Results 51 to 60 of about 2,625 (171)
FAM83H Regulates Postnatal T Cell Development Through Thymic Stroma Organization
European Journal of Immunology, Volume 56, Issue 1, January 2026.Loss of the casein kinase 1 scaffolding protein FAM83H compromises bone marrow lymphopoiesis, reduces Foxn1 expression in cortical thymic epithelial cells (TEC), disrupts thymic architecture and TEC identity, and ultimately impairs double‐negative thymocyte proliferation and T‐cell production.
Betul Melike Ogan +16 more
wiley +1 more source
Amelogenesis imperfecta with gingival calcification: a rare presentation
Brazilian Journal of Oral Sciences, 2015 The purpose of this article is to highlight the rare presence of gingival calcification with Amelogenesis Imperfecta. A case is presented of a 12-year-old girl with a defect of enamel in deciduous as well as permanent dentition with moderate amount of ...
Sunitha Carnelio, Nirmala Rao
doaj +1 more source
Restorative treatment in a case of amelogenesis imperfecta and 9-year follow-up: a case report
Head & Face Medicine, 2020 Background Amelogenesis imperfecta is a hereditary malformation showing various manifestations regarding enamel dysplasia. This case report shows a 9-year follow-up after restorative treatment of a 16-year old female patient affected by a hypoplastic ...
Martin M. I. Sabandal +2 more
doaj +1 more source
CDG due to Defective Membrane Transporters: Update
Journal of Inherited Metabolic Disease, Volume 49, Issue 1, January 2026.ABSTRACT Congenital disorders of glycosylation are genetic defects in the glycoprotein and glycolipid glycan assembly and attachment. Some 200 CDG have been reported since the first clinical description in 1980. Most CDG are enzymatic deficiencies, but 13 (6.5%) are defects in the ER, Golgi apparatus (GA), and plasma membrane transporters.
D. Quelhas, C. R. Ferreira, J. Jaeken
wiley +1 more source
International 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
International 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
Revista de la Asociación Odontológica Argentina, 2012 sumen Objetivo. Describir el manejo clínico para la restauración estética y funcional de un caso con amelogénesis imperfecta. Caso clínico. Paciente femenina de 15 años que presentaba alteración en la apariencia estética de sus dientes y episodios ...
Weider de Oliveira +5 more
doaj
Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta
Frontiers in Physiology, 2017 Amelogenesis imperfecta is a group of rare inherited disorders that affect tooth enamel formation, quantitatively and/or qualitatively. The aim of this study was to identify the genetic etiologies of two families presenting with hypomaturation ...
Jung-Wook Kim +11 more
doaj +1 more source
Cumhuriyet Dental Journal, 2014 Amelogenesis imperfecta (AI) encompasses a complicated group of hereditary conditions that cause developmental alterations in the structure of the enamel in the absence of a systemic disorder.
Derya Özdemir Doğan +2 more
doaj +1 more source