• A homozygous SP7/OSX mutation causes osteogenesis and dentinogenesis imperfecta with craniofacial anomalies
• A novel approach to full-mouth rehabilitation of dentinogenesis imperfecta type II: Case series with review of literature
• A novel compound heterozygous variation in the <em>FKBP10</em> gene causes Bruck syndrome without congenital contractures: A case report
• A novel DSPP frameshift mutation causing dentin dysplasia type 2 and disease management strategies
• A Novel Mutation in the <em>TRIP11</em> Gene: Diagnostic Approach from Relatively Common Skeletal Dysplasias to an Extremely Rare Odontochondrodysplasia
• A Review of Dentinogenesis Imperfecta and Primary Dentin Disorders in Dogs
• A Review of Selected Dental Anomalies With Histologic Features in the Pediatric Patient
• A standard set of outcome measures for the comprehensive assessment of oral health and occlusion in individuals with osteogenesis imperfecta
• AAV6-Mediated Gene Therapy Prevents Developmental Dentin Defects in a Dentinogenesis Imperfecta Type Ⅲ Mouse Model
• AAV6-Mediated Gene Therapy Prevents Developmental Dentin Defects in a Dentinogenesis Imperfecta Type Mouse Model
• An Aesthetic and Economic Approach of Smile Designing for a Patient With Dentinogenesis Imperfecta: A Rare Case Entity
• Analysis of the clinical and genetic characteristics of a Chinese family with osteogenesis imperfecta type I
• Chapter 4: Development Defects of Enamel and Dentine and Coronal Caries
• Characterization of three adults and an adolescent with Osteogenesis Imperfecta type VI and a novel founder SERPINF1 variant
• Clear Aligners in Patients with Amelogenesis and Dentinogenesis Imperfecta
• Clinical and genetic analysis of a pedigree affected with hereditary dentinogenesis imperfecta type II
• Clinical and Molecular Update on the Fourth Reported Family with Hamamy Syndrome
• Clinical Manifestations and Medical Imaging of Osteogenesis Imperfecta: Fetal Through Adulthood
• COL1A1 novel splice variant in osteogenesis imperfecta and splicing variants review: A case report
• Combination of osteogenesis imperfecta and hypophosphatasia in three children with multiple fractures, low bone mass and severe osteomalacia, a challenge for therapeutic management
• Combined exome sequencing and deep phenotyping in highly selected fetuses with skeletal dysplasia during the first and second trimesters improves diagnostic yield
• Comment reconnaître et distinguer les anomalies de structure dentaire ?
• Comprehensive Preventive and Therapeutic Oral Health Care: A Case Report of Mucopolysaccharidosis Type IV A in a Pediatric Patient
• Craniofacial and dental phenotype of two girls with osteogenesis imperfecta due to mutations in CRTAP
• Dental Abnormalities in Two Dental-Skeletal-Retinal Anomaly-Positive Cane Corso Dogs: A Case Series
• Dental Anomalies in a Sample of Lebanese Children: a Retrospective Study
• Dental anomalies in individuals with osteogenesis imperfecta: a systematic review and meta-analysis of prevalence and comparative studies
• Dental tissue changes in juvenile and adult mice with osteogenesis imperfecta
• Dentin defects caused by a Dspp^-1 frameshift mutation are associated with the activation of autophagy
• Dentinogenesis Imperfecta in a 1-Year-Old Female Labrador Retriever Dog: A Case Report and Literature Review
• Dentinogenesis imperfecta type 2: a case report
• Dentinogenesis imperfecta type II: Diagnosis, functional and esthetic rehabilitation in mixed dentition
• Dentinogenesis imperfecta: case report with nanoceramic resin crowns restorative treatment
• Developmental Disturbances of the Teeth, Anomalies of Structure
• Developmental Disturbances of the Teeth, Anomalies of Structure
• Differential lncRNA/mRNA Expression Profiling and Functional Network Analyses in Bmp2 Deletion of Mouse Dental Papilla Cells
• Discrepancies in the Phenotypical Classification of Osteogenesis Imperfecta in a Patient with COL1A2 Mutation: A Case Report
• DSPP dosage affects tooth development and dentin mineralization
• Dysregulation of MicroRNAs in Adult Osteogenesis Imperfecta: The miROI Study
• Effects of <em>DSPP</em> Gene Mutations on Periodontal Tissues
• Enamel Defects Associated With Dentin Sialophosphoprotein Mutation in Mice
• Establishment of a clinical network for children with amelogenesis imperfecta and dentinogenesis imperfecta in the UK: 4-year experience
• Evaluating the Prevalence and Distribution of Dental Anomalies in the Permanent Dentition of Patients Seeking Dental Care
• Extra-Skeletal Manifestations in Osteogenesis Imperfecta Mouse Models
• FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome
• Genotype-Phenotype Relationship and Follow-up Analysis of a Chinese Cohort With Osteogenesis Imperfecta
• Hereditary dentin defects with systemic diseases
• High bone mass phenotype in a cohort of patients with Osteogenesis Imperfecta caused due to <em>BMP1</em> and C-propeptide cleavage variants in <em>COL1A1</em>
