Urinary pyridinoline cross-links as biomarkers of osteogenesis imperfecta

Autor: Matthias R. Baumgartner, Uschi Lindert, Marius E. Kraenzlin, Cecilia Giunta, Ana Belinda Campos-Xavier, Marianne Rohrbach, Luisa Bonafé

Publikováno v: Orphanet Journal of Rare Diseases
Orphanet journal of rare diseases
Orphanet Journal of Rare Diseases, vol. 10, no. 1, pp. 104

Osteogenesis imperfecta (OI) is a group of genetic heterogeneous connective tissue disorders characterized by increased bone fragility and susceptibility to fractures. Laboratory diagnosis relies on time-consuming and cost-intensive biochemical and m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::983755078d093b98c7da2fe02dd3e4d0
http://europepmc.org/articles/PMC4549897