Latest papers

Mutations in COL1A1 of type I collagen genes in Chinese patients with osteogenesis imperfecta.

Bruck syndrome: osteogenesis imperfecta and arthrogryposis multiplex congenita.

Osteogenesis imperfecta: recent findings shed new light on this once well-understood condition.

Alendronate treatment of the brtl osteogenesis imperfecta mouse improves femoral geometry and load response before fracture but decreases predicted material properties and has detrimental effects on osteoblasts and bone formation.

Alternative Indications for Bisphosphonate Therapy

Osteogenesis imperfecta in a 3,000-year-old mummy.

Telescoping versus non-telescoping rods in the treatment of osteogenesis imperfecta.

Modified Sofield-Millar operation: less invasive surgery of lower limbs in osteogenesis imperfecta.

Large osteoclasts in pediatric osteogenesis imperfecta patients receiving intravenous pamidronate.

Intravenous pamidronate in osteogenesis imperfecta type VII.

Osteogenesis imperfecta type III with intracranial hemorrhage and brachydactyly associated with mutations in exon 49 of COL1A2.

The Association of Connective Tissue Disorders with Cervical Artery Dissections

[Bisphosphonates and other new therapeutic agents for the treatmednt of osteogenesis imperfecta].

Oral findings in adults with osteogenesis imperfecta.

[Osteogenesis imperfecta].

Augmentation of the mandible via a tent-pole procedure and implant treatment in a patient with type III osteogenesis imperfecta: clinical and histologic considerations.

Osteogenesis imperfecta.

A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with osteogenesis imperfecta.

CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta.

Results and complications of a surgical technique for correction of coxa vara in children with osteopenic bones.