• <em>Amelogenesis imperfecta</em>: Next-generation sequencing sheds light on Witkop's classification
• <em>In vivo</em> real-time assessment of developmental defects in enamel of anti-Act1 mice using optical coherence tomography
• A 25-Year Retro-prospective Study on Prosthetic Rehabilitation with Bonded Ceramics of Patients with Amelogenesis Imperfecta
• A novel <em>ODAPH</em> mutation causing amelogenesis imperfecta and its expression in human dental tissues
• A novel mutation in GPR68 causes hypomaturation amelogenesis imperfecta
• A novel ODAPH mutation causing amelogenesis imperfecta and its expression in human dental tissues
• A Review of Selected Dental Anomalies With Histologic Features in the Pediatric Patient
• Advances in clinical diagnosis and management of amelogenesis imperfecta in children and adolescents
• Ameloblastin and its multifunctionality in amelogenesis: A review
• Amelogenesis imperfecta: More than just an enamel problem
• Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop's classification
• Amelogenesis imperfecta. case report
• AMELX Mutations and Genotype-Phenotype Correlation in X-Linked Amelogenesis Imperfecta
• Analysis of amelogenesis imperfecta with abnormal tooth eruption caused by FAM83H mutation
• Analysis of phenotype and pathogenic variant in a case of Heimler syndrome
• Association between malocclusions and amelogenesis imperfecta genotype and phenotype: A systematic review
• Authors' reply to: Deep dental phenotyping and a novel FAM20A variant in patients with amelogenesis imperfecta type IG
• Autoimmune amelogenesis imperfecta in patients with APS-1 and coeliac disease
• Autophagy Plays a Crucial Role in Ameloblast Differentiation
• Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability
• Brachyolmia, dental anomalies and short stature (DASS): Phenotype and genotype analyses of Egyptian and Pakistani patients
• Carbonic anhydrase II deficiency syndrome with amelogenesis imperfecta linked to a homozygous <em>CA2</em> deletion
• Carbonic anhydrase II deficiency syndrome with amelogenesis imperfecta linked to a homozygous CA2 deletion
• Case report: Enamel renal syndrome: a case series from sub-Saharan Africa
• Chapter 4: Development Defects of Enamel and Dentine and Coronal Caries
• Clinical characteristics and genetic profile of children with WDR72-associated distal renal tubular acidosis: a nationwide experience
• Comment on: Deep dental phenotyping and a novel FAM20A variant in patients with amelogenesis imperfecta type IG
• Comment reconnaître et distinguer les anomalies de structure dentaire ?
• Craniofacial Cephalometric Characteristics and Open Bite Deformity in Individuals with Amelogenesis Imperfecta-A Systematic Review and Meta-Analysis
• CRISPR/Cas9-Induced Fam83h Knock-out Leads to Impaired Wnt/β-Catenin Pathway and Altered Expression of Tooth Mineralization Genes in Mice
• Crucial Role of microRNAs as New Targets for Amelogenesis Disorders Detection
• Deep dental phenotyping and a novel FAM20A variant in patients with amelogenesis imperfecta type IG
• Deep dental phenotyping and a novel FAM20A variant in patients with amelogenesis imperfecta type IG
• Dental and jawbone abnormalities linked to amelogenesis imperfecta: A retrospective and analytic study comparing panoramic radiographs
• Dental Anomalies in a Sample of Lebanese Children: a Retrospective Study
• Dental treatment approaches of amelogenesis imperfecta in children and young adults: A systematic review of the literature
• Dentofacial manifestations in a child with Jalili syndrome
• Developmental Defects of Enamel: A Bibliometric Analysis of the Top 100 Most-Cited Papers
• Developmental Disturbances of the Teeth, Anomalies of Structure
• Digenic inheritance accounts for phenotypic variability in amelogenesis imperfecta
• ENAM Mutations Can Cause Hypomaturation Amelogenesis Imperfecta
• Enamel Renal Gingival Syndrome in an Adolescent
• Enamel renal syndrome: A case report with calcifications in pulp, gingivae, dental follicle and kidneys
• Epileptic encephalopathy and amelogenesis imperfecta: What about KohlschuttereTonz syndrome? Case report and literature review
• Establishment of a clinical network for children with amelogenesis imperfecta and dentinogenesis imperfecta in the UK: 4-year experience
• Etiology, Classification, and Restorative Management of Amelogenesis Imperfecta Among Children and Young Adults: A Scoping Review
• Evaluation of <em>Ilex guayusa</em> and <em>Piper marginatum</em> Extract Cytotoxicity on Human Dental Pulp Mesenchymal Stem Cells
• FAM20A-Associated Amelogenesis Imperfecta: Gene Variants with Functional Verification and Histological Features
• Full-Mouth Rehabilitation of a 15-Year-Old Girl Affected by a Rare Hypoparathyroidism (Glial Cell Missing Homolog 2 Mutation): A 3-Year Follow-Up
• Gingival proteomics reveals the role of TGF beta and YAP/TAZ signaling in Raine syndrome fibrosis
• Heimler syndrome with a complaint of blurred vision caused by compound heterozygous variants in <em>PEX1</em>
• Heterozygous <em>COL17A1</em> variants are a frequent cause of amelogenesis imperfecta
• Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta
• How to optimize bonding procedures on healthy and hypomineralized enamel in orthodontics?
