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Unusual association of amyotrophic lateral sclerosis and myasthenia gravis: A dysregulation of the adaptive immune system?
Del Mar Amador M, Vandenberghe N, Berhoune N, Camdessanché JP, Gronier S, Delmont E, Desnuelle C, Cintas P, Pittion S, Louis S, Demeret S, Lenglet T, Meininger V, Salachas F, Pradat PF, Bruneteau G. Del Mar Amador M, et al. Among authors: delmont e. Neuromuscul Disord. 2016 Jun;26(6):342-6. doi: 10.1016/j.nmd.2016.03.004. Epub 2016 Mar 29. Neuromuscul Disord. 2016. PMID: 27102004
[Castleman's disease located in the central nervous system].
Delmont E, Lonjon M, Michiels JF, Chanalet S, Bourg V, Xerri L, Bondiau PY, Lebrun C. Delmont E, et al. Rev Neurol (Paris). 2003 May;159(5 Pt 1):581-5. Rev Neurol (Paris). 2003. PMID: 12773906 Review. French.
[Mills' syndrome: a rare clinical entity].
Lachaud S, Soriani MH, Delmont E, Budai M, Desnuelle C, Lebrun C. Lachaud S, et al. Among authors: delmont e. Rev Neurol (Paris). 2007 Mar;163(3):335-40. doi: 10.1016/s0035-3787(07)90405-1. Rev Neurol (Paris). 2007. PMID: 17404520 French.
Substitutions at residue 211 in the prion protein drive a switch between CJD and GSS syndrome, a new mechanism governing inherited neurodegenerative disorders.
Peoc'h K, Levavasseur E, Delmont E, De Simone A, Laffont-Proust I, Privat N, Chebaro Y, Chapuis C, Bedoucha P, Brandel JP, Laquerriere A, Kemeny JL, Hauw JJ, Borg M, Rezaei H, Derreumaux P, Laplanche JL, Haïk S. Peoc'h K, et al. Among authors: delmont e. Hum Mol Genet. 2012 Dec 15;21(26):5417-28. doi: 10.1093/hmg/dds377. Epub 2012 Sep 10. Hum Mol Genet. 2012. PMID: 22965875
134 results