Disease: Osteogenesis imperfecta- type 7
- Analysis of COL1A1 and COL1A2 gene variants in two fetuses with osteogenesis imperfecta
- Bone allografting: an original method for biological osteosynthesis and bone reinforcement in children with osteogenesis imperfecta
- Case Report: A Novel Homozygous Variant of the <em>SERPINF1</em> Gene in Rare Osteogenesis Imperfecta Type VI
- Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate
- Clinical and genetic characteristics of 9 rare cases with coexistence of dual genetic diagnoses
- CRTAP deficiency leads to abnormally high bone matrix mineralization in a murine model and in children with osteogenesis imperfecta type VII
- Cyclic intravenous pamidronate for an infant with osteogenesis imperfecta type II
- Deep intronic mutation in CRTAP results in unstable isoforms of the protein to induce type I collagen aggregation in a lethal type of osteogenesis imperfecta type VII
- Dental and craniofacial defects in the Crtap(-/-) mouse model of osteogenesis imperfecta type VII
- Dental and craniofacial defects in the Crtap<sup>-/-</sup> mouse model of osteogenesis imperfecta type VII
- Genotype-phenotype relationship and comparison between eastern and western patients with osteogenesis imperfecta
- Intracranial aneurysm as a possible complication of osteogenesis imperfecta: a case series and literature review
- Intravenous pamidronate in osteogenesis imperfecta type VII
- Keratoconus tomographic indices in osteogenesis imperfecta
- Mitigating the Denosumab-Induced Rebound Phenomenon with Alternating Short- and Long-Acting Anti-resorptive Therapy in a Young Boy with Severe OI Type VI
- Osteogenesis imperfecta type VII maps to the short arm of chromosome 3
- Osteogenesis imperfecta type VII: an autosomal recessive form of brittle bone disease
- Osteogenesis imperfecta type VIII: highlighting the need for genetic testing
- Outcomes of Pediatric Osteogenesis Imperfecta Patients Requiring Port-a-Cath Placement for Long-Term Vascular Access
- Prevalence of Monogenic Bone Disorders in a Dutch Cohort of Atypical Femur Fracture Patients
- RNA Sequencing of Urine-Derived Cells for the Characterization and Diagnosis of Osteogenesis Imperfecta
- TAPT1-at the crossroads of extracellular matrix and signaling in Osteogenesis imperfecta
- Whole-Body Metabolism and the Musculoskeletal Impacts of Targeting Activin A and Myostatin in Severe Osteogenesis Imperfecta