Disease: Van Buchem disease type 2 (VBCH2)
- Adult Osteopetrosis Type 2
- Altered collagen I and premature pulmonary embryonic differentiation in patients with OI type II
- Analysis of <em>N</em>-glycosylation protein of Kashin-Beck disease chondrocytes derived from induced pluripotent stem cells based on label-free strategies with LC-MS/MS
- 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
- CaMKII inhibition due to TRIC-B loss-of-function dysregulates SMAD signaling in osteogenesis imperfecta
- Intracranial aneurysm as a possible complication of osteogenesis imperfecta: a case series and literature review
- Modified ulnar lengthening for correction of the Masada type 2 forearm deformity in hereditary multiple exostosis
- Osteopetrosis with Arnold Chiari malformation type I
- Quality of life of pediatric and adult individuals with osteogenesis imperfecta: a meta-analysis
- RNA Sequencing of Urine-Derived Cells for the Characterization and Diagnosis of Osteogenesis Imperfecta
- Sclerostin: current knowledge and future perspectives
- Skeletal dysplasias of the fetus and infant: comprehensive review and our experience over a 10-year period
- Spondyloepimetaphyseal dysplasia with joint laxity type 2: Aggregating the literature and reporting on the life of a 66-year-old man
- Targeted deletion of Sost distal enhancer increases bone formation and bone mass
- Tibial plateau fracture and RNA sequencing with osteogenesis imperfecta: a case report
- Trichorhinophalangeal syndrome type 1 (TRPS1) expression in male breast carcinoma
- Worth syndrome as a diagnosis for mandibular osteosclerosis