Results 31 to 40 of about 15,266 (165)

Amelogenesis imperfecta: A clinician′s challenge

Journal of Indian Society of Pedodontics and Preventive Dentistry, 2012
Defective enamel formation can be explained as defects occurring at the stages of enamel formation. Quantitative defects in matrix formation leads to hypoplastic form of amelogenesis imperfecta.
V Chamarthi, B R Varma, M Jayanthi
doaj   +1 more source

Periodontal and orthodontic management of impacted canines

Periodontology 2000, EarlyView.
Abstract The maxillary and mandibular canines are described by many clinicians as the “cornerstone” of the arch. When in their optimal position, they play a critical role in providing a well‐balanced occlusal scheme that contributes toward functional as well as neuromuscular stability, harmony, esthetics, and dentofacial balance.
Mohammad Qali, Chenshuang Li, Chun‐Hsi Chung, Nipul Tanna   +3 more
wiley   +1 more source

Tratamiento rehabilitador en Amelogénesis Imperfecta [PDF]

, 2015
La amelogénesis imperfecta es una anomalía poco frecuente que afecta psíquicamente a los individuos que la presentan. Dada la importancia del restablecimiento integral de estos individuos a la sociedad nos decidimos a realizar un tratamiento ...
Casanova Rivero, Yanett, Cruz Gutiérrez, José Manuel, Álvarez Llanes, Marina, Lima Álvarez, Magda   +3 more
core  

Definition and recommendations for trial methods for evaluating dentin hypersensitivity: A hybrid AI‐assisted scoping review and Delphi consensus process

Periodontology 2000, EarlyView.
Abstract Background Dentin hypersensitivity (DH) is a common yet inconsistently defined condition impacting oral health and quality of life. Variability in diagnostic criteria and trial methodologies has limited comparability of previous research. Objectives To map current definitions, diagnostic frameworks, and clinical trial methodologies in DH ...
Alexander J. Pollard, Tom J. Pollard, Anne‐Marie Glenny, Jan Clarkson, Tanya Walsh, Maria Davies, Thomas Sounack, Matthew Wright, Joon Seong, Joshua Twigg, Rupert Austin, Rossana Izzetti, Crystal Marruganti, Robert Newcombe, Rebecca Bullock, Nicola X. West   +15 more
wiley   +1 more source

Association Between Hypomineralisation of Second Primary Molars and Tooth Agenesis

International Journal of Paediatric Dentistry, Volume 36, Issue 6, Page 883-889, November 2026.
ABSTRACT Background Hypomineralisation of second primary molars (HSPM) is an enamel defect with a multifactorial and potentially genetic aetiology. While the association between enamel defects and dental anomalies is a relatively recent area of investigation, it has not yet been explored specifically in cases of HSPM.
Débora Juliana de Araújo Lopes, Eloisa Cesario Fernandes, Jaderson Felipe Santos Dantas, Patrícia Bittencourt Santos   +3 more
wiley   +1 more source

WDR72 Promotes Neuroblastoma Stemness and Progression by Sequestering TRIM31‐Mediated Degradation of CBX8

Advanced Science, Volume 13, Issue 56, 9 October 2026.
This study unveiled that METTL14 mediates m6A modification of WDR72 mRNA to stabilize and enhance WDR72 expression, which disrupts TRIM31‐mediated ubiquitination of CBX8 protein and retards its degradation, finally the elevated CBX8 contributes to tumor stemness.
Huijuan Zeng, Zijie Ye, Manna Zheng, Jing Pan, Tianbao Tan, Jiliang Yang, Jiahao Li, Zhang Zhao, Tianzhu Long, Liyu Zhang, Gautam Sethi, Tianyou Yang, Chao Hu, Yan Zou   +13 more
wiley   +1 more source

Diagnosis, treatment planning, and full-mouth rehabilitation in a case of amelogenesis imperfecta

Contemporary Clinical Dentistry, 2018
Amelogenesis imperfecta is a genetic condition affecting the teeth resulting in aberrations of the structure and clinical appearance of enamel. The treatment of amelogenesis imperfecta involves a multidisciplinary treatment approach requiring a ...
Mayuri Naik, Siddharth Bansal
doaj   +1 more source

Dentofacial Characteristics in Patients With Epidermolysis Bullosa—A Cross‐Sectional Study

Clinical and Experimental Dental Research, Volume 12, Issue 5, October 2026.
ABSTRACT Objectives Epidermolysis bullosa (EB) is a rare genetic disease characterized by skin and mucosal fragility caused by pathogenic variants in structural protein genes. Malocclusions have been previously described in patients with EB, mainly in case reports, with no cohort studies characterizing dentofacial characteristics across all EB types ...
Sebastián Véliz, Susanne Krämer, Colomba Besa‐Witto, Pedro Diz‐Dios   +3 more
wiley   +1 more source

In Vitro Effects of Combining Resin Infiltration and At‐Home Bleaching on Hydrogen Peroxide Penetration, Color Change and Enamel Morphology

Journal of Esthetic and Restorative Dentistry, Volume 38, Issue 10, Page 1947-1956, October 2026.
ABSTRACT Objective To evaluate the effect of resin infiltration (RI) prior to at‐home bleaching on hydrogen peroxide (HP) penetration into the pulp chamber, color change, and enamel morphology in human teeth with sound enamel or white spot lesions (WSLs), using different RI protocols.
Bruno Baracco, Taynara S. Carneiro, Michel Wendlinger, Michael W. Favoreto, Laura Ceballos, Alessandro D. Loguercio   +5 more
wiley   +1 more source

Amelogenesis imperfecta

Orphanet Journal of Rare Diseases, 2007
Amelogenesis imperfecta (AI) represents a group of developmental conditions, genomic in origin, which affect the structure and clinical appearance of enamel of all or nearly all the teeth in a more or less equal manner, and which may be associated with ...
Aldred Michael, Bloch-Zupan Agnes, Crawford Peter JM   +2 more
doaj   +1 more source