Results 161 to 170 of about 573,677 (352)

Dentofacial Malocclusion in Neurofibromatosis 1 in Finland

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Neurofibromatosis 1 (NF1) is an inherited disease that can be accompanied by oral health problems such as caries, periodontitis, and tumors affecting the oral cavity. Also, different maxillary and mandibular malformations are associated with NF1.
Vivian Reinhold, Mikko Valtanen, Kari Auranen, Stina Syrjänen, Sirkku Peltonen, Juha Peltonen, Roope A. Kallionpää   +6 more
wiley   +1 more source

Developments, application, and performance of artificial intelligence in dentistry – A systematic review

Journal of Dental Sciences, 2020
S. Khanagar, A. Al-Ehaideb, P. Maganur, S. Vishwanathaiah, S. Patil, H. Baeshen, S. Sarode, S. Bhandi   +7 more
semanticscholar   +1 more source

Dentistry: The Errant Branch. Shall Medicine Re-adopt It?

, 1932
Frederick T. van Beuren
openalex   +1 more source

Parental Communication With their Children about Cancer Risk and DTC Cascade Genetic Testing: Implications for Genetic Education and Counseling

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Cascade genetic testing for cancer risk can influence relatives' health outcomes, as they may benefit from risk reduction and screening. However, clinical guidelines discourage predictive genetic testing in childhood—including direct‐to‐consumer (DTC) testing.
Marcelo M. Sleiman Jr., Talia Zamir, Beth N. Peshkin, Jada G. Hamilton, Mingqian Liu, Mary Rose Yockel, Benjamin Wilfond, Lainie Friedman Ross, Jamie Brower, Hannah Ovadia, Rosalba Sacca, Beth Tarini, Susan M. Domchek, Claudine Isaacs, Kenneth P. Tercyak   +14 more
wiley   +1 more source

AN Introduction to the Chemical Analysis for Students of Medicine, Pharmacy and Dentistry. [PDF]

, 1902

openalex   +1 more source

Genotype–Phenotype Correlations, Mortality, and Clinical Insights in Keratitis–Ichthyosis–Deafness Syndrome: A Comprehensive Review and Case Report

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Keratosis–ichthyosis–deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American ...
Leslie Patrón‐Romero, Marco Antonio Hernández Lepe, José de Jesús Manríquez Torres, Diego Daniel Aguirre‐Gómez, Natsuo Hayashi‐Mercado, Genaro Rodríguez Uribe, Tadeo Cerón, María Ruiz‐Gamboa, Jesús Alonso Gándara‐Mireles, Ismael Lares‐Asseff, Verónica Loera‐Castañeda, Jorge Alvelais‐Palacios, Lucrecia Arzamendi‐Cepeda, Lidia Magdalena Castañeda‐González, Adolfo García‐Barrón, Francisco Yamal Quiroz Herrera, Francisco González‐Salazar, Horacio Almanza‐Reyes   +17 more
wiley   +1 more source

Dentistry and coronavirus (COVID-19) - moral decision-making

British Dental Journal, 2020
P. Coulthard
semanticscholar   +1 more source

Assessment of the Anatomical Position and Shape of Mental Foramen in the Cone Beam Computed Tomography Images

پزشکی بالینی ابن سینا, 2012
Introduction & Objective: The mental foramen is a part of lower jaw which has neurovascular bundles and also is important in biology. 3D imaging of this area by cone beam computed tomography (CBCT) before surgery can prevent some problems.
Amir Eskandarlo, Vahid Sartipi, Karim Ghazikhanlou Sani   +2 more
doaj  

Malignancy and its relation to dentistry

, 1927

openalex   +2 more sources

Pathology for Students of Dentistry [PDF]

, 1954

openalex   +1 more source