Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Manuel Joaquín De Nova"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-10 (2024)
Abstract Background Osteogenesis imperfecta (OI) affects dental and craniofacial development; therefore, it can influence oral health-related quality of life (OHRQoL). The objective of this study was to explore the influence of the severity of OI on
Externí odkaz:
https://doaj.org/article/8e620182fe7246c6a57bfa7a62eefb07
Autor:
Antonia M. Caleya, Andrea Martín-Vacas, Gonzalo Feijóo, Maria Rosa Mourelle-Martínez, Manuel Joaquín de Nova-Garcia, Nuria E. Gallardo-López
Publikováno v:
Education Sciences, Vol 14, Iss 8, p 874 (2024)
Collaborative learning (CL) is the instructional use of small groups in such a way that students work together to maximize their own and others’ learning. In this study, the aim was to implement online collaborative learning (OCL) using the Microso
Externí odkaz:
https://doaj.org/article/525363a4d06048d19ab3a47328cfab94
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/f757c0a38e384e5a86484354a90ebdeb
Publikováno v:
Applied Sciences, Vol 14, Iss 5, p 1954 (2024)
Osteogenesis imperfecta is a disorder characterized by osteopenia and bone fragility. Considering that orthopantomography is a routine diagnostic test in growing patients, it can be used to analyze bone density in these patients. The study sample con
Externí odkaz:
https://doaj.org/article/df25e32540044ff5aa92b1fe1be5095c
Publikováno v:
Applied Sciences, Vol 14, Iss 4, p 1640 (2024)
Osteogenesis Imperfecta (OI) is a genetic disease characterized by osteopenia and bone fragility in which the craniocervical junction is also affected. This is of special relevance due to the high prevalence in anomalies described in the literature a
Externí odkaz:
https://doaj.org/article/2590960c3168453c810db0f3663aa68c
Autor:
Andrea Martín-Vacas, Vicente Vera-González, Julio Ramírez-Castellanos, Diego González-Gil, Manuel Joaquín de Nova García
Publikováno v:
Applied Sciences, Vol 13, Iss 22, p 12451 (2023)
The aim is to quantitatively analyze the diameter and tubular density and semi-quantitatively analyze the elemental composition (Calcium and Phosphorus) in the dentin of primary teeth of children with Osteogenesis Imperfecta (OI) in comparison with a
Externí odkaz:
https://doaj.org/article/db66ac25fd0b49eea4896e1627b97224
Publikováno v:
Children, Vol 10, Iss 6, p 1029 (2023)
Osteogenesis Imperfecta (OI) is a disease that causes bone fragility and deformities, affecting both the cranial base and the craniocervical junction, and may lead to other neurological disorders. A retrospective cross-sectional study was carried out
Externí odkaz:
https://doaj.org/article/a68fb67c460a4e25b3ef2402ec7e5711
Publikováno v:
Children; Volume 10; Issue 6; Pages: 1029
Osteogenesis Imperfecta (OI) is a disease that causes bone fragility and deformities, affecting both the cranial base and the craniocervical junction, and may lead to other neurological disorders. A retrospective cross-sectional study was carried out
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::03ffe161b48cd215ac7757ff4fe4e20d
Autor:
Víctor, Cortezo, Carlos M, Cobo-Vázquez, Alfonso, Rayo, Félix M, Martín, Tomás, Hernán, Víctor M, Paredes, Manuel Joaquín, De Nova
Publikováno v:
Quintessence international (Berlin, Germany : 1985).
There is a high demand for dental treatment in a hospital setting for patients with severe intellectual disability (ID), due to their inability to cooperate. The objective was to determine the types of dental treatment carried out on patients with se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ebf9883a958bf996b4bdc172d7cdb590
https://pubmed.ncbi.nlm.nih.gov/36378299
https://pubmed.ncbi.nlm.nih.gov/36378299
Autor:
Andrea Martín-Vacas, Manuel Joaquín de Nova, Belén Sagastizabal, Álvaro Enrique García-Barbero, Vicente Vera-González
Publikováno v:
Healthcare; Volume 10; Issue 8; Pages: 1453
Background: Dentinogenesis imperfecta type I (DGI-I) is a hereditary alteration of dentin associated with osteogenesis imperfecta (OI). Aim: To describe and study the morphological characteristics of DGI-I with scanning electron microscopy (SEM). Mat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::231d0b44f8c5c8d3a2787b5dc2805e45