Results 241 to 250 of about 85,299 (314)

Self‐Determination in Action: A Scoping Review on Oral Health Training for Indigenous Health Workers Globally

open access: yesCommunity Dentistry and Oral Epidemiology, EarlyView.
ABSTRACT Globally, the systemic marginalisation of Indigenous Peoples has led to significant health disparities rooted in the legacy of colonisation and ongoing settler colonialism. Objective This scoping review aimed to collate oral health promotion training programmes tailored for Indigenous Health Workers (IHW), who play a pivotal role in improving ...
Madison Cachagee   +6 more
wiley   +1 more source

PIK3C2A‐Related Clinical Phenotype and Cellular Charaterization Linked to Functional SHH Primary Cilia Defect

open access: yesClinical Genetics, EarlyView.
Trio exome sequencing allowed the identification of two novel compound heterozygous variants in PIK3C2A, defining the fifth family presenting a PIK3C2A‐related syndrome characterized by pulverulent cataracts and deafness. Functional testing revealed impaired PI metabolism and primary dysfunction phenotype.
Adella Karam   +9 more
wiley   +1 more source

Preoperative Re-evaluation of Planned Orthognathic Surgical Procedures. [PDF]

open access: yesCureus
Mutoh M   +6 more
europepmc   +1 more source

Unraveling the Role of WDR91: Case Report of a Previously Unrecognized Clinical Entity

open access: yesClinical Genetics, EarlyView.
A novel case is herein described to expand the genetic and clinical spectrum of WDR91 and characterize a previously unrecognized autosomal recessive neurodevelopmental disorder. WDR91 deficiency results in neuronal loss, cortical thinning, and impaired brain development.
Nikolaos M. Marinakis   +14 more
wiley   +1 more source

Missense Variants in the Second Transmembrane Domain of TMEM17 Disrupt Its Stability and Function and Lead to a Wide Phenotypic Spectrum of Ciliopathies

open access: yesClinical Genetics, EarlyView.
Missense variants in TMEM17 disrupt its localization and function at the ciliary transition zone, leading to a wide range of ciliopathy phenotypes, from OFD6 and Joubert syndromes to Meckel syndrome. ABSTRACT Ciliopathies are rare genetic disorders characterized by significant genetic and phenotypic variability.
Lucile Boutaud   +19 more
wiley   +1 more source

Influence of Bone Density and Guide Protocol on the Accuracy of Self‐Cutting Implants Using Static Guided Implant Placement—An In Vitro Study

open access: yesClinical Oral Implants Research, EarlyView.
ABSTRACT Introduction To investigate the influence of bone density and guide protocol on the accuracy of static guided implant placement of self‐cutting implants in vitro. Methods A total of 242 implant replicas of self‐cutting implants and implants with a tapered design as a control were placed in 40 maxilla replica models with healed posterior ridges
Caroline Streichfuss   +2 more
wiley   +1 more source

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