Results 131 to 140 of about 7,575 (221)

Enamel hypoplasia or amelogenesis imperfecta - a restorative approach

or acquired disturbances may lead to the development of alterations on enamel structure, compromising tooth esthetics and function. This short communication aims to briefly discuss the possibility of employment of several treatment options either to ...
Rodrigo Borges Fonseca, Lourenço Correr Sobrinho, Alfredo Júlio Fernandes Neto, Adérito Soares da Mota, Carlos José Soares
core  

An autosomal recessive mutation in SCL24A4 causing enamel hypoplasia in Samoyed and its relationship to breed-wide genetic diversity. [PDF]

Canine Genet Epidemiol, 2017
Pedersen NC, Shope B, Liu H.
europepmc   +1 more source

Long-Term Sequelae of Primary Tooth Injuries on Permanent Successors: A Case Series. [PDF]

Cureus
Goswami M, Gupta A, Kumar G, Johnson RM, Sultan F, Rimshheanam R.   +5 more
europepmc   +1 more source

Pediatric Dental Management of a Patient With Infantile Osteopetrosis in Remission: A Clinical Case Report. [PDF]

Case Rep Dent
Cruz-Morera MA, Molina-Chaves K, Gomez-Fernandez A.   +2 more
europepmc   +1 more source

Oral Health in Children With Congenital Heart Diseases: A Comprehensive Narrative Review. [PDF]

Clin Med Insights Pediatr
Saleh W, Elhusseiny GA, Alharbi H.
europepmc   +1 more source

Interdisciplinary Study of the Clinical Phenotype of Patients with Fibrodysplasia Ossificans Progressiva (FOP) in Dental Practice: A Cross-Sectional Clinical-Statistical Analysis. [PDF]

J Clin Med
Danshina S, Sevbitov A, Kazumova A, Borisov V, Timoshin A, Kuznetsova M, Dorofeev A.   +6 more
europepmc   +1 more source

Etch-Bleach-Seal Technique in Managing Enamel Hypomineralization: A Case Report With Narrative Literature Review. [PDF]

Case Rep Dent
Gharavi M, Tavassoli-Hojjati S, Abdolahpour Z.   +2 more
europepmc   +1 more source

Oral Health in Early and Advanced Stages (1-4) of Chronic Kidney Disease: A Systematic Review and Meta-Analysis. [PDF]

Int Dent J
Niederau C, Ali AA, Chahboun S, Kalim S, Portillo MR, Kramann R, Schulze-Späte U, Wolfart S, Jankowski J, Wolf M, Craveiro RB.   +10 more
europepmc   +1 more source

Jalili syndrome: Sibling cases with variable phenotypes. [PDF]

Indian J Ophthalmol
Sharda S, Bharti N.
europepmc   +1 more source

Axenfeld-Rieger Syndrome with Negative Chromosomal Microarray and Whole-Exome Sequencing: A Case Report. [PDF]

Int Med Case Rep J
Moraes PC, Montalli VAM, Sperandio M, Dos Santos AM, Rosa ACG.   +4 more
europepmc   +1 more source