• High bone mass phenotype in a cohort of patients with Osteogenesis Imperfecta caused due to BMP1 and C-propeptide cleavage variants in COL1A1
• Identification of DSPP novel variants and phenotype analysis in dentinogenesis dysplasia Shields type II patients
• Interdisciplinary Management of a Patient with Dentinogenesis Imperfecta Type II Using a Combination of CAD-CAM and Analog Techniques: A Clinical Report
• Intracranial aneurysm as a possible complication of osteogenesis imperfecta: a case series and literature review
• Isolated dentinogenesis imperfecta: Novel DSPP variants and insights on genetic counselling
• Long-term follow-up of severe autosomal recessive SP7-related bone disorder
• Loss of Bmp2 impairs odontogenesis via dysregulating pAkt/pErk/GCN5/Dlx3/Sp7
• Metaphyseal and posterior rib fractures in osteogenesis imperfecta: Case report and review of the literature
• Micro-CT study on isolated teeth with hereditary dentin defects
• Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and Their Genotype-phenotype Correlation
• Morphological and Ultrastructural Collagen Defects: Impact and Implications in Dentinogenesis Imperfecta
• Morphological Study of Dental Structure in Dentinogenesis Imperfecta Type I with Scanning Electron Microscopy
• Mouse Dspp frameshift model of human dentinogenesis imperfecta
• Mutation of dentin sialophosphoprotein and hereditary malformations of dentin
• Nanoscopic wear behavior of dentinogenesis imperfecta type II tooth dentin
• Non-Syndromic Dentinogenesis Imperfecta Caused by Mild Mutations in <em>COL1A2</em>
• Non-Syndromic Dentinogenesis Imperfecta Caused by Mild Mutations in COL1A2
• Novel dentin sialophosphoprotein gene frameshift mutations affect dentin mineralization
• Novel pathogenic variants in SPARC as cause of osteogenesis imperfecta: Two case reports
• Optimising Health-Related Quality of Life in Children With Osteogenesis Imperfecta
• Oral health-related quality of life in children with osteogenesis imperfecta
• Orthodontic treatment of a patient with dentinogenesis imperfecta using a clear aligner system
• Osteogenesis Imperfecta
• Osteogenesis Imperfecta
• Osteogenesis Imperfecta Diagnosed in an Active Duty Female Due to CREB3L1 Heterozygosity
• Osteogenesis imperfecta type III: Oral, craniofacial characteristics and atypical radiographic findings oral
• Pamidronate Therapy Increases Trabecular Bone Complexity of Mandibular Condyles in Individuals with Osteogenesis Imperfecta
• Pattern and prevalence of dental anomalies among a paediatric population in Lagos, Nigeria
• Phenotype and molecular characterizations of a family with dentinogenesis imperfecta shields type II with a novel <em>DSPP</em> mutation
• Phenotype and molecular characterizations of a family with dentinogenesis imperfecta shields type II with a novel DSPP mutation
• Pretreatments to bonding on enamel and dentin disorders: a systematic review
• Prevalence and Distribution of Selected Dental Anomalies in the Patients Reporting to Dental Institute, RIMS, Ranchi
• Progress in the classification of hereditary dentin disorders and clinical management strategies
• Recognition on dentin dysplasia type Ⅱ
• Regenerative Endodontic Procedures in Immature Teeth Affected by Regional Odontodysplasia
• Regenerative Endodontic Treatment in Dentinogenesis Imperfecta-Induced Apical Periodontitis
• Skeletal and Non-skeletal Phenotypes in Children with Osteogenesis Imperfecta
• Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand abnormal calcification type: Further expanding the mutational spectrum and dental findings of three new patients
• Systematic review of health related-quality of life in adults with osteogenesis imperfecta
• The First Compound Heterozygous Mutations of DMP1 Causing Rare Autosomal Recessive Hypophosphatemic Rickets Type 1
• The impact of craniofacial and dental osteogenesis imperfecta manifestations on oral health-related quality of life of children and adolescents
• The Modified Shields Classification and 12 Families with Defined <em>DSPP</em> Mutations
• The paediatric dentistry-restorative dentistry interface
• The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry
• The role of Dentin Sialophosphoprotein (DSPP) in craniofacial development
• The Role of DSPP in Dentine Formation and Hereditary Dentine Defects
• Tibial plateau fracture and RNA sequencing with osteogenesis imperfecta: a case report
• Translated Mutant <em>DSPP</em> mRNA Expression Level Impacts the Severity of Dentin Defects
• Unequal Impact of <em>COL1A1</em> and <em>COL1A2</em> Variants on Dentinogenesis Imperfecta
• Unequal Impact of COL1A1 and COL1A2 Variants on Dentinogenesis Imperfecta
• Withdrawal: A novel DSPP frameshift mutation causing dentin dysplasia type 2 and disease management strategies
• Z-osteotomy for uniplanar femoral shaft deformity correction in an adolescent with osteogenesis imperfecta