Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Mario Pagnoni"'
Autor:
Andrea Cassoni, Valentina Terenzi, Davina Bartoli, Oriana Rajabtork Zadeh, Andrea Battisti, Mario Pagnoni, Davide Conte, Alessandro Lembo, Sandro Bosco, Francesco Alesini, Valentino Valentini
Publikováno v:
Case Reports in Oncological Medicine, Vol 2014 (2014)
Uterine leiomyosarcoma (LMS) is a rare tumor constituting 1% of all uterine malignancies. This sarcoma demonstrates an aggressive growth pattern with an high rate of recurrence with hematologic dissemination; the most common sites are lung, liver, an
Externí odkaz:
https://doaj.org/article/bdeaaf0d04d145f48d12439e17ff8136
Publikováno v:
Bio-Design and Manufacturing. 6:82-89
Publikováno v:
Advances on Mechanics, Design Engineering and Manufacturing IV ISBN: 9783031159275
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c645f0cb5f66657ed81b6df4fecbbd7
https://doi.org/10.1007/978-3-031-15928-2_20
https://doi.org/10.1007/978-3-031-15928-2_20
Autor:
Maria Teresa Fadda, Sebastiano Bianca, Dario Cocciadiferro, Bruno Dallapiccola, Marina Goldoni, Maria Grazia Giuffrida, Bruno Marino, Silvana Briuglia, Marco Tartaglia, Leila B. Salehi, Valentina Guida, Francesca Forzano, Orazio Palumbo, Francesco Benedicenti, Francesco Pancheri, Franco Stanzial, Laura Bernardini, Daniela Melis, Marco Castori, Giorgio Iannetti, Teresa Mattina, Marianna Puzzo, Hossein Hozhabri, Chiara Barone, Massimo Carella, Carolina Putotto, Alessandro De Luca, Francesca Piceci Sparascio, Maria Cristina Digilio, Francesco Brancati, Mario Pagnoni, Ariana Kariminejad
Publikováno v:
Clinical Genetics. 100:268-279
Oculo-auriculo-vertebral spectrum (OAVS) is a developmental disorder of craniofacial morphogenesis. Its etiology is unclear, but assumed to be complex and heterogeneous, with contribution of both genetic and environmental factors. We assessed the occ
Autor:
Agnese Brunzini, Manila Caragiuli, Marco Mandolini, Alida Mazzoli, Mario Pagnoni, Michele Germani
Publikováno v:
Lecture Notes in Mechanical Engineering ISBN: 9783030912338
Lecture Notes in Mechanical Engineering
Lecture Notes in Mechanical Engineering
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fb133378c7f3797f1ae36bec5ca4345
https://doi.org/10.1007/978-3-030-91234-5_13
https://doi.org/10.1007/978-3-030-91234-5_13
Autor:
Eleonora Brandoni Serrani, Alida Mazzoli, Agnese Brunzini, Michele Germani, Mario Pagnoni, Marco Mandolini
Publikováno v:
Proceedings of the Design Society: International Conference on Engineering Design. 1:709-718
This study defines a methodological procedure for the design and manufacturing of a prosthetic implant for the reconstruction of a midsagittal bony-deficiency of the skull due to the Apert congenital disorder. Conventional techniques for craniofacial
Autor:
Marco Mandolini, Mario Pagnoni, Steve Manieri, Michele Germani, Agnese Brunzini, Alida Mazzoli
Publikováno v:
Rapid Prototyping Journal. 25:95-103
PurposeOrbital fractures are the most commonly encountered midfacial fractures, and usually, the fracture involves the floor and/or the medial wall of the orbit. This paper aims to present an innovative approach for primary and secondary reconstructi
Autor:
Leila Bagherjad Salehi, Giorgio Iannetti, Sebastiano Bianca, Tommaso Mazza, Valentina Guida, Daniela Melis, Silvana Briuglia, Bruno Dallapiccola, Romano Tenconi, Alessandro De Luca, Francesca Piceci-Sparascio, Luigi Corsaro, Maria Teresa Fadda, Davide Gentilini, Francesca Forzano, Teresa Mattina, Enza Maria Valente, Paolo Prontera, Maria Cristina Digilio, Mario Pagnoni, Francesco Brancati, Luciano Calzari, Laura Bernardini
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 3
International Journal of Molecular Sciences, Vol 22, Iss 1190, p 1190 (2021)
Volume 22
Issue 3
International Journal of Molecular Sciences, Vol 22, Iss 1190, p 1190 (2021)
Oculo-auriculo-vertebral-spectrum (OAVS
OMIM 164210) is a rare disorder originating from abnormal development of the first and second branchial arch. The clinical phenotype is extremely heterogeneous with ear anomalies, hemifacial microsomia, oc
OMIM 164210) is a rare disorder originating from abnormal development of the first and second branchial arch. The clinical phenotype is extremely heterogeneous with ear anomalies, hemifacial microsomia, oc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ac3b407c003c585cfcff505f4708fe8
http://hdl.handle.net/11697/158419
http://hdl.handle.net/11697/158419
Autor:
Sri Gore, Gabriela Grimaldi, Giacomilde Mazzone, Richard Collin, Gustavo Savino, Mario Pagnoni, Alessandra Modugno
Publikováno v:
The British journal of ophthalmology.
Background/AimsMicrophthalmia and anophthalmia are rare conditions, which represent ocular maldevelopment; both may be associated with orbital cysts. Current literature recommends retention to stimulate orbital growth during socket rehabilitation but
Publikováno v:
Journal of Medical Systems
This paper presents a methodological procedure, based on the anatomical reconstruction and constrained deformation, to design custom-made implants for forehead augmentation in people affected by Apert syndrome, experiencing a frontal bone deficiency.