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Clinical phenotype of adult offspring carriers of the p.Pro392Leu mutation within the SQSTM1 gene in Paget's disease of bone.
Bone Rep. 2020 Sep 18;13:100717. doi: 10.1016/j.bonr.2020.100717. eCollection 2020 Dec.
Bone Rep. 2020.
PMID: 33015249
Free PMC article.
Gene-environment interactions in Paget's disease of bone.
Numan MS, Jean S, Dessay M, Gagnon E, Amiable N, Brown JP, Michou L.
Numan MS, et al. Among authors: dessay m.
Joint Bone Spine. 2019 May;86(3):373-380. doi: 10.1016/j.jbspin.2018.12.007. Epub 2018 Dec 27.
Joint Bone Spine. 2019.
PMID: 30594595
Free article.
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Attenuated clinical and osteoclastic phenotypes of Paget's disease of bone linked to the p.Pro392Leu/SQSTM1 mutation by a rare variant in the DOCK6 gene.
Dessay M, Couture E, Maaroufi H, Fournier F, Gagnon E, Droit A, Brown JP, Michou L.
Dessay M, et al.
BMC Med Genomics. 2022 Mar 3;15(1):41. doi: 10.1186/s12920-022-01198-9.
BMC Med Genomics. 2022.
PMID: 35241069
Free PMC article.
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[Cutaneous leishmaniasis of the vermilion border of the upper lip extending to the oral mucosa].
Elfatoiki FZ, Boumezzourh A, Maksouri H, Elkhalfaoui N, Dessay M, Riyad M, Chiheb S.
Elfatoiki FZ, et al. Among authors: dessay m.
Ann Dermatol Venereol. 2020 Feb;147(2):116-118. doi: 10.1016/j.annder.2019.09.600. Epub 2019 Oct 28.
Ann Dermatol Venereol. 2020.
PMID: 31672326
French.
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