Disease: Osteogenesis imperfecta- type 1A
- A Multicenter Observational Cohort Study to Evaluate the Effects of Bisphosphonate Exposure on Bone Mineral Density and Other Health Outcomes in Osteogenesis Imperfecta
- A novel frameshift deletion in the COL1A1 gene identified in a Chinese family with osteogenesis imperfecta
- Characterization of a complex phenotype (fever-dependent recurrent acute liver failure and osteogenesis imperfecta) due to NBAS and P4HB variants
- Delivering a Home-Based Exercise Program to Youth With Osteogenesis Imperfecta: Protocol for a Comparative-Approach Study
- Dentinogenesis Imperfecta and Caries in Osteogenesis Imperfecta among Vietnamese Children
- Growth hormone therapy may increase fracture risk in a pubertal patient with osteogenesis imperfecta
- Management of hangman's fractures and a subaxial compression fracture in two children with osteogenesis imperfecta
- Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta
- Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VI
- Osteogenesis imperfecta Type 1: a case presentation with a new mutation in gene COL1A1
- Prenatal diagnosis of skeletal dysplasias: contribution of three-dimensional computed tomography
- Sickle cell disease with osteogenesis imperfecta
- Skeletal dysplasias of the fetus and infant: comprehensive review and our experience over a 10-year period
- Successful anterior cruciate ligament reconstruction and meniscal repair in osteogenesis imperfecta
- Total hip arthroplasty for Protrusio Acetabuli in a young adult Osteogenesis Imperfecta features and Marfanoid features: A case report
- Variable bone fragility associated with an Amish COL1A2 variant and a knock-in mouse model