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Page 1
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients.
Anheim M, Monga B, Fleury M, Charles P, Barbot C, Salih M, Delaunoy JP, Fritsch M, Arning L, Synofzik M, Schöls L, Sequeiros J, Goizet C, Marelli C, Le Ber I, Koht J, Gazulla J, De Bleecker J, Mukhtar M, Drouot N, Ali-Pacha L, Benhassine T, Chbicheb M, M'Zahem A, Hamri A, Chabrol B, Pouget J, Murphy R, Watanabe M, Coutinho P, Tazir M, Durr A, Brice A, Tranchant C, Koenig M. Anheim M, et al. Among authors: fleury m, m zahem a. Brain. 2009 Oct;132(Pt 10):2688-98. doi: 10.1093/brain/awp211. Epub 2009 Aug 20. Brain. 2009. PMID: 19696032
[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.
664 results