Results 41 to 50 of about 36,048 (304)

Whole exome sequencing in an Italian family with isolated maxillary canine agenesis and canine eruption anomalies [PDF]

open access: yes, 2018
Objective: The aim of this study was the clinical and molecular characterization of a family segregating a trait consisting of a phenotype specifically involving the maxillary canines, including agenesis, impaction and ectopic eruption, characterized by ...
Barbato, Ersilia   +12 more
core   +1 more source

Relationship of the Morphology and Size of Sella Turcica with Dental Anomalies and Skeletal Malocclusions

open access: yesDiagnostics, 2023
This study aimed to assess the relationship of the morphology and size of the sella turcica (ST) with dental anomalies and skeletal malocclusions. This cross-sectional study was conducted on records of fixed orthodontic patients treated between 2013 and ...
Omid Mortezai   +7 more
doaj   +1 more source

Wear of human teeth: a tribological perspective [PDF]

open access: yes, 2005
The four main types of wear in teeth are attrition (enamel-on-enamel contact), abrasion (wear due to abrasive particles in food or toothpaste), abfraction (cracking in enamel and subsequent material loss), and erosion (chemical decomposition of the tooth)
Amaechi B. T.   +18 more
core   +2 more sources

Multimodal Wearable Biosensing Meets Multidomain AI: A Pathway to Decentralized Healthcare

open access: yesAdvanced Science, EarlyView.
Multimodal biosensing meets multidomain AI. Wearable biosensors capture complementary biochemical and physiological signals, while cross‐device, population‐aware learning aligns noisy, heterogeneous streams. This Review distills key sensing modalities, fusion and calibration strategies, and privacy‐preserving deployment pathways that transform ...
Chenshu Liu   +10 more
wiley   +1 more source

Mesiodens preventing eruption of a permanent central incisor [PDF]

open access: yes, 2005
A maxillary midline supernumerary tooth is the most common type of supernumerary tooth. We present a case of a mesiodens, preventing eruption of a permanent central incisor.
Azzopardi, Alexander   +2 more
core  

Seeing Through the Face: Robust Facial Diagnosis Enhanced by Landmark Detection and Pose Normalization

open access: yesAdvanced Intelligent Systems, EarlyView.
This study proposes a robust, generalizable new approach for facial type diagnosis. Based on landmark detection and pose normalization, a 94.7% diagnostic accuracy is achieved by Combined Heatmap Regression and Coordinate Regression network. This research makes the AI‐generated preliminary diagnosis more interpretable and reducing the impact of ...
Qianyang Xie   +12 more
wiley   +1 more source

Anomalous dental morphology and root resorption during orthodontic treatment: a pilot study

open access: yesAustralasian Orthodontic Journal, 1998
The present study investigated the relation between anomalous dental morphology and root resorption during orthodontic treatment. One hundred and eleven sets of orthodontic records (a total of 1,630 teeth) were examined.
Thongudomporn Udom, Freer Terrence J
doaj   +1 more source

Prevalence of Dental Anomalies in a Sample of Orthodontic Patients in Erbil City

open access: yesSulaimani Dental Journal, 2020
Objective: Dental anomalies are abnormal morphological development of dentition during various periods of tooth development and have an important role in the development of various kinds of malocclusions.
Asma Rahman   +2 more
doaj   +1 more source

Interaction between IRF6 and TGFA Genes Contribute to the Risk of Nonsyndromic Cleft Lip/Palate [PDF]

open access: yes, 2012
Previous evidence from tooth agenesis studies suggested IRF6 and TGFA interact. Since tooth agenesis is commonly found in individuals with cleft lip/palate (CL/P), we used four large cohorts to evaluate if IRF6 and TGFA interaction contributes to CL/P ...
Alexandre R. Vieira   +18 more
core   +5 more sources

Swallowing and Communication in Cockayne Syndrome: Clinical Characteristics and Management

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cockayne syndrome (CS) is an ultrarare genetic disorder associated with genes encoding proteins involved in DNA repair. The clinical course of CS involves neurodevelopmental and neurodegenerative features, including swallowing and communication impairments.
Abigail M. Spoden   +2 more
wiley   +1 more source

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