Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Mauro, Celli"'
Autor:
Valerio Di Martino, Fabiana Mallone, Alessandro Lambiase, Mauro Celli, Alice Mannocci, Luca Celli, Pietro Mangiantini, Pasquale Fino, Antonietta Moramarco
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-8 (2024)
Abstract Purpose Blue sclera is a characteristic and common clinical sign of Osteogenesis Imperfecta (OI). However, there is currently no widely accepted, objective method for assessing and grading blue sclera in individuals with OI. To address this
Externí odkaz:
https://doaj.org/article/6d2ef98797d14cce894ed3b6d9ce848d
Autor:
Giacomo D’Angeli, Francesca Zara, Francesca Arienzo, Daniela Messineo, Mauro Celli, Gian Luca Sfasciotti, Iole Vozza, Mara Riminucci, Antonella Polimeni, Alessandro Corsi
Publikováno v:
Applied Sciences, Vol 14, Iss 22, p 10419 (2024)
Bisphophonates (BPs) are widely used in Osteogenesis imperfecta (OI). Cone Beam Computed Tomography (CBCT) shows clinical usefulness in evaluating impacted teeth and adjacent structure relationships, extraction socket healing, bone mineral density (B
Externí odkaz:
https://doaj.org/article/547fc6be32b444bdb6de83e9b481b5ad
Autor:
Luigia Cinque, Flavia Pugliese, Antonio Stefano Salcuni, Domenico Trombetta, Claudia Battista, Tommaso Biagini, Bartolomeo Augello, Grazia Nardella, Francesco Conti, Sabrina Corbetta, Rita Fischetto, Thomas Foiadelli, Agostino Gaudio, Cosimo Giannini, Enrico Grosso, Gregorio Guabello, Stefania Massuras, Andrea Palermo, Luisa Politano, Francesca Pigliaru, Rosaria Maddalena Ruggeri, Emanuela Scarano, Piera Vicchio, Salvatore Cannavò, Mauro Celli, Francesco Petrizzelli, Mario Mastroianno, Marco Castori, Alfredo Scillitani, Vito Guarnieri
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionHypophosphatasia (HPP) is a rare genetic disease caused by inactivating variants of the ALPL gene. Few data are available on the clinical presentation in Italy and/or on Italian HPP surveys.MethodsThere were 30 suspected HPP patients recr
Externí odkaz:
https://doaj.org/article/0354a004b69343bd97c812b9b831c063
Autor:
Anna Maria Comberiati, Ludovico Iannetti, Raffaele Migliorini, Marta Armentano, Marika Graziani, Luca Celli, Anna Zambrano, Mauro Celli, Magda Gharbiya, Alessandro Lambiase
Publikováno v:
Applied Sciences, Vol 13, Iss 9, p 5240 (2023)
Purpose: To evaluate ocular motility (OM) abnormalities associated with Ehlers-Danlos Syndrome (EDS). Materials and methods: In this cross-sectional observational study, patients with EDS underwent a complete orthoptic examination. The following orth
Externí odkaz:
https://doaj.org/article/f47b5aaf433d4ae684fc62d2f21fd9bc
Autor:
Maria Felicia Faienza, Albina Tummolo, Mauro Celli, Roberto Finocchiaro, Laura Piacente, Francesca Di Serio, Grazia Paola Nicchia, Giacomina Brunetti, Patrizia D’Eufemia
Publikováno v:
Biomedicines, Vol 11, Iss 2, p 458 (2023)
Brain-type creatine kinase (CK-BB) increases during osteoclastogenesis, with high circulating amounts in type I osteogenesis imperfecta (OI) following treatment with neridronate, a bisphosphonate able to inhibit osteoclast activity and survival. The
Externí odkaz:
https://doaj.org/article/fd02d20e5e604d13a6defe785450ed65
Autor:
Mauro Celli, Filippo Maria Ranaldi, Lorena Martini, Anna Zambrano, Pietro Persiani, Ciro Villani, Patrizia D'Eufemia
Publikováno v:
Journal of Pediatric Orthopaedics B. 28:179-185
Osteogenesis imperfecta (OI) is a rare congenital osteodystrophy. Patients with OI present with osteoporosis, extreme bone fragility and severe deformities of the lower limbs, which predispose them to frequent fractures. The aim of our study is to de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::324af87b7a70de713251d720155c998c
https://doi.org/10.1097/bpb.0000000000000536
https://doi.org/10.1097/bpb.0000000000000536
Autor:
Pietro Persiani, Ciro Villani, Lorena Martini, V. M. Formica, Daniele De Meo, Tommaso Speziale Varsamis, Elettra Giannini, Anna Zambrano, Valeria Calogero, Mauro Celli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::383590524006e25f3b161e634bbd5281
http://hdl.handle.net/11573/1550619
http://hdl.handle.net/11573/1550619
Autor:
Anna Maria Testi, Fiorina Giona, Alessandro Corsi, A. Turchetti, Maria Luisa Moleti, L. Celli, Miriam D'Avanzo, Anna Zambrano, Mauro Celli, Gianfranco Lapietra
Bone involvement in Hodgkin lymphoma (HL) is rare. The differential diagnosis between HL bone localization and other malignant or benign skeletal diseases is challenging. We report the case of a girl affected by classic HL, initially staged IVA becau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4464209f8033ec181d60c24e4f1e1207
http://hdl.handle.net/11573/1444586
http://hdl.handle.net/11573/1444586
Autor:
Francesca Pepe, Mauro Celli, Valeria Luzzi, Daniela Messineo, Gaetano Ierardo, Anna Zambrano, L. Celli, Antonella Polimeni, A. Turchetti
Publikováno v:
Healthcare
Volume 8
Issue 4
Healthcare, Vol 8, Iss 546, p 546 (2020)
Volume 8
Issue 4
Healthcare, Vol 8, Iss 546, p 546 (2020)
(1) Background: The aim of the work is to identify some imaging parameters in osteogenesis imperfecta to assist the dentist in the diagnosis, planning, and orthodontic treatment of Osteogenesis Imperfecta (OI) using 3D cone beam Computed Tomography (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d9900cbdbfb1a90366d4e8a95dda8f5
https://pubmed.ncbi.nlm.nih.gov/33321783
https://pubmed.ncbi.nlm.nih.gov/33321783
Autor:
Mauro Celli, Daniela Messineo, Giacomo D’Angeli, Mara Riminucci, Alessandro Corsi, Gian Luca Sfasciotti, Iole Vozza
Publikováno v:
Healthcare
Volume 8
Issue 4
Healthcare, Vol 8, Iss 372, p 372 (2020)
Volume 8
Issue 4
Healthcare, Vol 8, Iss 372, p 372 (2020)
(1) Objectives: The aim of our study was to investigate the anatomical features of lower third molar and its adjacent anatomical connections in type I Osteogenesis Imperfecta (OI) patients through cone beam computed tomography (cbct). (2) Methods: Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9cefbdb3d5ec655ba83fdb39cd904c7