Results 31 to 40 of about 58,049 (283)

Mechanics and Mathematical Modeling of Class III Treatment with Orthodontic Appliances with a Movable Ramp [PDF]

open access: yes, 2016
Treatment of class III is a current problem in orthodontics that requires constant improvement of its methods, development of new or modifications of known methods and techniques.
Doroshenko, N. (Nataliia)   +4 more
core   +2 more sources

Malocclusion Type and TDI Susceptibility in Adolescent

open access: yesAdvances in Human Biology
Introduction: Traumatic dental injuries (TDIs) are a significant concern in adolescent dental health, with malocclusion being a potential risk factor. Understanding the relationship between different types of malocclusion and the susceptibility to TDIs ...
Richa Shree   +5 more
doaj   +1 more source

The importance of screening in children who snore [PDF]

open access: yes, 2019
It is important to screen for OSAS in children who snore, as early treatment of OSAS can prevent neurocognitive, behavioural, cardiovascular and metabolic consequences.
Evangelisti, M., Villa, Mp
core   +1 more source

Lateral cephalometric analysis of asymptomatic volunteers and symptomatic patients with and without bilateral temporomandibular joint disk displacement [PDF]

open access: yes, 1998
Few studies of dentofacial and orthodontic structural relationships relative to temporomandibular joint (TMJ) dysfunction have been reported. We undertook this investigation to determine any correlation of orthodontic and dentofacial characteristics with
Beck, Frank M.   +4 more
core   +1 more source

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

Malocclusion among children in Vietnam: Prevalence and associations with different habits

open access: yesJournal of Oral Biology and Craniofacial Research
Background: This study aimed to measure the prevalence of malocclusion and identify associated factors among elementary school students in Vietnam. Method: A cross-sectional study was conducted from March to December 2022 at six primary schools located ...
Dung Anh Vu   +3 more
doaj   +1 more source

Prevailing Status and Treatment Seeking Awareness Among Patients Attending in The Orthodontics Department of Bangabandhu Sheikh Mujib Medical University

open access: yesBangabandhu Sheikh Mujib Medical University Journal, 2011
Background: Malocclusion is problem since antiquity. But people’s perception about the problem varies with their geographical location and cultural background. The problem seems to be more acute in developing countries like Bangladesh.
Tanzila Rafique   +3 more
doaj   +1 more source

Remote Language Assessment in School‐Age Children With Phelan–McDermid Syndrome and Genotype–Phenotype Correlation

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT People with Phelan–McDermid syndrome (PMS) have reduced speech and language abilities, yet little research has profiled the communication abilities in this population. The purpose of this study was threefold: identifying the language and communication profiles of school‐aged children with PMS, identifying genetic contributions to language and ...
Sarah Quadri‐Valverde   +12 more
wiley   +1 more source

Orthodontic treatment need and prevalence of malocclusions in the Orthodontic Unit of "Sapienza - University of Rome" : a six - year clinical experience [PDF]

open access: yes, 2019
AIM The objective of this epidemiological survey was to investigate the dental-skeletal features of subjects attending the Public Dental Service in U.O.C. (Orthodontic Department of “La Sapienza University of Rome) and compare them with the existing body
Giordano, Alessandra
core  

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet   +10 more
wiley   +1 more source

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