Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Valentina Ansuini"'
Autor:
Angela Mauro, Francesca Casini, Emanuele Chittano Congedo, Sara L’assainato, Francesca Pinto, Valentina Ansuini, Ruggiero Mascolo, Alice Pedroli, Luca Bernardo
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Bardet–Biedl syndrome is a rare autosomal recessive disorder characterized by rod-cone dystrophy, renal dysfunction, obesity, learning difficulties, hypogonadism, polydactyl, and many other minor features that can affect the cardiovascular, locomot
Externí odkaz:
https://doaj.org/article/e1d386a72a764ccdb95b15140d0a52a9
Autor:
Angela Mauro, Teresa Giani, Clelia Di Mari, Martina Sandini, Antonella Talenti, Valentina Ansuini, Luigi Biondi, Giovanni Di Nardo, Luca Bernardo
Publikováno v:
Children, Vol 10, Iss 2, p 309 (2023)
Systemic lupus erythematosus (SLE) is a systemic autoimmune disorder. When it presents before the age of 18 years (childhood-onset systemic lupus erythematosus, cSLE), the disease course tends to be more severe with a higher rate of organ involvement
Externí odkaz:
https://doaj.org/article/c03f86bc219a4bbfb8b146ee71e2c8fd
Autor:
Alberto Zampiero, Valentina Montinaro, Susanna Esposito, Leonardo Terranova, Valentina Ansuini, Nicola Principi, Alessia Scala
Publikováno v:
Human Vaccines & Immunotherapeutics. 9:2296-2303
Before a protein vaccine is introduced into a country, it is essential to evaluate its potential impact and estimate its benefits and costs. The aim of this study was to determine the genetic characteristics of Neisseria meningitidis B (NmB) in the p
Autor:
Lucilla Martini, Silvia Triarico, Valentina Ansuini, P. Caradonna, Valentina Paolucci, Elio Salvaggio, E. Ausili, B. Focarelli, Donato Rigante, Claudia Rendeli
Publikováno v:
Rheumatology International. 32:2737-2743
Interventions directed to the recognition of abnormal bone mineral density, bone mineral content, and body composition in the pediatric age require the definition of factors influencing bone mass acquisition during growth. We have evaluated in a cros
Autor:
Ilaria La Torraca, Gabriella De Rosa, Barbara Bertoni, Achille Stabile, Manuela Pardeo, Donato Rigante, Valentina Ansuini, Stefania Gaspari
Publikováno v:
Rheumatology International. 27:767-770
We report a case of large pericardial effusion which has been managed with pericardiocentesis as the main presentation feature of a dramatic clinical picture, only retrospectively framed as referred to macrophage activation syndrome in a child with j
Autor:
Leonardo Terranova, Nicola Principi, Valentina Ansuini, W. Peves Rios, Alessia Scala, Valentina Montinaro, Susanna Esposito, Alberto Zampiero, Carlotta Galeone
Publikováno v:
European journal of clinical microbiologyinfectious diseases : official publication of the European Society of Clinical Microbiology. 32(9)
The purpose of this investigation was to evaluate the effectiveness of posterior pharyngeal and nasopharyngeal swabs in identifying and quantifying meningococcal carriage. Two swab samples were obtained from 564 healthy adolescents aged 15–19 years
Publikováno v:
BMC Infectious Diseases, Vol 13, Iss 1, p 15 (2013)
BMC Infectious Diseases
BMC Infectious Diseases
BackgroundHemophagocytic syndrome (HPS) is clinically defined as a combination of fever, liver dysfunction, coagulation abnormalities, pancytopenia, progressive macrophage proliferation throughout the reticuloendothelial system, and cytokine over-pro
Publikováno v:
Rheumatology international. 28(8)
We report two children with autoinflammatory syndromes treated with anakinra who came in contact with the varicella-zoster virus after being exposed accidentally to infected children: both cases were managed prophylactically with specific antichicken
Autor:
Ettore Capoluongo, Adele Compagnone, Marco Piastra, Achille Stabile, Orazio Genovese, Donato Rigante, Antonio Chiaretti, Silvia Maria Modesta Pulitano, Barbara Bertoni, Valentina Ansuini
We describe for the first time a case of macrophage activation syndrome in a child with hyperimmunoglobulinemia D with periodic fever syndrome who required intensive care support. Up-regulated monokine production, high serum levels of triglycerides a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3b9dd9f44d2ea3369b757fd8ef58f8c
http://hdl.handle.net/11588/780378
http://hdl.handle.net/11588/780378
Autor:
Laura Avallone, Barbara Bertoni, Achille Stabile, Donato Rigante, Valentina Ansuini, Gilda Federico, Anna Lisa Pugliese
Publikováno v:
Rheumatology international. 27(1)
Hyperimmunoglobulinemia D/periodic fever syndrome is caused by recessively inherited mutations in the mevalonate kinase gene and is characterized by persistently high polyclonal serum IgD titre and recurrent febrile attacks. No conventional therapy e