Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Thomas Roels"'
Autor:
Mickaël Cardinal, Antoine Chretien, Thomas Roels, Sébastien Lafont, Michael S. Ominsky, Jean-Pierre Devogelaer, Daniel H. Manicourt, Catherine Behets
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Osteogenesis imperfecta (OI), which is most often due to a collagen type 1 gene mutation, is characterized by low bone density and bone fragility. In OI patients, gender-related differences were reported, but data in the literature are not convergent
Externí odkaz:
https://doaj.org/article/17cd81ff7d3843b595ac6ab978454a8f
Publikováno v:
Morphologie. 105:S1
Introduction Outre une grande fragilite osseuse, les patients atteints de la forme severe (type III) d’osteogenese imparfaite presentent un facies triangulaire, une protuberance fronto-parietale, un prognathisme relatif et de frequents os wormiens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbfeffb3e7c1498070c606af2903b230
https://doi.org/10.1016/j.morpho.2021.05.005
https://doi.org/10.1016/j.morpho.2021.05.005
Autor:
Michael S. Ominsky, Sébastien Lafont, Mickaël Cardinal, Alicia Dessain, Daniel Chappard, Thomas Roels, Guillaume Mabilleau, Daniel Manicourt, Jean-Pierre Devogelaer, Catherine Nyssen-Behets, Patrick Ammann
Publikováno v:
Calcified Tissue International
Calcified Tissue International, Springer Verlag, 2020, 106 (5), pp.494-508. ⟨10.1007/s00223-019-00655-5⟩
Calcified Tissue International, Springer Verlag, 2020, 106 (5), pp.494-508. ⟨10.1007/s00223-019-00655-5⟩
In osteogenesis imperfecta (OI), vertebrae brittleness causes thorax deformations and leads to cardiopulmonary failure. As sclerostin-neutralizing antibodies increase bone mass and strength in animal models of osteoporosis, their administration in tw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2ef7bd06cf621715621fe2dc6e4fed0
https://pubmed.ncbi.nlm.nih.gov/32025752
https://pubmed.ncbi.nlm.nih.gov/32025752
Autor:
Daniel Manicourt, Sébastien Lafont, Mickaël Cardinal, Janne Tys, Daniel Chappard, Thomas Roels, Jean-Pierre Devogelaer, Michael S. Ominsky, Guillaume Mabilleau, Catherine Nyssen-Behets, Patrick Ammann
Publikováno v:
Bone
Bone, 2019, 124, pp.137-147. ⟨10.1016/j.bone.2019.04.011⟩
Bone, Vol. 124 (2019) pp. 137-147
Bone, 2019, 124, pp.137-147. ⟨10.1016/j.bone.2019.04.011⟩
Bone, Vol. 124 (2019) pp. 137-147
International audience; Osteogenesis imperfecta type III (OI) is a serious genetic condition with poor bone quality and a high fracture rate in children. In a previous study, it was shown that a monoclonal antibody neutralizing sclerostin (Scl-Ab) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c2b29ba9ec5149b1cfbf2e6c9e898da
https://hal.univ-angers.fr/hal-02869317
https://hal.univ-angers.fr/hal-02869317
Autor:
Catherine Behets, Debluts Donovan, Louis Maistriaux, Jérôme Duisit, Pierre Gianello, Thomas Roels, Benoît Lengelé
Publikováno v:
Bulletin de l'Académie nationale de médecine, Vol. 202, no. 8-9, p. 1871-1882 (2018)
La mutilation digitale, unitaire ou multiple, a un impact critique sur la fonctionnalité de la main avec une diminution importante de la qualité de vie des patients. La reconstruction échappe souvent aux techniques avancées d’autotransplantatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f72f8589349a91069d91cb2162aa94f
https://hdl.handle.net/2078.1/218451
https://hdl.handle.net/2078.1/218451
Autor:
Cardinal, Mickaël, Chretien, Antoine, Roels, Thomas, Lafont, Sébastien, Ominsky, Michael S., Devogelaer, Jean-Pierre, Manicourt, Daniel H., Behets, Catherine
Publikováno v:
Frontiers in Genetics; 8/10/2021, Vol. 12, p1-12, 12p
Autor:
Cardinal, Mickaël, Dessain, Alicia, Roels, Thomas, Lafont, Sébastien, Ominsky, Michael S., Devogelaer, Jean-Pierre, Chappard, Daniel, Mabilleau, Guillaume, Ammann, Patrick, Nyssen-Behets, Catherine, Manicourt, Daniel H.
Publikováno v:
Calcified Tissue International; May2020, Vol. 106 Issue 5, p494-508, 15p
Publikováno v:
Transplant International; Sep2017 Supplement S2, Vol. 30, p577-612, 36p