Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Imbert, Laurianne"'
Autor:
Imbert, Laurianne
L’Ostéogénèse Imparfaite (OI) est une maladie génétique dont une des conséquences est la fragilité accrue du squelette, lui valant ainsi le nom de « maladie des os de verre ». Il existe plusieurs phénotypes reflétant différents niveaux
Externí odkaz:
http://www.theses.fr/2014ECDL0042/document
Autor:
Koral, Jerome, Fanget, Marie, Imbert, Laurianne, Besson, Thibault, Kennouche, Djahid, Parent, Audrey, Foschia, Clément, Rossi, Jérémy, Millet, Guillaume Y.
Publikováno v:
International Journal of Sports Physiology & Performance; Jan2022, Vol. 17 Issue 1, p67-77, 11p, 1 Black and White Photograph, 1 Diagram, 3 Charts, 2 Graphs
Autor:
Masci, Marco, Wang, Min, Imbert, Laurianne, Barnes, Aileen M., Spevak, Lyudmila, Lukashova, Lyudmila, Huang, Yihe, Ma, Yan, Marini, Joan C., Jacobsen, Christina M., Warman, Matthew L., Boskey, Adele L.
Publikováno v:
In Bone June 2016 87:120-129
Publikováno v:
In Journal of the Mechanical Behavior of Biomedical Materials June 2015 46:261-270
Publikováno v:
In Bone August 2014 65:18-24
Autor:
Donnelly, Patrick E.1,2, Imbert, Laurianne3, Culley, Kirsty L.1, Warren, Russell F.1, Chen, Tony1,2, Maher, Suzanne A.1,2 MaherS@hss.edu
Publikováno v:
Journal of Biomaterials Science -- Polymer Edition. Feb2019, Vol. 30 Issue 3, p215-232. 18p. 1 Color Photograph, 1 Diagram, 1 Chart, 5 Graphs.
Autor:
Imbert, Laurianne1 laurianne.imbert@gmail.com, Gourion-Arsiquaud, Samuel2, Villarreal-Ramirez, Eduardo3, Spevak, Lyudmila1, Taleb, Hayat1, van der Meulen, Marjolein C. H.1,4,5, Mendelsohn, Richard6, Boskey, Adele L.1,7
Publikováno v:
PLoS ONE. 9/4/2018, Vol. 13 Issue 9, p1-15. 15p.
Autor:
Boskey, Adele L.1,2, Imbert, Laurianne1 imbertL@hss.edu
Publikováno v:
Annals of the New York Academy of Sciences. Dec2017, Vol. 1410 Issue 1, p93-106. 14p.
Autor:
Imbert, Laurianne
Publikováno v:
Autre. Ecole Centrale de Lyon, 2014. Français. ⟨NNT : 2014ECDL0042⟩
Osteogenesis Imperfecta (OI) is a genetic disorder, also known as the “brittle bone disease”, associated with an increased bone fragility. Several phenotypes exist, reflecting different severities but some features are frequently observed like a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3a9cf7b9cf9941ab9cff60cc4c7982ab
https://tel.archives-ouvertes.fr/tel-01146241/file/TH_T2420_limbert.pdf
https://tel.archives-ouvertes.fr/tel-01146241/file/TH_T2420_limbert.pdf
Autor:
Boyer, Bertrand, Geringer, Jean, Philippot, Rémi, Di Lorio, Alexandre, Néri, Thomas, Ahmad, Ola, Imbert, Laurianne, Farizon, Frédéric
Publikováno v:
Proceedings of the 14th EFORT Congress 2013 (European Federation of National Associations of Orthopaedic Sports Traumatology)
14th EFORT Congress 2013 (European Federation of National Associations of Orthopaedic Sports Traumatology)
14th EFORT Congress 2013 (European Federation of National Associations of Orthopaedic Sports Traumatology), Jun 2013, Istamboul, Turkey. pp.En attente
14th EFORT Congress 2013 (European Federation of National Associations of Orthopaedic Sports Traumatology)
14th EFORT Congress 2013 (European Federation of National Associations of Orthopaedic Sports Traumatology), Jun 2013, Istamboul, Turkey. pp.En attente
International audience; En attente
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b3207c15e6de2848a44bcecb3cc07bd8
https://hal.archives-ouvertes.fr/hal-00932663
https://hal.archives-ouvertes.fr/hal-00932663