Disease: Amelogenesis imperfecta
- <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 ODAPH mutation causing amelogenesis imperfecta and its expression in human dental tissues
- A pilot study comparing optical coherence tomography, radiography, clinical photography, and polarisation microscopy for studies of hypomineralisation disturbances in enamel
- A Review of Selected Dental Anomalies With Histologic Features in the Pediatric Patient
- Abnormal teeth and renal calcifications: Answers
- Abnormal teeth and renal calcifications: Questions
- AI-assisted dental care
- Amelogenesis imperfecta: More than just an enamel problem
- Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop's classification
- Amelogenesis imperfecta. case report
- 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
- 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, radiological, and genetic characterization of <em>SLC13A5</em> variants in Saudi families: Genotype phenotype correlation and brief review of the literature
- 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
- Deciphering the functions of Stromal Interaction Molecule-1 in amelogenesis using AmelX-iCre mice
- 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
- 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
- Developmental Disturbances of the Teeth, Anomalies of Structure
- Digenic inheritance accounts for phenotypic variability in amelogenesis imperfecta
- Digital restorative workflows for developmental dental defects in young patients: A case series
- 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
- Esthetic Rehabilitation of Pediatric Patients Using Direct Bonding Technique-A Case Series Report
- Etiology, Classification, and Restorative Management of Amelogenesis Imperfecta Among Children and Young Adults: A Scoping Review
- FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome
- FAM20A-Associated Amelogenesis Imperfecta: Gene Variants with Functional Verification and Histological Features
- Fam83h mutation causes mandible underdevelopment via CK1α-mediated Wnt/β-catenin signaling in male C57/BL6J mice
- Gingival proteomics reveals the role of TGF beta and YAP/TAZ signaling in Raine syndrome fibrosis
- 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
- 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
- Management of oral manifestations of a child with Heimler Syndrome-2
- MEMO1 Is Required for Ameloblast Maturation and Functional Enamel Formation
- Mesoscale structural gradients in human tooth enamel
- microRNA-382 as a tumor suppressor? Roles in tumorigenesis and clinical significance
- Misdiagnosed metabolic bone abnormality: a case report
- Molecular-based phenotype variations in amelogenesis imperfecta
- 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
- Non-syndromic generalised hypotaurodontism in a case of Stage III Grade C periodontitis
- Novel <em>WDR72</em> Mutations Causing Hypomaturation Amelogenesis Imperfecta
- Novel Ameloblastin Variants, Contrasting Amelogenesis Imperfecta Phenotypes
- Novel ITGB6 variants cause hypoplastic-hypomineralized amelogenesis imperfecta and taurodontism: characterization of tooth phenotype and review of literature
- Novel WDR72 Mutations Causing Hypomaturation Amelogenesis Imperfecta
- Ophthalmic Manifestations of Heimler Syndrome in Two Siblings With <em>PEX1</em> Variants
- Oro-dental phenotyping and report of three families with RELT-associated amelogenesis imperfecta
- Orofacial Anomalies in Kindler Epidermolysis Bullosa
- 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
- 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
- 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"
- Restaurative und rekonstruktive Behandlung einer Amelogenesis imperfecta nach 18 Jahren – ein publizierter Fall wird volljährig
- Role of Dental Professionals in the Management of a Dentigerous Cyst in a Patient With Amelogenesis Imperfecta
- 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
- Ultra-Widefield Imaging of Retinal Flecks and Corresponding Subretinal Hyperreflective Deposits in Heimler Syndrome
- Zellweger syndrome caused by PEX6 gene variation in 2 cases and literature review