Results 181 to 190 of about 5,447 (248)
Abstract Objective The aim of this systematic review and meta‐analysis was to evaluate the longitudinal temporal pattern of periodontal probing depth (PPD) reduction in intrabony periodontal defects following non‐surgical periodontal therapy (NSPT), both as a monotherapy and with adjunctive locally delivered pharmacological agents.
Luca Ramaglia +4 more
wiley +1 more source
Micro-Raman Spectroscopy Reveals Compositional Alterations in Molar Incisor Hypomineralization and Enamel Adjacent to Demarcated Opacities. [PDF]
Rexhaj F, Shah FA, Lundgren T.
europepmc +1 more source
Abstract Objectives This review synthesizes evidence regarding the prevalence, epidemiological associations, and mechanistic pathways between osteoporosis, periodontal disease, and dental implant therapy. Materials and Methods A literature review was conducted to identify studies focused on: osteoporosis, periodontal disease, and dental implants ...
Samin Sirous +4 more
wiley +1 more source
Metabolic programming in tooth development: a regulatory network from energy substrates to signaling instructions. [PDF]
Cao X, Gao Y, Liu W, Sun X.
europepmc +1 more source
Abstract Objectives To evaluate the clinical and radiographic efficacy of the adjunctive use of hyaluronic acid (HA) in regenerative periodontal surgery for the treatment of intrabony defects. Materials and Methods A systematic search identified randomized controlled trials (RCTs) involving adult patients with intrabony defects who underwent ...
Abdusalam E. Alrmali +6 more
wiley +1 more source
Prevalence, clinical characteristics, and dental complaints of molar incisor hypomineralization among Saudi children in Abha: a hospital-based survey. [PDF]
M Mustafa M, Mohamed N, M Nurelhuda N.
europepmc +1 more source
Monoallelic POLR3A Variants Cause Early‐Onset Peripheral Neuropathy
Objective Biallelic variants in genes encoding the RNA polymerase III complex (Pol III) cause a spectrum of neurological disorders primarily affecting the central nervous system. Monoallelic variants have been reported in the POLR3B subunit only, associated with neurodevelopmental disorder, epilepsy, and peripheral neuropathy.
Luiza L. P. Ramos +46 more
wiley +1 more source
Multidisciplinary Oral Rehabilitation in Osteogenesis Imperfecta: 18‐Year‐Old Case Report
ABSTRACT Osteogenesis imperfecta (OI) is a hereditary connective tissue disorder characterized by bone fragility and Type I collagen defects. Although dentinogenesis imperfecta (DI) is a classic manifestation, patients with OI may experience significant dental deterioration even in its absence due to inherent dentinal weakness.
Pegah Mosannen Mozafari +3 more
wiley +1 more source
Long-Term Sequelae of Primary Tooth Injuries on Permanent Successors: A Case Series. [PDF]
Goswami M +5 more
europepmc +1 more source

