Fleury MC - Search Results

1

Spastic paraplegia due to recessive or dominant mutations in ERLIN2 can convert to ALS.

Amador MD, Muratet F, Teyssou E, Banneau G, Danel-Brunaud V, Allart E, Antoine JC, Camdessanché JP, Anheim M, Rudolf G, Tranchant C, Fleury MC, Bernard E, Stevanin G, Millecamps S. Amador MD, et al. Among authors: fleury mc. Neurol Genet. 2019 Nov 13;5(6):e374. doi: 10.1212/NXG.0000000000000374. eCollection 2019 Dec. Neurol Genet. 2019. PMID: 32042907 Free PMC article.

2

[Digestive tract disorders revealing mitochondrial cytopathy: MNGIE syndrome].

Chaury F, Fleury M, Tranchant C. Chaury F, et al. Rev Neurol (Paris). 2002 Jan;158(1):111-3. Rev Neurol (Paris). 2002. PMID: 11938332 French. No abstract available.

3

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

4

[Acute relapse in Charcot-Marie-Tooth 1B neuropathy: can protein P0 behave like an autoantigen?].

Fleury M, Anheim M, Tranchant C, Warter JM. Fleury M, et al. Rev Neurol (Paris). 2004 Sep;160(8-9):839-42. doi: 10.1016/s0035-3787(04)71042-5. Rev Neurol (Paris). 2004. PMID: 15454874 French.

5

[A clinical, neurophysiological and molecular study of 12 patients from 4 families with spinal and bulbar muscular atrophy].

Echaniz-Laguna A, Rousso E, Anheim M, Fleury M, Cossée M, Tranchant C. Echaniz-Laguna A, et al. Rev Neurol (Paris). 2005 Apr;161(4):437-44. doi: 10.1016/s0035-3787(05)85073-8. Rev Neurol (Paris). 2005. PMID: 15924079 French.

6

[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. Rev Neurol (Paris). 2006 Feb;162(2):214-21. doi: 10.1016/s0035-3787(06)75002-0. Rev Neurol (Paris). 2006. PMID: 16518262 French.

7

[Non-traumatic medullary compression and cauda equina].

Fleury MC, Tranchant C. Fleury MC, et al. Rev Prat. 2006 Feb 28;56(4):419-23. Rev Prat. 2006. PMID: 16629091 Review. French. No abstract available.

8

[Autosomal recessive spastic ataxia of Charlevoix-Saguenay: study of a family and review of the literature].

Anheim M, Chaigne D, Fleury M, Santorelli FM, De Sèze J, Durr A, Brice A, Koenig M, Tranchant C. Anheim M, et al. Rev Neurol (Paris). 2008 Apr;164(4):363-8. doi: 10.1016/j.neurol.2008.02.001. Epub 2008 Mar 25. Rev Neurol (Paris). 2008. PMID: 18439928 French.

9

[Severe generalized dystonia due to postradiotherapy cerebral calcifications].

Chanson JB, Anheim M, Lagha-Boukbiza O, Fleury M, Sellal F, Tranchant C. Chanson JB, et al. Rev Neurol (Paris). 2008 May;164(5):477-80. doi: 10.1016/j.neurol.2008.02.030. Epub 2008 Apr 1. Rev Neurol (Paris). 2008. PMID: 18555882 French.

10

Clinical and molecular findings of ataxia with oculomotor apraxia type 2 in 4 families.

Anheim M, Fleury MC, Franques J, Moreira MC, Delaunoy JP, Stoppa-Lyonnet D, Koenig M, Tranchant C. Anheim M, et al. Among authors: fleury mc. Arch Neurol. 2008 Jul;65(7):958-62. doi: 10.1001/archneur.65.7.958. Arch Neurol. 2008. PMID: 18625865

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