Results 31 to 40 of about 45,033 (364)

Immediate anterior tooth replacement by using an esthetic fixed bridge: A case report

open access: yesMedicina Clínica Práctica, 2020
Introduction: Loss of teeth due to extraction is often found in some cases. Preserving interproximal soft tissue and preventing alveolar bone from collapse due to tooth extraction is the most challenging issue. Ovate pontic design can give a natural look
Muhammad Ikbal   +3 more
doaj   +1 more source

Retrospective analysis of the correlation between the facial biotype and the inclination of the upper canine cusp axis to the occlusal plane [PDF]

open access: yes, 2016
Permanent maxillary canines are the second most frequently impacted teeth and the prevalence of this clinical condition is estimated to be 1-2% in the general population.
Cielo, A.   +4 more
core   +1 more source

[A two-rooted maxillary incisor]. [PDF]

open access: yesNederlands tijdschrift voor tandheelkunde, 2006
A case report is presented of a 14-year-old girl with a buccoapical fistula of tooth 22. The radiograph of the tooth revealed a periapical radiolucency and two roots. Endodontic treatment was conducted, followed by normal healing of the periapical area. Root division and additional roots of maxillary lateral incisors are rare phenomena.
Drent, T., Baat, C. de
openaire   +2 more sources

Moving an incisor across the midline: A treatment alternative in an adolescent patient [PDF]

open access: yes, 2011
A 13-year-old sought treatment for a severely compromised maxillary left central incisor and an impacted fully developed left canine. Extraction of both teeth became necessary.
Bosio, Jose A   +2 more
core   +1 more source

Talon cusp affecting primary dentition in two siblings: a case report [PDF]

open access: yes, 2014
The term talon cusp refers to a rare developmental dental anomaly characterized by a cusp-like structure projecting from the cingulum area or cement-enamel junction.
King, N. M.   +3 more
core   +1 more source

Synaptic Dysfunction in the Anterior Cingulate Cortex Underlies Pain‐Anxiety Comorbidity in a Mandibular Asymmetry Mouse Model

open access: yesAdvanced Science, EarlyView.
This study establishes a mandibular asymmetry (MA) mouse model that recapitulates chronic orofacial pain and anxiety comorbidity. Anterior cingulate cortex (ACC) hyperactivation and synaptic dysfunction are identified as central neural mechanisms underlying these pathologies, with chemogenetic inhibition of ACC CaMKII+ neurons effectively reversing ...
Zhaoyichun Zhang   +19 more
wiley   +1 more source

Bilateral fusion of permanent maxillary incisors

open access: yesIndian Journal of Dental Research, 2011
Dental fusion is a rare developmental anomaly, which is included in the anomalies of tooth morphology or shape. Fusion can occur at the level of enamel or enamel and dentin, which results in the formation of a single tooth with enlarged clinical crown. Fusion is more common in deciduous dentition.
Shashit Shetty   +2 more
openaire   +4 more sources

All‐In‐One Iontronic Sensing Aligner for High‐Precision 3D Orthodontic Force Monitoring

open access: yesAdvanced Science, EarlyView.
A wireless, battery‐free orthodontic sensing system is developed by integrating a cross‐shaped iontronic sensor and an origami‐inspired NFC circuit into clear aligners. This all‐in‐one device enables real‐time, in vivo 3D force monitoring with high precision and long‐term stability, providing clinicians with quantitative biomechanical feedback to ...
Jiahao Guo   +10 more
wiley   +1 more source

Quantification of three-dimensional orthodontic force systems of T-loop archwires [PDF]

open access: yes, 2010
Objective: To demonstrate the three-dimensional (3D) orthodontic force systems of three commercial closing T-loop archwires using a new method and to quantify the force systems of the T-loop archwires.
Brizendine, Edward J.   +2 more
core   +1 more source

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim   +9 more
wiley   +1 more source

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