Results 51 to 60 of about 4,008 (210)

Dental Stigmata and Skeletal Lesions of Congenital Treponematosis in Early Agricultural Vietnam (4000–3500 bp)

open access: yesInternational Journal of Osteoarchaeology, Volume 36, Issue 2, Page 401-413, March/April 2026.
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]

open access: yes, 2015
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

open access: yesJournal of Esthetic and Restorative Dentistry, Volume 38, Issue 3, Page 520-529, March 2026.
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

Co‐Occurrence of Osteogenesis Imperfecta Type III and Chronic Abruption‐Oligohydramnios Sequence: A Case Report Suggesting a Possible Role of Type I Collagen Fragility

open access: yesJournal of Obstetrics and Gynaecology Research, Volume 52, Issue 2, February 2026.
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]

open access: yes, 2011
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]

open access: yes, 2017
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

open access: yesJournal of Dentistry Indonesia, 2015
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

Prevalence, Characteristics, and Predictive Factors of Dentoalveolar and Spreading Odontogenic Infections in Children Treated Under General Anaesthesia

open access: yesInternational Journal of Paediatric Dentistry, Volume 36, Issue 1, Page 13-18, January 2026.
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]

open access: yes, 2016
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

Epidemiological and Clinical Features of Regional Odontodysplasia in South Korean Pediatric Patients: A Multicenter Case Series Study

open access: yesInternational Journal of Paediatric Dentistry, Volume 36, Issue 1, Page 140-152, January 2026.
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

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