Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Joëlle Tanniger"'
Autor:
Alexandra Lenoir, Bérengère Aubry-Rozier, Aline Bregou, Elena Gonzalez Rodriguez, Célia Paquier, Joëlle Tanniger, Mohamed Faouzi, Romain Lazor
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-12 (2024)
Abstract Background Osteogenesis imperfecta (OI) is a rare hereditary bone disease resulting from a defect in collagen synthesis or processing, leading to bone fragility, frequent fractures and skeletal deformities. OI is associated with increased re
Externí odkaz:
https://doaj.org/article/263fa2d3bb654868a4d760d3845bc245
Autor:
Lenoir, Alexandra1 (AUTHOR) alexandra.lenoir@med.uni-muenchen.de, Aubry-Rozier, Bérengère2 (AUTHOR) berengere.rozieraubry@hirslanden.ch, Bregou, Aline3 (AUTHOR) aline.bregou@chuv.ch, Gonzalez Rodriguez, Elena4 (AUTHOR) elena.gonzalez-rodriguez@chuv.ch, Paquier, Célia5 (AUTHOR) c.paquier@physioss.ch, Tanniger, Joëlle5 (AUTHOR) joelle.tanniger@chuv.ch, Faouzi, Mohamed6 (AUTHOR) mohamed.faouzi@unisante.ch, Lazor, Romain7,8 (AUTHOR) romain.lazor@chuv.ch
Publikováno v:
Orphanet Journal of Rare Diseases. 12/4/2024, Vol. 19 Issue 1, p1-12. 12p.