Results 71 to 80 of about 4,126 (210)

Skeletal and Dental‐Alveolar Changes With Invisalign First Expansion System in the Mixed Dentition: A Retrospective Study

open access: yesOrthodontics &Craniofacial Research, Volume 29, Issue 2, Page 237-246, April 2026.
ABSTRACT Background This retrospective study aimed to evaluate the skeletal and dentoalveolar effects of maxillary expansion using the Invisalign First system in the mixed dentition. Methods The study was conducted in the orthodontic department of the Fourth Affiliated Hospital of Zhejiang University School of Medicine between 2021 and 2024.
Qi Wang   +4 more
wiley   +1 more source

Quantifying Root Resorption on the Incisors After Clear Aligner and Fixed Appliance Therapy Using Artificial Intelligence Tool Based CBCT Surface Models: Randomized Clinical Trial

open access: yesOrthodontics &Craniofacial Research, Volume 29, Issue 2, Page 366-374, April 2026.
ABSTRACT Objective To quantify external apical root resorption (EARR) on the incisors following non‐extraction treatment of Class I malocclusion patients with moderate crowding, comparing clear aligners and fixed appliances using a novel 3D analysis of Cone‐Beam Computed Tomography (CBCT) derived surface models.
Roberto Bespalez‐Neto   +6 more
wiley   +1 more source

Application of New Appliances for Management of Growing Class III Malocclusion Child: Comparazation Case Reports

open access: yes치위생과학회지, 2020
The purpose of this comparison of case reports is to introduce the results of the application of new devices for the management of growing Class III malocclusions in children. Two 8-year-old boys had a chief complaint of anterior crossbite.
So-Youn An   +3 more
doaj   +1 more source

Spatial Transcriptomics of TMJ Reveals a Remodeling Fibroblast‐Immune Microenvironment Driving Arthritis Pain

open access: yesAdvanced Science, Volume 13, Issue 18, 27 March 2026.
Spatial transcriptomics reveals a remodeled fibroblast‐immune microenvironment in the temporomandibular joint (TMJ) during arthritis. By combining seqFISH with genetic mouse models, this study uncovers TMJ spatial cell atalas, macrophage‐fibroblast crosstalk, and cytokine signaling pathways driving TMJ inflammation and pain.
Ziying Lin   +10 more
wiley   +1 more source

Interceptive Treatment of Anterior Crossbite: Case series

open access: yesBIRTH AND GROWTH MEDICAL JOURNAL, 2018
NASCER E CRESCER - BIRTH AND GROWTH MEDICAL JOURNAL, Vol 27, No 2 (2018)
Pinho, Teresa   +2 more
openaire   +4 more sources

Nance‐Horan Syndrome: Further Delineation of the Affected Male and the Female Carrier Phenotypes

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 642-652, March 2026.
ABSTRACT Nance‐Horan syndrome (NHS; OMIM 302350) is a rare, X‐linked syndrome characterized by bilateral congenital cataracts leading to profound vision loss, specific dental anomalies including characteristic screwdriver blade‐shaped incisors, facial anomalies, and intellectual disability.
Maria K. Haanpää   +14 more
wiley   +1 more source

Intervention Of Anterior Crossbite With Concomitant Unilateral Posterior Locked Occlusion

open access: yesInternational Dental Journal
Introduction: Pediatric anterior crossbite with unilateral posterior locked occlusion not only impairs chewing function and increases risk of TMJ disorders, but may also disrupt craniofacial development.
Li Runhang   +3 more
doaj   +1 more source

Early Treatment Of Anterıor Cross-Bıte: A Case Report

open access: yesTurkish Journal of Orthodontics, 2004
Anterior crossbite can be a result of skeletal, functional or dental disharmony of the the orthognathic system. Removable and fixed appliances are widely used methods to correct them.
Elçin Esenlik, M. Okan Akçam
doaj   +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, Volume 200, Issue 3, Page 661-672, March 2026.
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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