Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Camilla Caldarini"'
Autor:
Camilla Caldarini, Francesco Andrea Causio, Marco Castori, Matteo Cassina, Vito Guarnieri, Carmela Fusco, Tommaso Biagini, Massimiliano Copetti, Alessandro De Luca, Simona Petrucci, Bartolomeo Augello, Antonio Petracca, Annalisa Rella, Lucia Micale, Leonardo D'Agruma, Rita Fischetto, Maria Cecilia D'Asdia, F. Annunziata, Grazia Nardella, Francesco Brancati, Teresa Mattina, Mario Bengala
Publikováno v:
Human Molecular Genetics. 28:2133-2142
Hereditary multiple osteochondromas (HMO) is a rare autosomal dominant skeletal disorder, caused by heterozygous variants in either EXT1 or EXT2, which encode proteins involved in the biogenesis of heparan sulphate. Pathogenesis and genotype-phenotyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e110582f4f17ca201d9af29d194f73c
https://doi.org/10.1093/hmg/ddz046
https://doi.org/10.1093/hmg/ddz046
Autor:
Paolo Trezza, Lucrezia Montanari, Antonio Memeo, Daniele Priano, Camilla Caldarini, Melania Laquidara, Pietro Randelli
Publikováno v:
Minerva pediatrica.
Background The study aim is to share our experience in hospital re-organization and management of paediatric traumatology in the early stage of COVID-19 pandemic. We centralized paediatric traumatology supposing a reduction of ER admissions, with inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19ba38088d77e0d4f98cd674084d6380
https://pubmed.ncbi.nlm.nih.gov/33016683
https://pubmed.ncbi.nlm.nih.gov/33016683
Objective The purpose of this clinical case-control study was to assess the level of sports activity in children with hereditary multiple exostoses (HME) and to compare with the degree of physical activity in children of the same age without patholog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99106b99982cc0a374070fa0f697ce70
https://hdl.handle.net/2434/946859
https://hdl.handle.net/2434/946859
Autor:
Nicola Serra, Camilla Caldarini, Vincenza Ragone, Federico Giuseppe Usuelli, Riccardo D’Ambrosi, Renato Mario Facchini
The aim of the study was to evaluate quality of life (QOL), global health status, pain, and level of satisfaction in patients with hereditary multiple exostoses (HME), and to correlate the association between the severity of diseases and age, sex, nu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7a7488bc0d7429c87abb6d5ceb4bb64
https://hdl.handle.net/2434/946885
https://hdl.handle.net/2434/946885
Autor:
Massimiliano Chetta, Pietro Palumbo, Paola Raiteri, Filomena Baorda, Camilla Caldarini, Michele Ciavarella, Renato Mario Facchini, Margherita Silengo, Leonardo D'Agruma, Luigi Bisceglia, Mario Bengala, Vito Guarnieri, Maria Luigia Cavaliere, Roberto Lala, Pietro Stanziale, Barbara Pasini, Michelina Coco, Leopoldo Zelante, Davide De Brasi
Background Hereditary multiple exostosis represents the most frequent bone tumor disease in humans. It consists of cartilage deformities affecting the juxta-ephyseal region of long bones. Usually benign, exostosis could degenerate in malignant chondr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58cd28ae94843bbb012ff5c2992dec23
http://hdl.handle.net/2318/128680
http://hdl.handle.net/2318/128680
Autor:
Renato Mario Facchini, Camilla Caldarini, Riccardo D’Ambrosi, Elena Biancardi, Alessia Barbato
Publikováno v:
Journal of Children's Orthopaedics
Purpose Deformities of the forearm and shortening of the ulna occur in 30 % of patients with hereditary multiple exostoses (HME), leading to radial head dislocation and loss of movement. Several surgical techniques have been described for treatment,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d1fd03afc77e242533e623ecd3b1696