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Showing 1-7 of 7 results

  1. A Dyadic Nosology for Osteogenesis Imperfecta and Bone Fragility Syndromes 2024

    In 2023 following extensive consultation with key stakeholders, the expert Nosology Working Group of the International Skeletal Dysplasia Society...

    David Owen Sillence in Calcified Tissue International
    Article Open access 28 June 2024

  2. Novel Mutations in PLOD2 Cause Rare Bruck Syndrome

    Bruck syndrome is a rare autosomal recessive form of osteogenesis imperfecta (OI), which is mainly characterized by joint contractures and recurrent...

    Fang Lv, **aojie Xu, ... Mei Li in Calcified Tissue International
    Article 24 November 2017

  4. The Role of Collagen Organization on the Properties of Bone

    Bone is a complex tissue constituted by a collagen matrix filled in with crystal of hydroxyapatite (HAP). Bone mechanical properties are influenced...

    Patrick Garnero in Calcified Tissue International
    Article 17 April 2015

  5. Recent Advances in Osteogenesis Imperfecta

    “Osteogenesis imperfecta” is a term used to describe a group of genetic disorders of variable phenotype usually defined by recurrent fractures, low...

    Tim Cundy in Calcified Tissue International
    Article 27 March 2012

  7. Alteration in the Extent of Collagen I Hydroxylation, Isolated from Femoral Heads of Women with a Femoral Neck Fracture Caused by Osteoporosis

    The aim of this study was to investigate the extent of lysyl and prolyl hydroxylation of collagen I in osteoporosis and compare it with collagen I...

    J. Köwitz, M. Knippel, ... J. Mach in Calcified Tissue International
    Article 01 June 1997
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