• 'BLUES' procedure for assessing the blue level of the sclera in Osteogenesis Imperfecta
• A case of osteogenesis imperfecta diagnosed after subchondral insufficiency fracture of bilateral femoral heads
• A Dyadic Nosology for Osteogenesis Imperfecta and Bone Fragility Syndromes 2024
• A recurrent de novo missense mutation in COL1A1 causes osteogenesis imperfecta type II and preterm delivery in Normande cattle
• A Retrospective Study of the Presentation, Diagnosis, Management, and Outcomes of 27 Patients with Osteogenesis Imperfecta at a Single Center in Turkiye
• A standard set of outcome measures for the comprehensive assessment of oral health and occlusion in individuals with osteogenesis imperfecta
• A Transoral Approach to Decompression Odontoidectomy With Posterior Wiring and Fusion for Pediatric Platybasia With Chiari Malformation
• Active Euthanasia for Perinatal Osteogenesis Imperfecta; An Ethical Dilemma in a Tertiary Facility in Southwestern Nigeria: A Case Report
• Alendronate treatment rescues the effects of compressive loading of TMJ in osteogenesis imperfecta mice
• An exploratory open-label multicentre phase I/II trial evaluating the safety and efficacy of postnatal or prenatal and postnatal administration of allogeneic expanded fetal mesenchymal stem cells for the treatment of severe osteogenesis imperfecta in infa
• Analyses of Osteogenesis Imperfecta in South Korea Using the Nationwide Health Insurance Service Claim Data: A Propensity Score-Matched Study
• Beneficial effects of romosozumab on bone mineral density and trabecular bone score assessed by dual-energy X-ray absorptiometry in a family with osteogenesis imperfecta
• Bioethical challenges in postwar development aid: The Rwandan case study
• Bone matrix properties in adults with osteogenesis imperfecta are not adversely affected by Setrusumab - a sclerostin neutralizing antibody
• Caregiver Burden, Parenting Stress and Coping Strategies: The Experience of Parents of Children and Adolescents with Osteogenesis Imperfecta
• Changes in serum bone turnover markers and bone mineral density Z-score in children with osteogenesis imperfecta after zoledronic acid treatment
• Characterization of hearing loss in pediatric patients with osteogenesis imperfecta
• Clinical spectrum of rare bone fragility disorders and response to bisphosphonate treatment: a retrospective study
• Clinical utility of comprehensive gene panel testing for common and rare causes of skeletal dysplasia and other skeletal disorders: Results from the largest cohort to date
• Collagen mutation and age contribute to differential craniofacial phenotypes in mouse models of osteogenesis imperfecta
• Combining anabolic loading and raloxifene improves bone quantity and some quality measures in a mouse model of osteogenesis imperfecta
• Congenital Contractures and Fractures: A Variant of Bruck Syndrome Type 2
• Correction to "Analysis of the clinical and genetic characteristics of a Chinese family with osteogenesis imperfecta type I"
• Correlation of serum DKK1 level with skeletal phenotype in children with osteogenesis imperfecta
• Craniofacial dysmorphism of osteogenesis imperfecta mouse and effect of cathepsin K knockout: Preliminary craniometry observations
• Cross-sectional and longitudinal analysis of bone age maturation during peri-pubertal growth in children with type I, III and IV osteogenesis imperfecta
• Current situation of osteogenesis imperfecta in Spain: results from a Delphi study
• Data collection on rare bone and mineral conditions in Europe: The landscape of registries and databases
• Dental Profile of Brazilian Patients with Rare Skeletal Genetic Disorders: Clinical Features and Associated Factors
• Dickkopf-1 (DKK1) blockade mitigates osteogenesis imperfecta (OI) related bone disease
• Disruption of the creb3l1 gene causes defects in caudal fin regeneration and patterning in zebrafish Danio rerio
• Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta
• Efficacy of intraoperative use of tranexamic acid in reducing blood loss from telescoping nail application in osteogenesis imperfecta. A randomized controlled trial
• Evaluation of the Nordic Musculoskeletal Questionnaire for Measuring Prevalence and the Consequence of Pain in a Danish Adult OI Population: A Pilot Study
• Exome Sequencing for the Diagnostics of Osteogenesis Imperfecta in Six Russian Patients
• Exploring the Implications of Golgi Apparatus Dysfunction in Bone Diseases
• Extra-Skeletal Manifestations in Osteogenesis Imperfecta Mouse Models
• From bone to nanoparticles: development of a novel generation of bone derived nanoparticles for image guided orthopedic regeneration
• Galunisertib downregulates mutant type I collagen expression and promotes MSCs osteogenesis in pediatric osteogenesis imperfecta
• Generation of bone-specific lysyl hydroxylase 2 knockout mice and their phenotypes
• Genetic Anomalies in Pediatric Orthopedics: A Case Study of a New Rare Sporadic Mutation of Osteogenesis Imperfecta
• Genotype and Phenotype Correlation of Patients with Osteogenesis Imperfecta
• Gnathodiaphyseal dysplasia: Diagnostic clues from two fetal cases and literature review
• Iatrogenic Intraoperative Fracture in Patients With Osteogenesis Imperfecta
• IFITM5-related (type V) osteogenesis imperfecta with evidence of perinatal involvement: A case report
• In Utero Gene Therapy and its Application in Genetic Hearing Loss
• Jaccoud's arthropathy in osteogenesis imperfecta
• Jazz Musicians and Their Disabilities: Django Reinhardt, Les Paul, and Michel Petrucciani
• Letter to the Editor from Bala and Dayal: "Safety and Efficacy of Denosumab in Children With Osteogenesis Imperfecta - the First Prospective Comparative Study"
• Letter to the editor: Re: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification
