Disease: Osteogenesis imperfecta
- A bimolecular modification strategy for developing long-lasting bone anabolic aptamer
- A Case of Acute Cholecystitis Successfully Treated With Endoscopic Ultrasound-Guided Gallbladder Drainage in a Patient With Osteogenesis Imperfecta
- A homozygous SP7/OSX mutation causes osteogenesis and dentinogenesis imperfecta with craniofacial anomalies
- A novel compound heterozygous variation in the <em>FKBP10</em> gene causes Bruck syndrome without congenital contractures: A case report
- A novel sliding double flexible intramedullary nail technique for the management of lower extremity long bone fractures and deformities in osteogenesis imperfecta
- A practical guide to the diagnosis and management of osteoporosis in childhood and adolescence
- A pregnant patient with type II osteogenesis imperfecta pregnancy
- A Sporadic Case of <em>COL1A1</em> Osteogenesis Imperfecta: From Prenatal Diagnosis to Outcomes in Infancy-Case Report and Literature Review
- AAV-based gene editing of type 1 collagen mutation to treat osteogenesis imperfecta
- Access to care among patients with osteogenesis imperfecta during the COVID-19 pandemic
- Acetabular Fracture in a Skeletally Mature Patient With Osteogenesis Imperfecta Treated With Open Reduction Internal Fixation: A Case Report
- Advantages of Using 3D Spheroid Culture Systems in Toxicological and Pharmacological Assessment for Osteogenesis Research
- An Analysis From a Tertiary Pediatric Hospital: Does Physical Activity Play a Role in the Management of Children and Young Adults With Osteogenesis Imperfecta?
- An FGFR2 mutation as the potential cause of a new phenotype including early-onset osteoporosis and bone fractures: a case report
- Assessing type I collagen expression and quality in cellular models of osteogenesis imperfecta
- Association of antenatal evaluations with postmortem and genetic findings in the series of fetal osteogenesis imperfecta
- Asymptomatic Infant Rib Fractures Are Primarily Non-abuse-Related and Should Not Be Used to Assess Physical Child Abuse
- Atypical cell death and insufficient matrix organization in long-bone growth plates from Tric-b-knockout mice
- Bleeding assessment in a large cohort of patients with Osteogenesis Imperfecta
- Bone microarchitecture and strength assessment in adults with osteogenesis imperfecta using HR-pQCT: normative comparison and challenges
- Bronchial obstruction in osteogenesis imperfecta can be detected by forced oscillation technique
- Case Report: A novel <em>de novo</em> variant of <em>COL1A1</em> in fetal genetic osteogenesis imperfecta
- Case Report: A novel de novo variant of COL1A1 in fetal genetic osteogenesis imperfecta
- Caution with noninvasive prenatal screening for single gene disorders: A case report of a COL1A1 variant in osteogenesis imperfecta
- Characteristics of femoral neck fractures in osteogenesis imperfecta: Series of four-teen consecutive hips in twelve patients
- Col1A-2 Mutation in Osteogenesis Imperfecta Mice Contributes to Long Bone Fragility by Modifying Cell-Matrix Organization
- Combining anabolic loading and raloxifene improves bone quantity and some quality measures in a mouse model of osteogenesis imperfecta
- Correction: The impact of osteogenesis imperfecta severity on oral health-related quality of life in Spain: a cross-sectional study
- Corrosion of a Fassier-Duval Telescopic Nail Causing Pain and Osteolysis: A Case Report
- Current and Developing Pharmacologic Agents for Improving Skeletal Health in Adults with Osteogenesis Imperfecta
- Demographics and medical burden of osteogenesis imperfecta: a nationwide database analysis
- Development of AAV-Mediated Gene Therapy Approaches to Treat Skeletal Diseases
- Discrepancies in the Phenotypical Classification of Osteogenesis Imperfecta in a Patient with COL1A2 Mutation: A Case Report
- Echocardiographic abnormalities and joint hypermobility in Chinese patients with Osteogenesis imperfecta
- Editorial: Fish as model organism for skeletal diseases
- Efficacy and safety of denosumab versus zoledronic acid in OI adults: A prospective, open-label, randomized study
- Emerging Landscape of Osteogenesis Imperfecta Pathogenesis and Therapeutic Approaches
- Epidemiological Assessment of a Pediatric Palliative Care Clinic at a Brazilian Quaternary Hospital: 20 Years of Experience
- Evaluation of functionality-mobility in patients with skeletal dysplasias. Application of the STEMS tool ("everyday symptoms and mobility screening tool for skeletal dysplasias")
- Exome sequencing identified mutations in the WNT1 and COL1A2 genes in osteogenesis imperfecta cases
- Exploring the Implications of Golgi Apparatus Dysfunction in Bone Diseases
- Extra-Skeletal Manifestations in Osteogenesis Imperfecta Mouse Models
- Extracellular matrix protein composition dynamically changes during murine forelimb development
- Fatality owing to pulmonary hemorrhage following pamidronate disodium administration in a neonate with osteogenesis imperfecta type 2: A case report
- Features and results of surgical rehabilitation of hearing loss in osteogenesis imperfecta
- Generation of skin-derived iPSCs from an Osteogenesis imperfecta patient carrying WNT1(c.677C>T) mutation
- Generation of skin-derived iPSCs from an Osteogenesis imperfecta patient carrying WNT1<sup>c.677C>T</sup> mutation
- Genetic analysis, phenotype spectrum and functional study of rare osteogenesis imperfecta caused by CRTAP Variants
- Genetic basis of osteogenesis imperfecta from a single tertiary centre in South Africa
- Genotypic Characterization of a Chinese Family with Osteogenesis Imperfecta and Generation of Disease-Specific Induced Pluripotent Stem Cells
