 epidemic is debated, particularly for the possible negative effects on vulnerable populations, including chil
Externí odkaz:
https://doaj.org/article/5c8e1238a97c42218331549f154cc6b2
Autor:
Daniele Zama, Egidio Candela, Gennaro Pagano, Francesco Venturelli, Fraia Melchionda, Francesco Toni, Mino Zucchelli, Andrea Pession
Publikováno v:
Clinical Case Reports, Vol 12, Iss 3, Pp n/a-n/a (2024)
Key Clinical Message Spinal cord compression from non‐Hodgkin lymphoma (NHL) should be considered as a potential diagnosis in cases of acute signs of myelopathy in pediatric patients. Abstract Spinal cord compression in pediatric non‐Hodgkin lymp
Externí odkaz:
https://doaj.org/article/4e28b08bc5af4a2fbfeeb5196848af68
Autor:
Lucia Brodosi, Michele Stecchi, Dorina Mita, Francesca Marchignoli, Valeria Guarneri, Giulio Agnelli, Valentino Osti, Federica Perazza, Federica Sacilotto, Andrea Pession, Loris Pironi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-7 (2023)
Abstract Background The Covid pandemic seems to have had several detrimental effects on managing patients affected by inherited metabolic diseases (IMD), although published data about the impact of COVID-19 on patients suffering from IMD are very sca
Externí odkaz:
https://doaj.org/article/2af369cd51594312a7107c85d05cf9bf
Autor:
Daria Messelodi, Silvia Strocchi, Salvatore Nicola Bertuccio, Pascale Baden, Valentina Indio, Federico M. Giorgi, Alberto Taddia, Salvatore Serravalle, Sabrina Valente, Alessio di Fonzo, Emanuele Frattini, Roberto Bernardoni, Annalisa Pession, Daniela Grifoni, Michela Deleidi, Annalisa Astolfi, Andrea Pession
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-13 (2023)
Abstract Gaucher Disease (GD), the most common lysosomal disorder, arises from mutations in the GBA1 gene and is characterized by a wide spectrum of phenotypes, ranging from mild hematological and visceral involvement to severe neurological disease.
Externí odkaz:
https://doaj.org/article/9bd17c548d7444108e9aef7cad700e02
Autor:
Maja Di Rocco, Carlo Dionisi Vici, Alberto Burlina, Francesco Venturelli, Agata Fiumara, Simona Fecarotta, Maria Alice Donati, Marco Spada, Daniela Concolino, Andrea Pession
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-6 (2023)
Abstract Background GD and ASMD are lysosomal storage disorders that enter into differential diagnosis due to the possible overlap in their clinical manifestations. The availability of safe and effective enzymatic therapies has recently led many inve
Externí odkaz:
https://doaj.org/article/8945f64473ae4b1884493f16f820f68a
Autor:
Andrea Pession, Maja Di Rocco, Francesco Venturelli, Barbara Tappino, William Morello, Nicola Santoro, Paola Giordano, Beatrice Filippini, Simona Rinieri, Giovanna Russo, Katia Girardi, Antonio Ruggiero, Eulalia Galea, Roberto Antonucci, Nicola Tovaglieri, Fulvio Porta, Immacolata Tartaglione, Fiorina Giona, Franca Fagioli, Alberto Burlina, Pediatric Gaucher Study Group
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background Gaucher disease (GD) diagnosis can be delayed due to non-specific symptoms and lack of awareness, leading to unnecessary procedures and irreversible complications. GAU-PED study aims to assess GD prevalence in a high-risk pediatri
Externí odkaz:
https://doaj.org/article/92faecc5e2424f989cb71afd6db08634
Autor:
Carlotta Spagnoli, Roberta Battini, Filippo Manti, Duccio Maria Cordelli, Andrea Pession, Melissa Bellini, Andrea Bordugo, Gaetano Cantalupo, Antonella Riva, Pasquale Striano, Marco Spada, Francesco Porta, Carlo Fusco
Publikováno v:
Behavioural Neurology, Vol 2024 (2024)
Introduction. AADCd is an ultrarare, underdiagnosed neurometabolic disorder for which a screening test (3-OMD dosing on dried blood spot (DBS)) and targeted gene therapy (authorized in the EU and the UK) are available. Therefore, it is mandatory to r
Externí odkaz:
https://doaj.org/article/14bb14f2996c4f5da9b495ff7750dc88