• Loss of the long form of Plod2 phenocopies contractures of Bruck syndrome - osteogenesis imperfecta
• Low muscle density in children with osteogenesis imperfecta using opportunistic low-dose chest CT: a case-control study
• Lumbar Epidural versus Caudal Epidural for Postoperative Analgesia After Lower Extremity Osteotomy Surgery in Pediatric Patients with Osteogenesis Imperfecta: A Propensity-Matched Cohort Analysis in a Single-Center Over 9 Years
• Management of Combined Fracture Neck of Femur and Femoral Deformity in Osteogenesis Imperfecta Patient: A Case Report
• Midterm Outcomes of Multimodal Approach to Treating Severe Scoliosis in Patients With Osteogenesis Imperfecta
• Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and Their Genotype-phenotype Correlation
• Monoclonal antibody anti-sclerostin for treatment of pelvic insufficiency fractures in adult hypophosphatasia: A case report
• Multi-omics analyses reveal aberrant differentiation trajectory with WNT1 loss-of-function in type XV osteogenesis imperfecta
• Multidisciplinary Management of Pregnancy in Patients With Osteogenesis Imperfecta Type 3
• Musculoskeletal System and Gait Characteristics in Patients with Osteogenesis imperfecta
• National Trends in Inpatient Hospital Outcomes of Children with Osteogenesis Imperfecta and the Importance of Extra-skeletal Manifestations: A Kids' Inpatient Database Study
• National Trends in Inpatient Hospital Outcomes of Children with Osteogenesis Imperfecta and the Importance of Extraskeletal Manifestations: A Kids' Inpatient Database Study
• Nutritional Behavior of Patients with Bone Diseases: A Cross-Sectional Study from Austria
• Optimising Health-Related Quality of Life in Children With Osteogenesis Imperfecta
• Osteogenesis Imperfecta type 1: like mother, like daughter - Challenges in the perinatal management
• Osteogenesis imperfecta type 10 and the cellular scaffolds underlying common immunological diseases
• Osteogenesis Imperfecta Type II: The Lethal Newborn Form Diagnosed in the Postnatal Period
• Osteogenesis Imperfecta: Skeletal and Non-skeletal Challenges in Adulthood
• Osteoid osteoma appearing after bony fracture in a girl with osteogenesis imperfecta
• Pamidronate Response in a Novel Biallelic CREB3L1 Gene Mutation-Associated Osteogenesis Imperfecta: A Case Report
• Perioperative Evaluation and Management of Children with Osteoporosis and Low Bone Mineral Density
• Polarization-sensitive optical coherence tomography and scleral collagen fiber orientation in osteogenesis imperfecta
• Pregnancy complicated by severe osteogenesis imperfecta poses a challenge for the anaesthetist: A case report
• Pregnancy complications and birth outcome in patients with osteogenesis imperfecta - A population-based register study
• Presentation of Rare Phenotypes Associated with the <em>FKBP10</em> Gene
• Pretreatments to bonding on enamel and dentin disorders: a systematic review
• Prevalence, number of fractures, and hospital characteristics among the pediatric population with osteogenesis imperfecta: results from the nationwide registry of Turkiye
• Project SATURN- a real-world evidence data collaboration with existing European datasets in Osteogenesis Imperfecta to support future therapies
• Pseudoarthrosis of the Distal Humerus in Pediatric Osteogenesis Imperfecta Patients: A Case Series and Literature Review
• Rare coexistence of hypopituitarism with osteogenesis imperfecta - A double-trouble for bone
• Resilience and coping: a qualitative analysis of cognitive and behavioral factors in adults with osteogenesis Imperfecta
• Response to Letter to the Editor from Bala and Dayal: "Safety and Efficacy of Denosumab in Children With Osteogenesis Imperfecta - the First Prospective Comparative Study"
• Reviewing hereditary connective tissue disorders: Proposals of harmonic medicolegal assessments
• Root resorption of primary molars and dental development of premolars in children with Osteogenesis Imperfecta medicated with bisphosphonates, grouped according to age and gender
• Sclerostin antibody enhances implant osseointegration in bone with Col1a1 mutation
• Sclerostin inhibition in rare bone diseases: Molecular understanding and therapeutic perspectives
• Setrusumab for the Treatment of Osteogenesis Imperfecta: 12-Month Results from the Phase 2b Asteroid Study
• Severity of acute phase reaction in children receiving the first dose of zoledronic acid and the impact of the underlying condition: a cross-sectional study
• Skeletal and Non-skeletal Phenotypes in Children with Osteogenesis Imperfecta
• Skeletal pathology in mouse models of Gould syndrome is partially alleviated by genetically reducing TGFβ signaling
• Surgical treatment of scoliosis in patients with osteogenesis imperfecta: a single institution case series
• The Creation of an Individualized School Plan for Optimal Inclusion of Students with Osteogenesis Imperfecta
• The IFITM5 mutation in osteogenesis imperfecta type V is associated with an ERK/SOX9-dependent osteoprogenitor differentiation defect
• The impact of foot orthoses on gait in children with Osteogenesis Imperfecta type I, III and IV - a cross-sectional study
• The IMPACT Survey: the economic impact of osteogenesis imperfecta in adults
• The PATCH study: Prevalence of Hearing Loss During Ageing and Treatment Choices in Osteogenesis Imperfecta: A Danish Nationwide Register-Based Cohort Study
• The vitamin D status in a Chinese osteogenesis imperfecta population and its correlation with bone metabolic markers and bone density
• Unraveling the genetic collagen connection: clinical and therapeutic insights on genetic connective tissue disorders
• Unraveling the Link of Altered TGFbeta Signaling with Scoliotic Vertebral Malformations in Osteogenesis Imperfecta: A Comprehensive Review
• Update on the Genetics of Osteogenesis Imperfecta