Results 41 to 50 of about 31,523 (289)

Dental anomalies in craniofacial microsomia: A systematic review [PDF]

open access: yes, 2019
Objective: To provide an overview on the prevalence and types of dental anomalies in patients with craniofacial microsomia (CFM). Eligibility criteria: Inclusion criteria were CFM and dental anomalies.
Dunaway, D.J. (David)   +5 more
core   +3 more sources

Dental number anomalies [PDF]

open access: yes, 2022
Introduction. Dental number anomalies are a part of dental system anomalies, represented by hypodontics and hyperdontics. Dental number anomalies are one of the most important problems of dentistry, because the frequency of patients with these ...
Popa, Gabriela
core  

Dental developmental anomalies and post-eruption dental disorder

open access: yes, 2021
Panoramic radiographs are complementary exams to evaluate oral alterations in an early manner, these changes can be dental developmental anomalies, and post-eruption dental disorder.
Alina Nunes Braga   +13 more
core   +1 more source

Prevalence of Dental Anomalies in a Sample of Turkish Children: A Retrospective Study [PDF]

open access: yes
Objective: The aim of this study was to determine the prevalence of dental anomalies in Turkish children aged 2-14 years by panoramic radiographies. The most common dental anomaly, the frequency of multiple dental anomalies and gender differences were ...
Pınar SERDAR EYMİRLİ   +2 more
core   +1 more source

Prevalence of dental anomalies in a group of Turkish people

open access: yes, 2023
Aim Dental anomalies in tooth number, shape, and position usually result in aesthetic and functional problems. These anomalies can affect both primary teeth and permanent teeth.
Kendirci, Merve Yelken   +2 more
core  

Variability, asymmetry and sexual dimorphism in craniofacial anomalies in Loeys-Dietz syndrome 2: geometric morphometric analysis in mice

open access: yesScientific Reports
Loeys-Dietz syndrome is a rare connective tissue disorder characterized by life-threatening aortic aneurysm and distinctive craniofacial anomalies. It is caused by mutations along the transforming growth factor beta (TGF-β) signaling pathway (LDS1-6). We
Katelin R. Devine   +11 more
doaj   +1 more source

Resin-bonded fixed partial denture as a cost-effective prosthesis for missing maxillary lateral incisor in a cleft lip and palate patient: a case report

open access: yes, 2022
Literature suggests 66.7% of dental abnormalities among patients with cleft lip and palate (CLP). Besides posing functional difficulties, dental anomalies also raise significant aesthetic concerns among these patients, especially with missing teeth in ...
Sajjan MC, Suresh   +5 more
core   +1 more source

ERK‐Mediated Phosphorylation of YAP Defines a Noncanonical FGF Signaling Mechanism in Stem Cells

open access: yesAdvanced Science, EarlyView.
With a powerful combination of in vivo, ex vivo, and in vitro models, the authors highlight a novel FGF‐ERK signaling regulation of YAP at the S128 site in neural crest‐derived stem cells. This study opens exciting new directions in stem cell biology and craniofacial biology, paving the way for potential innovations in the treatment of craniofacial ...
Xiaolei Zhao   +16 more
wiley   +1 more source

Acute hyperlipidemia has transient effects on large-scale bone regeneration in male mice

open access: yesScientific Reports
Excessive dietary fat intake increases plasma lipid levels and has been associated with reduced bone mineral density (BMD) and increased risk of osteoporotic fracture, especially in older postmenopausal women.
Luciana Yamamoto de Almeida   +3 more
doaj   +1 more source

Expanding the Phenotype of TUFM‐Related Combined Oxidative Phosphorylation Deficiency 4

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Combined oxidative phosphorylation deficiency 4 (COXPD4) is a rare mitochondrial condition caused by biallelic deleterious variants in the nuclear‐encoded gene TUFM. To date, most individuals with COXPD4 have presented with encephalopathy, hypotonia, and abnormal brain imaging. Many of the reported individuals died in infancy. We aim to expand
Noémie Villeneuve‐Cloutier   +2 more
wiley   +1 more source

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