Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Alice Fassier"'
Autor:
Kariman Abelin-genevois, Philippe Beaudet, Benjamin Blondel, Véronique Bourg, Emeline Bourgeois, Bertrand Boyer, Jean Brilhault, Adeline Cambon-binder, Céline Cazorla, Jean-michel Cognet, Olivier Cornu, Vincent Crenn, Klaus Dieterich, Alice Fassier, Stéphane Fuentes, Jeannot Gaudias, Louis-Etienne Gayet, Loïc Geffroy, Jacques Griffet, Denis Huten, Dragan Jeremic, Jean-Christophe Lambotte, François Lintz, Julie Manon, Olivier Mares, Julien Maximen, Pierre Métais, Didier Moukoko, Xavier Ohl, Didier Ollat, Régis Pailhé, Sébastien Pesenti, Solène Prost, Dan Putineanu, Gérard Richardi, Charles Rivière, Mickaël Ropars, Renaud Siboni, Karim Tribak, Alexandre Tronchot, Patrick Tropiano, Tanguy Vendeuvre, Pascal-André Vendittoli, Loic Villet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00dfedaf5e9a69eb263db441b7c635e8
https://doi.org/10.1016/b978-2-294-77250-4.09994-0
https://doi.org/10.1016/b978-2-294-77250-4.09994-0
Autor:
Alice Fassier
Publikováno v:
Orthopaedics & Traumatology: Surgery & Research. 107:102759
Medical and surgical treatment of osteogenesis imperfecta has undergone two revolutions that improved quality of life and functional capacity: reduced bone absorption with the use of bisphosphonates, and improvement in internal fixation with the deve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::295fd2864f1f0f2f2d692d63966f5944
https://doi.org/10.1016/j.otsr.2020.102759
https://doi.org/10.1016/j.otsr.2020.102759
Autor:
Edith Bonnelye, Bruno Ranchin, Irma Machuca-Gayet, Justine Bacchetta, Martin Zenker, Delphine Farlay, Camille Beaufils, Caroline Freychet, Alice Fassier, Aurélia Bertholet-Thomas
Publikováno v:
BONE
BONE, 2018, 106, pp.187-193. ⟨10.1016/j.bone.2017.10.015⟩
BONE, Elsevier, 2018, 106, pp.187-193. ⟨10.1016/j.bone.2017.10.015⟩
BONE, 2018, 106, pp.187-193. ⟨10.1016/j.bone.2017.10.015⟩
BONE, Elsevier, 2018, 106, pp.187-193. ⟨10.1016/j.bone.2017.10.015⟩
Introduction Pierson syndrome is caused by a mutation of LAMB2, encoding for laminin β2. Clinical phenotype is variable but usually associates congenital nephrotic syndrome (CNS) and ocular abnormalities. Neuromuscular impairment has also been descr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc6a35dd2513fd11ad26a2193ec91c66
https://hal.science/hal-02354560
https://hal.science/hal-02354560
Purpose The aim of this retrospective long-term study was to review and present the effects of treatment for 11 children with arthrogryposis multiplex congenital, or amyoplasia, followed from birth until skeletal maturity. Methods We evaluated walkin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::522ecb823933a7d56b50cd9ed345068a
https://europepmc.org/articles/PMC2758174/
https://europepmc.org/articles/PMC2758174/
Ostéome ostéoïde de l’arrière fond du cotyle traité par forage résection osseux percutané : cinq cas
Autor:
Rémi Kohler, Sébastien Raux, Kariman Abelin-Genevois, Alice Fassier, Vincent Cunin, Isabelle Canterino, Franck Chotel
Publikováno v:
Revue de Chirurgie Orthopédique et Traumatologique. 98:S378
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a64aec207d07fd5ce1d968055f2170ce
https://doi.org/10.1016/j.rcot.2012.08.260
https://doi.org/10.1016/j.rcot.2012.08.260