Zobrazeno 1 - 10
of 341
pro vyhledávání: '"Fabrizio De Benedetti"'
Autor:
Saverio La Bella, Marina Attanasi, Annamaria Porreca, Armando Di Ludovico, Maria Cristina Maggio, Romina Gallizzi, Francesco La Torre, Donato Rigante, Francesca Soscia, Francesca Ardenti Morini, Antonella Insalaco, Marco Francesco Natale, Francesco Chiarelli, Gabriele Simonini, Fabrizio De Benedetti, Marco Gattorno, Luciana Breda
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-11 (2024)
Abstract Background Artificial intelligence (AI) has become a popular tool for clinical and research use in the medical field. The aim of this study was to evaluate the accuracy and reliability of a generative AI tool on pediatric familial Mediterran
Externí odkaz:
https://doaj.org/article/dd5991ca2dfc471386a38e30914e8cd4
Autor:
Rashmi Sinha, Fabrizio De Benedetti, Alexei A. Grom, on behalf of the participants listed below
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss S1, Pp 1-4 (2024)
Externí odkaz:
https://doaj.org/article/f6fcee9e7a5743ddb56279b2265e501a
Autor:
Peter A. Nigrovic, Fabrizio de Benedetti, Yukiko Kimura, Daniel J. Lovell, Sebastiaan J. Vastert
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss S1, Pp 1-7 (2024)
Abstract Currently, the criteria used to classify patients with SJIA are different from those used for AOSD. However, it has been recognized that the existing terms are too narrow, subdividing the Still’s population unnecessarily between pediatric-
Externí odkaz:
https://doaj.org/article/6678de9be18f407a88a36fab07a84e7a
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss S1, Pp 1-4 (2024)
Abstract The substantial morbidity and mortality associated with refractory systemic JIA underlies the need for new treatment approaches. However, progress in this area has been limited by the difficulty of enrolling these patients in clinical trials
Externí odkaz:
https://doaj.org/article/a701bfd93a34490baa23aa947625826b
Autor:
Scott W. Canna, Fabrizio De Benedetti
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 21, Iss S1, Pp 1-6 (2024)
Abstract Since IL-18 has recently emerged as a biomarker associated with refractory disease course in SJIA, the focus of the discussion was the feasibility of the biomarker-driven drug development to SJIA. Overall, there was broad agreement on the co
Externí odkaz:
https://doaj.org/article/537d6e32416e48f980b48ea3ec208ea9
Autor:
Patricia Morán-Álvarez, Alessandra Gianviti, Francesca Diomedi-Camassei, Monia Ginevrino, Fabrizio de Benedetti, Claudia Bracaglia
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 22, Iss 1, Pp 1-5 (2024)
Abstract Background Childhood systemic lupus erythematosus (cSLE) has been considered as a polygenic autoimmune disease; however, a monogenic lupus-like phenotype is emerging with the recent recognition of several related novel high-penetrance geneti
Externí odkaz:
https://doaj.org/article/acfce8b70faa432595efb08e28dad688
Autor:
Marianna Nicoletta Rossi, Valentina Matteo, Francesca Diomedi-Camassei, Ester De Leo, Olivier Devuyst, Mohamed Lamkanfi, Ivan Caiello, Elena Loricchio, Francesco Bellomo, Anna Taranta, Francesco Emma, Fabrizio De Benedetti, Giusi Prencipe
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Cystinosis is a rare autosomal recessive disorder caused by mutations in the CTNS gene that encodes cystinosin, a ubiquitous lysosomal cystine/H+ antiporter. The hallmark of the disease is progressive accumulation of cystine and cystine crystals in v
Externí odkaz:
https://doaj.org/article/a1638def141045a1a1850f75b41d76d3
Autor:
Laura De Nardi, Marco Francesco Natale, Virginia Messia, Paolo Tomà, Fabrizio De Benedetti, Antonella Insalaco
Publikováno v:
Italian Journal of Pediatrics, Vol 49, Iss 1, Pp 1-5 (2023)
Abstract Background Ataxia-telangiectasia (A-T) is a rare autosomal recessive DNA repair disorder, characterized by progressive cerebellar degeneration, telangiectasia, immunodeficiency, recurrent sinopulmonary infections, radiation sensitivity, prem
Externí odkaz:
https://doaj.org/article/b29d5f586ddb4dfaafa39c065a09a55c
Autor:
Fabrizio Leone, Nicola Cotugno, Chiara Casamento Tumeo, Paola Zangari, Patrizia Palomba, Rachele Adorisio, Fabrizio De Benedetti, Claudia Bracaglia, Paola Papoff, Camilla Ajassa, Paolo Palma, Stefania Bernardi
Publikováno v:
BMC Infectious Diseases, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Introduction Haemophagocytic lymphohistiocytosis is a rare and life-threatening condition caused by uncontrolled immune activation leading to excessive inflammation and tissue destruction. It could either be due to a primary genetic defect o
Externí odkaz:
https://doaj.org/article/bf1b0d057edb4a3a884c6af4980a3002
Autor:
Franco Locatelli, Claudia Bracaglia, Pietro Merli, Mattia Algeri, Rebecca Nicolai, Fabrizio de Benedetti, Emiliano Marasco, Patricia Moran Alvarez, Maria Giuseppina Cefalo, Marco Becilli
Publikováno v:
Lupus Science and Medicine, Vol 11, Iss Suppl 1 (2024)
Externí odkaz:
https://doaj.org/article/a0731b78b8a64e8e92bd9011b483df8e