Results 131 to 140 of about 66,888 (302)

Prevalence of dental anomalies and enamel hypoplasia in primary dentition among preschool children of West Godavari District, Andhra Pradesh -A cross - sectional study

open access: yesJournal of Indian Association of Public Health Dentistry, 2013
Background: It is axiomatic that Pediatric dental anomalies and enamel hypoplasia (E.H) are routinely encountered in primary dentition and early detection and prudent management of the condition facilitates normal occlusal development.
Suzan Sahana   +5 more
doaj  

Investigating relationships among strontium, barium, and seasonality in wild baboons

open access: yesArchaeometry, EarlyView.
Abstract Geochemical profiles of Australopithecus africanus and baboon teeth show fluctuating trace elements, possibly reflecting seasonal diets. Here we use laser ablation–inductively coupled plasma–mass spectrometric measurements of calcium‐normalized strontium and barium ratios (Sr/Ca and Ba/Ca) and ion microprobe analyses of oxygen isotopes (δ18O ...
Maya Bharatiya   +12 more
wiley   +1 more source

Prevalence of Dental Anomalies in Adult Orthodontic Patients with Oral Radiological Point: A Systematic Review

open access: yesSudan Journal of Medical Sciences
Background: Dental rosy anomalies, although not a disease, can impact a person’s quality of life. This study investigates irregularities in the teeth, the degree of opening of the edge of the upper and lower teeth, and pink dental anomalies in the ...
Samareh Abbassi, Neda Tajbakhsh
doaj   +1 more source

Measuring the Cost of a College Degree: A Case Study of a SUNY Community College [PDF]

open access: yes, 2010
Inspired by a Delta Cost Project White Paper, this study uses different measures of calculating the cost of a college degree at an up‐state community college in New York.
Losinger, Regina   +2 more
core   +1 more source

The benefits of multidisciplinary collaboration in the successful management of two complex feline cases

open access: yesAustralian Veterinary Journal, EarlyView.
Despite a frequent misconception that behavioural concerns are diagnoses of exclusion, medical conditions and behavioural disorders are frequently inter‐related. In human medicine, the ‘multidisciplinary team’ approach (MDTA) is considered the most efficacious way of managing patients with complex and chronic health conditions.
BE Bollaert, JM Ley, HE Zulch
wiley   +1 more source

Oral Health Care Services, Barriers and Enablers to Maintaining Good Oral Health in Motor Neurone Disease: A Scoping Review

open access: yesCommunity Dentistry and Oral Epidemiology, EarlyView.
ABSTRACT Objectives The objective of this scoping review was to map existing literature on oral health and related care in individuals with Motor Neurone Disease (MND). Specifically, the review aimed to identify barriers and facilitators to maintaining oral hygiene, summarise available clinical guidelines and patient‐facing resources, and examine how ...
Mariam A. Khokhar   +3 more
wiley   +1 more source

The Diagnostic Odyssey of a Biochemically Confirmed Case of ML II: The First Western Patient With LYSET Deficiency

open access: yesClinical Genetics, EarlyView.
We identify a female patient with a homozygous nonsense variant (p.Gln38Ter) in the LYSET gene. This is the first western report of a challenging case of an extensive diagnostic odyssey and demonstrates that the LYSET gene must be considered in the differential diagnosis when M6P‐labeled lysosomal enzymes are altered.
Fernanda Sperb‐Ludwig   +5 more
wiley   +1 more source

Smile Stories: Investigating Pediatric Dental Anomalies a Cross-Sectional Study

open access: yesJournal of Islamic International Medical College
Objective: Determination of the frequency and distribution of dental anomalies across different age groups and gender within the pediatric population. Study Design: Cross-sectional observational study.
Mehwash Kashif , Irum Munir Raja , Uzma Zareef , Amna Rehman , Sana Adeeba Islam , Nabeel Khan
doaj   +1 more source

Comprehensive Assessment of the KDM2B‐Associated Neurodevelopmental Disorder and the 12q24.31 Microdeletion Syndrome

open access: yesClinical Genetics, EarlyView.
We set out to characterize genotype–phenotype correlations in the recently delineated KDM2B‐associated neurodevelopmental disorder. We observe a highly penetrant CxxC domain‐related phenotype with distinct facial features supported by GestaltMatcher. In contrast, our findings point to variable expressivity and incomplete penetrance of loss‐of‐function ...
Amber S. E. van Oirsouw   +30 more
wiley   +1 more source

Molecular Basis and Clinical Spectrum of WNT10A‐Related Oligodontia

open access: yesClinical Genetics, EarlyView.
Cellular Mechanism behind WNT10A phenotypes. ABSTRACT WNT10A mutations, a major genetic determinant of dental agenesis and ectodermal dysplasia, exert profound effects on craniofacial development. Although classified as rare disorders, these mutations account for more than half of oligodontia cases, reflecting their critical role.
Perennes Elise   +5 more
wiley   +1 more source

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