Results 261 to 270 of about 257,740 (355)

The COVID-19 post-pandemic scenario to Oral Radiology at Dental Schools. [PDF]

Oral Radiol, 2020
Rosa BSPA, Ferreira MD, Moreira GC, Bastos MF, Pinto RR, Visconti MA, Junqueira RB, Verner FS.   +7 more
europepmc   +1 more source

A Study on Between-Meal Eating Habit from the Viewpoint of Dental Health-Comparison with Primary School Children and the Relationship between the Habit and Dental Caries.

, 1996
Masafumi Motohashi, Koji Ozawa, Toru SAGARA   +2 more
openalex   +2 more sources

Validating the Measurement Tool of Dental School Environment Satisfaction [PDF]

, 2003
Sun Kim, Hye Sook Kim
openalex   +1 more source

Exploring Oral Health Related Quality of Life in Rett Syndrome Using Directed Content Analysis

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT No validated oral health‐related quality of life (OHRQOL) instrument currently exists for those with severe intellectual and developmental disabilities and who communicate non‐verbally. This qualitative study aimed to explore the domains that were important to the oral health‐related quality of life in individuals with Rett syndrome (RTT).
Yvonne Yee Lok Lai, Jenny Anne Downs, Helen Margaret Leonard, Laurence James Walsh, Sobia Zafar   +4 more
wiley   +1 more source

Oral radiology practice in dental schools during the COVID-19 pandemic: What will be the new normal? [PDF]

Imaging Sci Dent, 2020
Fontenele RC, Gomes AF, Freitas DQ.
europepmc   +1 more source

Interrelationship between the dental functions and physical fitness, motor ability and physique of junior high school girls

, 2000
Hiroko Munetaka, Kazutoshi Kikkawa, Tatsuo Yamaguchi   +2 more
openalex   +2 more sources

The context of a dental school in Africa

African Journal of Oral Health Sciences, 2004
openaire   +3 more sources

Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Gorlin‐Goltz Syndrome (GGS) is a rare autosomal dominant genetic disorder encompassing a diverse range of clinical manifestations, including congenital anomalies and predisposition to cancer. Pathogenic variants in PTCH1 and SUFU account for up to 79% and 6% of cases, respectively. Currently, an estimated 15%–27% of individuals with a clinical
V. Taliercio, J. Zhao, S. E. Boyden, R. Mao, P. Bayrak‐Toydemir, A. Pflaum, J. Palumbos, A. Andrews, E. E. Baldwin, C. Welt, Mackenzie Fait, Undiagnosed Diseases Network, L. D. Botto, D. Viskochil   +13 more
wiley   +1 more source

Dental caries and periodontal conditions among primary school children in Morogoro municipality, Tanzania

, 2001
Emil N. Kikwilu, G.J. Mandari
openalex   +2 more sources

Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The interstitial 6p microdeletion syndrome is characterized by dysmorphic facies and structural heart, kidney, brain, and musculoskeletal differences. RREB1 haploinsufficiency and consequent abnormal RAS‐MAPK pathway signaling have been proposed as a driver of the disease phenotype; however, apart from a single case report, the phenotype of ...
Alanna Strong, Caoimhe McKenna, Karen Stals, Antonio Vitobello, Mathilde Renaud, Claudine Rieubland, Michel Guipponi, Christophe Philippe, Paul Vrana, Alisa Gaskell, A. Micheil Innes, Alyssa L. Rippert, Rebecca Ahrens‐Nicklas, Elizabeth Bhoj, Kiersten Keller, Bimal P. Chaudhari, Brandon S. Stone   +16 more
wiley   +1 more source