Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Marco Burrone"'
Autor:
Marco Burrone, Marta Mazzoni, Roberta Naddei, Angela Pistorio, Maddalena Spelta, Silvia Scala, Elisa Patrone, Marco Garrone, Maria Lombardi, Luca Villa, Giulia Pascale, Roberto Cavanna, Nicolino Ruperto, Angelo Ravelli, Alessandro Consolaro, for the Paediatric Rheumatology International Trials Organisation (PRINTO)
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 20, Iss 1, Pp 1-10 (2022)
Abstract Background Although a satisfactory disease control is nowadays achievable in most patients with JIA, a substantial proportion of them still do not respond adequately or reach long-term drug-free remission. According to current recommendation
Externí odkaz:
https://doaj.org/article/e954dcb5b07b4fd299de524964b43ca2
Autor:
Nicolino Ruperto, Ekaterina Alexeeva, Tamàs Constantin, Ivan Foeldvari, Angelo Ravelli, Gerd Horneff, Gaëlle Chédeville, Giovanni Filocamo, Alessandro Consolaro, Marco Burrone, Gabriella Giancane, Alessandra Alongi, Roberta Naddei, Valentina Natoli, Francesca Ridella, Silvia Rosina
Publikováno v:
RMD Open, Vol 8, Iss 1 (2022)
Externí odkaz:
https://doaj.org/article/f38a2f8df82944d4868c0c8b45756e2a
Autor:
Roberta Naddei, Ana Rebollo-Giménez, Marco Burrone, Valentina Natoli, Silvia Rosina, Alessandro Consolaro, Angelo Ravelli
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 1, p 367 (2023)
Juvenile psoriatic arthritis (JPsA) accounts for 1–7% of all cases of juvenile idiopathic arthritis (JIA) and its definition has been a matter of controversy among pediatric rheumatologists for many years. The traditional attribution of JPsA to the
Externí odkaz:
https://doaj.org/article/bfbc6039e924456ab73b920de7ccb02e
Autor:
Chiara Mameli, Giulia Zichichi, Nasim Mahmood, Siham Chafai Elalaoui, Adnan Mirza, Poonam Dharmaraj, Marco Burrone, Elisa Cattaneo, Jayesh Sheth, Ajit Gandhi, Gurpreet Singh Kochar, Fowzan Sami Alkuraya, Madhulika Kabra, Giuseppe Mercurio, Gianvincenzo Zuccotti
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Raine syndrome (RS) is a rare autosomal recessive disorder caused by biallelic loss-of-function mutations of FAM20C. The most common clinical features are microcephaly, exophthalmos, hypoplastic nose and severe midface hypoplasia,
Externí odkaz:
https://doaj.org/article/31e8b21d16564a75b2b20ef07336fb0c
Autor:
Roberta Naddei, Ana Rebollo-Giménez, Marco Burrone, Valentina Natoli, Silvia Rosina, Alessandro Consolaro, Angelo Ravelli
Publikováno v:
Journal of clinical medicine. 12(1)
Juvenile psoriatic arthritis (JPsA) accounts for 1–7% of all cases of juvenile idiopathic arthritis (JIA) and its definition has been a matter of controversy among pediatric rheumatologists for many years. The traditional attribution of JPsA to the
Autor:
Alessandra Alongi, Gabriella Giancane, Roberta Naddei, Valentina Natoli, Francesca Ridella, Marco Burrone, Silvia Rosina, Gaelle Chedeville, Ekaterina Alexeeva, Gerd Horneff, Ivan Foeldvari, Giovanni Filocamo, Tamàs Constantin, Nicolino Ruperto, Angelo Ravelli, Alessandro Consolaro
Publikováno v:
RMD open. 8(1)
ObjectiveTo investigate the frequency in which the physician provides a global assessment of disease activity (PhGA) >0 and an active joint count (AJC)=0 in children with juvenile idiopathic arthritis (JIA) and search for determinants of divergence b
Publikováno v:
International Journal of Pediatrics and Child Health. 8:30-32
Objective; Nervous system dysfunction, including irritability, emotional lability and hyperkinesia are the signs and symptoms frequently observed in hyperthyroidism; chorea and/or choreoathetosis have also been reported in adults and rarely in pediat
Autor:
Fowzan S. Alkuraya, Elisa Cattaneo, Jayesh Sheth, Giulia Zichichi, Madhulika Kabra, Chiara Mameli, Gurpreet Singh Kochar, Gian Vincenzo Zuccotti, Poonam Dharmaraj, Nasim Mahmood, Marco Burrone, Giuseppe Mercurio, Siham Chafai Elalaoui, Ajit Gandhi, Adnan Mirza
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Raine syndrome (RS) is a rare autosomal recessive disorder caused by biallelic loss-of-function mutations of FAM20C. The most common clinical features are microcephaly, exophthalmos, hypoplastic nose and severe midface hypoplasia, leading
Autor:
S. Agazzi, C. Vattiato, Costanza Alvisi, Catherine Klersy, Ombretta Luinetti, Gregorio Maiorano, Marco Burrone, Gino Roberto Corazza, Federico Biagi, Annalisa Schiepatti
Publikováno v:
Journal of Clinical Pathology. 69:1051-1054
Aims The utility of the 7 level Marsh–Oberhuber classification of mucosal damage in patients with coeliac disease has recently been criticised. Analysis of duodenal biopsies with dissecting microscopy is an unsophisticated method that, however, pro