Results 51 to 60 of about 3,771 (192)

Amelogénesis imperfecta. Caso clínico. Tratamiento ortodóncico interceptivo Amelogenesis imperfecta. Clinical case. Interceptive orthodontic treatment

open access: yesRevista de la Asociación Odontológica Argentina, 2011
Resumen La amelogénesis imperfecta (AI) es una anomalía de origen genómico que altera en diferente grado la estructura del esmalte produciendo problemas de autoestima, deterioro de la salud bucal en general y la consecuente disminución de la calidad ...
María Tenenbaum Batkis   +2 more
doaj  

Identification of novel homozygous nonsense SLC10A7 variant causing short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis and surgical management of spine

open access: yesOrphanet Journal of Rare Diseases, 2023
Background Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis is a rare, autosomal recessive, skeletal disorder first described in 2018.
Wenyan Zhang   +6 more
doaj   +1 more source

Distribution and Clinical Characteristics of MIH in Schoolchildren From the Central Peruvian Jungle: A Cross‑Sectional Study

open access: yesInternational Journal of Dentistry, Volume 2026, Issue 1, 2026.
Background Molar incisor hypomineralisation (MIH) is a developmental enamel defect that predominantly affects first permanent molars and frequently involves incisors. However, evidence on MIH prevalence and clinical presentation in jungle regions is limited.
Mayra Belen Barahona-Hernandez   +6 more
wiley   +1 more source

Palateless Maxillary Implant‐Supported Overdentures: A Review of Patient Satisfaction and Clinical Outcomes Along With Case Series

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Implant‐supported overdenture is a lifesaver treatment plan for edentulous patients. Implant numbers and positions in the maxilla and mandible are controversial, but in more studies on a minimum number of implants, which is at least four implants in the maxilla and two implants in the mandible, there is a consensus. Also, the attachment system
Zahra Jandaghian, Somayeh Zeighami
wiley   +1 more source

Amelogenesis imperfecta with gingival calcification: a rare presentation

open access: yesBrazilian 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

DIRECT RECONSTRUCTION OF PERMANENT DENTITION OF A PATIENT WITH AMELOGENESIS IMPERFECTA

open access: yesČeská Stomatologie a Praktické Zubní Lékařství, 2020
Introduction and aim: Amelogenesis imperfecta associates a clinically and genetically heterogeneous group of developmental defects affecting the appearance and structure of enamel, which more or less severely affect all dental functions.
T Kovalský   +3 more
doaj   +1 more source

AI in Root Canal Morphology: A Detailed Bibliometric Analysis of Research Trends and Global Contributions

open access: yesClinical and Experimental Dental Research, Volume 11, Issue 6, December 2025.
ABSTRACT Background Artificial Intelligence (AI) has emerged as a transformative tool in various scientific disciplines. Objective The study aims to provide a comprehensive bibliometric analysis of the literature on AI and root canal morphology, examining publication trends, author contributions, and thematic focus areas.
Waseem Hassan   +3 more
wiley   +1 more source

Full‐mouth rehabilitation choices depending on amelogenesis imperfecta's type: A familial case report

open access: yesClinical Case Reports, 2022
Amelogenesis imperfecta, a rare disease, represents inherited, congenital defects that primarily affect enamel with esthetic and functional impairment affecting everyday life.
Salomé Mascarell   +3 more
doaj   +1 more source

Mineralizing Elastin‐Like Protein Microgels

open access: yesJournal of Biomedical Materials Research Part A, Volume 113, Issue 12, December 2025.
ABSTRACT Mineralized tissues, such as bone and enamel are fundamental to the structure and function of organisms, with a complex interplay between their organic and inorganic components. Organized mineralization is crucial for both the tissues of living organisms and engineered materials.
Ieva Sapjanskaite   +7 more
wiley   +1 more source

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

open access: yesClinical Genetics, Volume 108, Issue 6, Page 696-707, December 2025.
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

Home - About - Disclaimer - Privacy