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[Primary Moyamoya disease].
Echaniz-Laguna A, Degos B, Fleury MC, Beaujeux R, Tranchant C. Echaniz-Laguna A, et al. Among authors: fleury mc. Rev Neurol (Paris). 2002 Nov;158(11):1129-31. Rev Neurol (Paris). 2002. PMID: 12451349 French. No abstract available.
Phenotypic variability of aprataxin gene mutations.
Tranchant C, Fleury M, Moreira MC, Koenig M, Warter JM. Tranchant C, et al. Among authors: fleury m. Neurology. 2003 Mar 11;60(5):868-70. doi: 10.1212/01.wnl.0000048562.88536.a4. Neurology. 2003. PMID: 12629250
[Vogt-Koyanagi-Harada syndrome].
Blanc F, Fleury M, Talmant V, Deroide N, Szwarcberg J, Tranchant C. Blanc F, et al. Among authors: fleury m. Rev Neurol (Paris). 2005 Nov;161(11):1079-90. doi: 10.1016/s0035-3787(05)85175-6. Rev Neurol (Paris). 2005. PMID: 16288173 French.
[Ataxia associated with gluten sensitivity, myth or reality?].
Anheim M, Degos B, Echaniz-Laguna A, Fleury M, Grucker M, Tranchant C. Anheim M, et al. Among authors: fleury m. Rev Neurol (Paris). 2006 Feb;162(2):214-21. doi: 10.1016/s0035-3787(06)75002-0. Rev Neurol (Paris). 2006. PMID: 16518262 French.
A rare mimic of hereditary hemorrhagic telangiectasia and conjunctivitis.
Blanc F, Fleury M, Echaniz-Laguna A, Giraud S, Szwarcberg J, Tranchant C. Blanc F, et al. Among authors: fleury m. Ann Intern Med. 2007 Jan 16;146(2):150-1. doi: 10.7326/0003-4819-146-2-200701160-00018. Ann Intern Med. 2007. PMID: 17227945 No abstract available.
661 results