Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Abel Cahuana"'
Autor:
Pau Cahuana-Bartra, Abel Cahuana-Cárdenas, Lluís Brunet-Llobet, Marta Ayats-Soler, Jaume Miranda-Rius, Alejandro Rivera-Baró
Publikováno v:
3D Printing in Medicine, Vol 6, Iss 1, Pp 1-10 (2020)
Abstract Background In medicine and dentistry, 3D technology allows the virtual planning and printing of surgical replicas of anatomical structures that can facilitate certain transplant procedures. In dentistry, 3D technology is useful in autogenous
Externí odkaz:
https://doaj.org/article/ded4dd46d33b40e384d73e96b3a378f5
Autor:
Carla Munné-Miralvés, Lluís Brunet-Llobet, Abel Cahuana-Cárdenas, Sergi Torné-Durán, Jaume Miranda-Rius, Alejandro Rivera-Baró
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)
Abstract Introduction Prader-Willi Syndrome (PWS) is a genetic disorder caused by the lack of expression of certain paternal genes located on chromosome 15q11-q13. This anomaly causes cognitive, neurological and endocrine abnormalities, among which o
Externí odkaz:
https://doaj.org/article/e4a4ac76efc8498a8ee90c78da8a8ab4
Publikováno v:
Case Reports in Dentistry, Vol 2014 (2014)
Fused teeth may cause aesthetic, spacing, periodontal, eruption, and caries problems. The present case report describes a 7-year-old boy patient with a chief complaint of unerupted maxillary incisor. Radiographic examination indicated a fused tooth w
Externí odkaz:
https://doaj.org/article/43708926d0e44d8d9fab568f751c8a01
Autor:
Lluís Brunet-Llobet, Abel Cahuana-Cárdenas, Alejandro Rivera-Baró, Jaume Miranda-Rius, Carla Munné-Miralvés, Sergi Torné-Duran
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-7 (2020)
Orphanet Journal of Rare Diseases
Dipòsit Digital de la UB
Universidad de Barcelona
Orphanet Journal of Rare Diseases
Dipòsit Digital de la UB
Universidad de Barcelona
Introduction Prader-Willi Syndrome (PWS) is a genetic disorder caused by the lack of expression of certain paternal genes located on chromosome 15q11-q13. This anomaly causes cognitive, neurological and endocrine abnormalities, among which one of the
Autor:
Abel Cahuana-Cárdenas, Lluís Brunet-Llobet, Javier Martín de Carpi, Jaume Miranda-Rius, Alejandro Rivera-Baró, Sandra Cardona-Soria
Publikováno v:
Special Care in Dentistry. 40:35-40
Aims Cerebral palsy (CP) is a chronic, nonprogressive disorder affecting movement, posture, and tone, caused by injuries in the central nervous system during the early stages of life. Patients with CP have swallowing disorders, which make oral feedin
Autor:
Jaume Miranda-Rius, Lluís Brunet-Llobet, Abel Cahuana-Cárdenas, Alejandro Rivera-Baró, Marta Ayats-Soler, Pau Cahuana-Bartra
Publikováno v:
3D Printing in Medicine
3D Printing in Medicine, Vol 6, Iss 1, Pp 1-10 (2020)
3D Printing in Medicine, Vol 6, Iss 1, Pp 1-10 (2020)
Background In medicine and dentistry, 3D technology allows the virtual planning and printing of surgical replicas of anatomical structures that can facilitate certain transplant procedures. In dentistry, 3D technology is useful in autogenous tooth tr
Publikováno v:
Journal of Clinical Pediatric Dentistry. 33:155-160
Destructive forms of periodontal disease in children are uncommon. Severe periodontal destruction can be a manifestation of a systemic disease; however, in some patients, the underlying cause of increased susceptibility and early onset is still unkno
Autor:
Joan Ramon Boj Quesada, Abel Cahuana Cárdenas, Luciana Butini Oliveira, José Enrique Espasa Suarez de Deza, Gabriela Mesquita Lopes-Freire, Josep Maria Ustrell-Torrent
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Progress in Orthodontics
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Progress in Orthodontics
Background This study aimed to explore the association between feeding habits, non-nutritive sucking habits, and malocclusions in deciduous dentition. Methods A cross-sectional observational survey was carried out in 275 children aged 3 to 6 years an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cf584b4438a0172adf6e1f56892040e
http://hdl.handle.net/2445/127329
http://hdl.handle.net/2445/127329
Publikováno v:
Case Reports in Dentistry, Vol 2014 (2014)
Recercat. Dipósit de la Recerca de Catalunya
instname
Case Reports in Dentistry
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Case Reports in Dentistry
Dipòsit Digital de la UB
Universidad de Barcelona
Fused teeth may cause aesthetic, spacing, periodontal, eruption, and caries problems. The present case report describes a 7-year-old boy patient with a chief complaint of unerupted maxillary incisor. Radiographic examination indicated a fused tooth w
Publikováno v:
Medicina oral, patologia oral y cirugia bucal. 13(12)
Prader Willi Syndrome (PWS) is a relatively rare neurogenetic illness. It is of interest to dentists for its clinical characteristics. The aim of this study was to evaluate the amount of saliva and the presence of Streptococcus mutans (St mutans) in