- Health-related quality of life and fatigue in adult rare bone disease patients: A cross-sectional study from Austria
- Home care needs assessment among caregivers of children and adolescents with osteogenesis imperfecta: a cross-sectional study
- Identification of a family with van der Hoeve's syndrome harboring a novel COL1A1 mutation and generation of patient-derived iPSC lines and CRISPR/Cas9-corrected isogenic iPSCs
- Imaging in osteogenesis imperfecta: Where we are and where we are going
- Impaired muscle parameters in adults with mild to severe types of osteogenesis imperfecta: a cross-sectional study
- In Vitro Modelling of Osteogenesis Imperfecta with Patient-Derived Induced Mesenchymal Stem Cells
- In Vivo Assessment of Skin Surface Pattern: Exploring Its Potential as an Indicator of Bone Biomechanical Properties
- Influence of zoledronic acid and pamidronate on tooth eruption in children with osteogenesis imperfecta
- Informed Inclusion Model: Medical Student Wheelchair User in an Obstetrics and Gynecology Clerkship
- Is Osteogenesis Imperfecta Associated with Cardiovascular Abnormalities? A Systematic Review of the Literature
- Isolated dentinogenesis imperfecta: Novel DSPP variants and insights on genetic counselling
- KDELR2 promotes bone marrow mesenchymal stem cell osteogenic differentiation via GSK3β/β-catenin signaling pathway
- Medical Management for Fracture Prevention in Children with Osteogenesis Imperfecta
- Medication-related osteonecrosis of the jaw in a paediatric patient taking denosumab: a case report
- Metabolic bone diseases : what's new in 2023
- New Perspectives of Therapies in Osteogenesis Imperfecta-A Literature Review
- Ocular manifestations suggest osteogenesis imperfecta in a previously undiagnosed adult following polytrauma
- Osteogenesis Imperfecta and Split Foot Malformation due to 7q21.2q21.3 Deletion Including COL1A2, DLX5/6 Genes: Review of the Literature
- Osteogenesis imperfecta: a cross-sectional study of skeletal and extraskeletal features in a large cohort of Italian patients
- Osteogenesis imperfecta: an unusual presentation
- Osteoid osteoma appearing after bony fracture in a girl with osteogenesis imperfecta
- Osteoporosis Improved by Romosozumab Therapy in a Patient With Type I Osteogenesis Imperfecta
- Otic Capsule Demineralization and Hearing Outcome of Stapes Surgery for Osteogenesis Imperfecta in Comparison With Otosclerosis
- Physiological cell bioprinting density in human bone-derived cell-laden scaffolds enhances matrix mineralization rate and stiffness under dynamic loading
- Postoperative screw pullout of severe spondylolisthesis in osteogenesis imperfecta: a case report with 3-year follow-up
- Preclinical rodent models for human bone disease including a focus on cortical bone
- Prenatal ultrasound findings and prenatal diagnosis of fetal skeletal dysplasia
- Psychosocial Outcomes of Pain and Pain Management in Adults with Osteogenesis Imperfecta: A Qualitative Study
- Quadratus Lumborum Block for Ovarian Cystectomy Surgery in a Patient With Severe Kyphoscoliosis
- Risk perception for fractures and its related factors among family caregivers of underage patients with osteogenesis imperfecta in China: A cross-sectional study
- RNA-based bone histomorphometry: method and its application to explaining postpubertal bone gain in a G610C mouse model of osteogenesis imperfecta
- Safety and Efficacy of Denosumab in Children With Osteogenesis Imperfecta-the First Prospective Comparative Study
- Short-term effects of Mediterranean diet on nutritional status in adults affected by Osteogenesis Imperfecta: a pilot study
- Spontaneous Corneal Clearing after Descemet Membrane Rupture and Near-Total Detachment in Keratoglobus: A Case Report
- Surgical treatment of osteogenesis imperfecta: a summary of the incidence of femoral implant-related complications in children with Sillence type I, III and IV
- Tensile Mechanical Properties of Dry Cortical Bone Extracellular Matrix: A Comparison Among Two Osteogenesis Imperfecta and One Healthy Control Iliac Crest Biopsies
- The diagnostic odyssey of a patient with dihydropyrimidinase deficiency: a case report and review of the literature
- The impact of craniofacial and dental osteogenesis imperfecta manifestations on oral health-related quality of life of children and adolescents
- The impact of osteogenesis imperfecta severity on oral health-related quality of life in Spain: a cross-sectional study
- The IMPACT survey: a mixed methods study to understand the experience of children, adolescents and adults with osteogenesis imperfecta and their caregivers
- The Regulatory Network of CREB3L1 and Its Roles in Physiological and Pathological Conditions
- Transmembrane proteins with unknown function (TMEMs) as ion channels: electrophysiological properties, structure, and pathophysiological roles
- Trends in Serum Cytokine Expression in Pediatric Skeletal Dysplasia
- Type 1 collagen: Synthesis, structure and key functions in bone mineralization
- Unique quinoline orientations shape the modified aptamer to sclerostin for enhanced binding affinity and bone anabolic potential
- Unraveling the genetic collagen connection: clinical and therapeutic insights on genetic connective tissue disorders
- Use of Complementary and Alternative Medicine in Patients with Rare Bone Diseases and Osteoporosis
- Ventriculosubgaleal shunt placement for hydrocephalus in osteogenesis imperfecta with novel compound heterozygous CRTAP variants
- Z-osteotomy for uniplanar femoral shaft deformity correction in an adolescent with osteogenesis imperfecta
- Τhe story of sclerostin inhibition: the past, the present, and the future