Results 51 to 60 of about 4,008 (210)
ABSTRACT Prior research has documented treponematosis at a single site in Mainland Southeast Asia from northern Vietnam dated to the early agricultural transition (~4000–3500 bp). To date, no other cases in Southeast Asia's prehistory have been identified.
Melandri Vlok +15 more
wiley +1 more source
A secretory kinase complex regulates extracellular protein phosphorylation. [PDF]
Although numerous extracellular phosphoproteins have been identified, the protein kinases within the secretory pathway have only recently been discovered, and their regulation is virtually unexplored.
Cui, Jixin +5 more
core +2 more sources
Advances in 3D Printing for Removable Prosthetics—Insights and Perspectives
ABSTRACT Objective This review summarizes recent advances in three‐dimensional (3D) printing for removable prosthodontics, including complete dentures, removable partial dentures, implant‐retained overdentures, and occlusal splints. The aim is to provide clinicians with an overview of current technologies, clinical performance, and future perspectives.
O. Schubert +3 more
wiley +1 more source
ABSTRACT Pregnancy complicated by severe osteogenesis imperfecta (OI) is rare, and chronic abruption‐oligohydramnios sequence (CAOS) is an uncommon obstetric disorder characterized by persistent bleeding and oligohydramnios without membrane rupture. To our knowledge, this is the first report describing the coexistence of type III OI and CAOS. A 24‐year‐
Ayumi Okuyama +5 more
wiley +1 more source
An unusual presentation of osteogenesis imperfecta type I [PDF]
Marta Rebelo, Jandira Lima, José Diniz Vieira, José Nascimento CostaDepartment of Internal Medicine, University Hospital of Coimbra, Coimbra, PortugalAbstract: Osteogenesis imperfecta (OI) is a rare inherited disorder with a broad ...
Costa JN, Lima J, Rebelo M, Vieira JD
core +1 more source
Stomatološko liječenje kod osteogenesis imperfecta [PDF]
Osteogenesis imperfecta is a very rare heterogeneous genetic disorder associated with the development of connective tissue resulting in fragile bones and frequent fractures.
Hrvoje Brkić, Ivana Savić Pavičin
core +2 more sources
Genetic Aspects of Dentinogenesis Imperfecta
Dentinogenesis Imperfecta (DI) is a hereditary, simple autosomal dominant disorder showing abnormalities in the dentin of the developing teeth and occurring at a rate of about 1 in 8000 births.
Elza Ibrahim Auerkari, Hedijanti Joenoes
doaj +1 more source
ABSTRACT Background Children receiving dental treatment under general anesthesia (GA) often have odontogenic infections (OIs). Early detection and treatment of patients at risk of OIs can improve oral health and prevent early tooth extractions. Aim To investigate the prevalence, characteristics, and predictive factors of OIs in children receiving ...
Annmari Hyppänen +4 more
wiley +1 more source
Diagnostic conundrums in antenatal presentation of a skeletal dysplasia with description of a heterozygous C-propeptide mutation in COL1A1 associated with a severe presentation of osteogenesis imperfecta [PDF]
Prompt and accurate diagnosis of skeletal dysplasias can play a crucial role in ensuring appropriate counseling and management (both antenatal and postnatal).
Bonafe +10 more
core +1 more source
ABSTRACT Background Regional odontodysplasia (RO) is a rare developmental dental anomaly with unknown prevalence. Current knowledge is largely limited to individual case reports. Aim This study aims to present epidemiological data, clinical features, and radiographic characteristics of pediatric and adolescent patients with RO in South Korea. Design In
So Dam Lee +5 more
wiley +1 more source