• Identification of a Novel Homozygous Missense Mutation in the CLDN16 Gene to Decipher the Ambiguous Clinical Presentation Associated with Autosomal Dominant Hypocalcaemia and Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis in an Indian Fa
• IDENTIFICATION OF A NOVEL LTBP3 GENE PATHOGENIC VARIANT IN DRUZE ARAB PATIENTS PRESENTED WITH SYNDROMIC SHORT STATURE WITH BRACHYOLMIA AND AMELOGENESIS IMPERFECTA
• Identification of novel homozygous nonsense SLC10A7 variant causing short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis and surgical management of spine
• In-depth investigation of FAM20A insufficiency effects on deciduous dental pulp cells: Altered behaviours, osteogenic differentiation, and inflammatory gene expression
• Insights into molar-incisor hypomineralisation in past populations: A call to anthropologists
• Interdisciplinary full mouth rehabilitation of a patient with amelogenesis imperfecta from childhood to young adult-hood: A 12-year case report
• Interdisciplinary rehabilitation using CAD-CAM technology for a young patient with severe malocclusion and amelogenesis imperfecta: A 5-year follow-up case report
• Internal Tooth Whitening
• Is Italian Dentists' Knowledge of Enamel Development Defects Adequate? A Nationwide Survey
• Kohlschutter-Tonz syndrome (amelo-cerebro-hypohidrotic syndrome) in an Indian family with a novel ROGD1 mutation
• LAMB3: Central role and clinical significance in neoplastic and non-neoplastic diseases
• Management of oral manifestations of a child with Heimler Syndrome-2
• MAST4 regulates stem cell maintenance with DLX3 for epithelial development and amelogenesis
• MEMO1 Is Required for Ameloblast Maturation and Functional Enamel Formation
• microRNA-382 as a tumor suppressor? Roles in tumorigenesis and clinical significance
• Mini-implant assisted palate expansion and digital design in junctional epidermolysis bullosa and amelogenesis imperfecta: Case report
• Misdiagnosed metabolic bone abnormality: a case report
• Mutations Causing X-Linked Amelogenesis Imperfecta Alter miRNA Formation from Amelogenin Exon4
• Navigating Complexity: A Case Report on a Comprehensive Dental Management Approach to Amelogenesis Imperfecta and Gingival Fibromatosis Syndrome
• Novel Ameloblastin Variants, Contrasting Amelogenesis Imperfecta Phenotypes
• Oro-dental phenotyping and report of three families with RELT-associated amelogenesis imperfecta
• Orofacial Anomalies in Kindler Epidermolysis Bullosa
• Orthodontic findings and treatment need in patients with amelogenesis imperfecta: a descriptive analysis
• Orthodontic management of amelogenesis imperfecta: A case report
• Overexpression of ameloblastin in secretory ameloblasts results in demarcated, hypomineralized opacities in enamel
• Pankey Mann Schuyler Philosophy-Based Prosthetic Rehabilitation for an Amelogenesis Imperfecta Patient: A Case Report
• Perampanel effectiveness in treating ROGDI-related Kohlschütter-Tönz syndrome: first reported case in China and literature review
• Pretreatments to bonding on enamel and dentin disorders: a systematic review
• Prevalence of Dental Anomalies Among Orthodontic Patients: A Retrospective Study in Saudi Arabia
• Prosthodontic rehabilitation of two siblings with hypoplastic (type 1) amelogenesis imperfecta: A case report
• Protocol for generating three-dimensional induced early ameloblasts using serum-free media and growth factors
• Recessive <em>COL17A1</em> Mutations and a Dominant <em>LAMB3</em> Mutation Cause Hypoplastic Amelogenesis Imperfecta
• Recessive COL17A1 Mutations and a Dominant LAMB3 Mutation Cause Hypoplastic Amelogenesis Imperfecta
• Regenerative Endodontic Procedures in Immature Teeth Affected by Regional Odontodysplasia
• Renal tubular estrogen ß receptors are expressed at high levels in small vessel vasculitis and are primarily localized in the distal tubule
• Response to Letter, "Autophagy Plays a Crucial Role in Ameloblast Differentiation"
• Roles of the histone methyltransferase SET domain bifurcated 1 in epithelial cells during tooth development
• Single-cell census of human tooth development enables generation of human enamel
• SOFT syndrome with kohlschutter-Tonz syndrome
• Splicing mutations in AMELX and ENAM cause amelogenesis imperfecta
• The Rogdi knockout mouse is a model for Kohlschütter-Tönz syndrome
• The rough-toothed dolphin genome provides new insights into the genetic mechanism of its rough teeth
• Tooth ultrastructure changes induced by a nonsense mutation in the FAM83H gene: insights into the diversity of amelogenesis imperfecta
• Total rehabilitation in case of amelogenesis imperfecta
• Unraveling neuroimaging insights in developmental epileptic encephalopathy type 25: a comprehensive review of reported cases and a novel SLC13A5 variant
• Zellweger syndrome caused by PEX6 gene variation in 2 cases and literature review