Results 41 to 50 of about 45,660 (205)

Relationship among malocclusion, number of occlusal pairs and mastication [PDF]

open access: yes, 2010
This study evaluated the relationship among malocclusion, number of occlusal pairs, masticatory performance, masticatory time and masticatory ability in completely dentate subjects.
CURY, Altair Antoninha Del Bel   +5 more
core   +2 more sources

Using Propensity Score Subclassification to Estimate the Population‐Average Causal Effect of Temporomandibular Dysfunction Experience on Oral Health‐Related Quality of Life Among Australian Adults

open access: yesCommunity Dentistry and Oral Epidemiology, Volume 53, Issue 3, Page 265-277, June 2025.
ABSTRACT Background Temporomandibular dysfunction (TMD) experience might impair oral health‐related quality of life (OHRQoL). Causal inference using population‐based cross‐sectional data is challenging given the potential for bias. Propensity Score Subclassification (PS‐Subclassification) provides a tool to mitigate confounding bias.
Kamal Hanna   +4 more
wiley   +1 more source

Influence of ceramic (feldspathic) surface treatments on the micro-shear bond strength of composite resin [PDF]

open access: yes, 2010
Objective: To test the null hypothesis that surface treatment has no influence on the micro-shear bond strength between orthodontic composite resin cement and ceramics (feldspathic porcelain).
Borges, Gilberto Antonio   +3 more
core   +1 more source

Progress in Translating Glaucoma Genetics Into the Clinic: A Review

open access: yesClinical &Experimental Ophthalmology, Volume 53, Issue 3, Page 246-259, April 2025.
ABSTRACT Precision medicine is paving the way for personalised risk assessment, and its translation into glaucoma clinics holds potential to change current management paradigms. Our understanding of glaucoma's genetic architecture has expanded in recent years, recognising both monogenic and polygenic contributions.
Antonia Kolovos   +3 more
wiley   +1 more source

Induced Ankylosis of a Primary Molar for Skeletal Anchorage in the Mandible as Alternative to Mini-Implants [PDF]

open access: yes, 2015
Background Mesial protraction of mandibular posterior teeth requires increased anchorage to avoid undesired tooth movements. Orthodontic mini-implants have become a popular and successful way to increase skeletal anchorage in such cases.
Angelopoulou, Matina V.   +3 more
core   +2 more sources

Aarskog Syndrome: Deep Phenotyping and Genomic Landscape of a New Cohort Including Adult Patients

open access: yesClinical Genetics, EarlyView.
This study presents the deep phenotyping data of 14 new Aarskog‐Scott syndrome patients with molecular confirmation. ABSTRACT Aarskog‐Scott syndrome (AAS, MIM#305400) is an X‐linked disorder characterized by recognizable facial features, short stature, and genitourinary and skeletal malformations.
Gozde Tutku Turgut   +7 more
wiley   +1 more source

A Novel Intronic Variant in the KH3 Domain of HNRNPK Leads to a Mild Form of Au‐Kline Syndrome

open access: yesClinical Genetics, EarlyView.
Integrated genomic and epigenomic analyses, associated with functional studies, confirm the pathogenicity of a novel HNRNPK variant in Au‐Kline syndrome (AKS). Our study underscores the value of DNA methylation signatures in variant interpretation, enhancing accurate diagnosis and clinical management of rare neurodevelopmental disorders.
Maura Mingoia   +16 more
wiley   +1 more source

Comparative anchorage maintenance between the intercanine coil, lip bumper, and mandibular cervical traction during cuspid retraction [PDF]

open access: yes, 1972
Thesis (M.Sc.D.)--Boston University School of Graduate Dentistry, 1972 (Orthodontics)Bibliography included.The present study was undertaken to compare the efficiency of three different biomechanical mechanisms in preserving mandibular molar anchorage ...
Iverson, Dennis B.
core  

Delayed eruption of permanent dentition and maxillary contraction in patients with cleidocranial dysplasia: review and report of a family [PDF]

open access: yes, 2018
Introduction. Cleidocranial dysplasia (CCD) is an inherited disease caused by mutations in the RUNX2 gene on chromosome 6p21. This pathology, autosomal dominant or caused by a spontaneous genetic mutation, is present in one in one million individuals ...
Barbato, E.   +5 more
core   +2 more sources

Malocclusion of the temporary teeth [PDF]

open access: yesInternational Journal of Orthodontia, 1915
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openaire   +3 more sources

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