Eymard B - Search Results

1

Eymard B, Camdessanché JP. Eymard B, et al. Rev Neurol (Paris). 2016 Oct;172(10):537-538. doi: 10.1016/j.neurol.2016.09.006. Rev Neurol (Paris). 2016. PMID: 27725097 No abstract available.

2

[Clinical and electrophysiologic study of the peripheral nerve in 28 cases of mitochondrial disease].

Eymard B, Penicaud A, Leger JM, Romero N, Marsac C, Fardeau M, Brunet P. Eymard B, et al. Rev Neurol (Paris). 1991;147(6-7):508-12. Rev Neurol (Paris). 1991. PMID: 1660183 French.

3

[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy].

Marsac C, Degoul F, Bonne G, Romero N, Nelson I, Fardeau M, François D, Ponsot G, Harpey JP, Eymard B, et al. Marsac C, et al. Among authors: eymard b. Rev Neurol (Paris). 1991;147(6-7):462-6. Rev Neurol (Paris). 1991. PMID: 1962051 French.

4

[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene].

Fardeau M, Vicart P, Caron A, Chateau D, Chevallay M, Collin H, Chapon F, Duboc D, Eymard B, Tomé FM, Dupret JM, Paulin D, Guicheney P. Fardeau M, et al. Among authors: eymard b. Rev Neurol (Paris). 2000 May;156(5):497-504. Rev Neurol (Paris). 2000. PMID: 10844369 French.

5

[A patient with suspected muscle disease?].

Eymard B, Laforêt P. Eymard B, et al. Rev Neurol (Paris). 2003 Jan;159(1):114-21. Rev Neurol (Paris). 2003. PMID: 12618663 Review. French. No abstract available.

6

[Myopathy-lipomatosis associated with A8344G mitochondrial DNA mutation].

Auré K, Sternberg D, Maisonobe T, Herson S, Jardel C, Blondy P, Lombès A, Eymard B, Laforêt P. Auré K, et al. Among authors: eymard b. Rev Neurol (Paris). 2003 Dec;159(12):1163-8. Rev Neurol (Paris). 2003. PMID: 14978417 French.

7

[Congenital myasthenic syndromes: phenotypic expression and pathophysiological characterisation].

Andreux F, Hantaï D, Eymard B. Andreux F, et al. Among authors: eymard b. Rev Neurol (Paris). 2004 Feb;160(2):163-76. doi: 10.1016/s0035-3787(04)70887-5. Rev Neurol (Paris). 2004. PMID: 15034473 Review. French.

8

[Exercise-intolerance and exercise-induced rhabdomyolisis: etiology and diagnosis].

Laforêt P, Eymard B. Laforêt P, et al. Among authors: eymard b. Rev Neurol (Paris). 2004 Feb;160(2):217-23. doi: 10.1016/s0035-3787(04)70894-2. Rev Neurol (Paris). 2004. PMID: 15034480 Review. French.

9

[Autosomal dominant limb-girdle muscular dystrophy associated with conduction defects (LGMD1B): a description of 8 new families with the LMNA gene mutations].

Ben Yaou R, Bécane HM, Demay L, Laforet P, Hannequin D, Bohu PA, Drouin-Garraud V, Ferrer X, Mussini JM, Ollagnon E, Petiot P, Penisson-Besnier I, Streichenberger N, Toutain A, Richard P, Eymard B, Bonne G. Ben Yaou R, et al. Among authors: eymard b. Rev Neurol (Paris). 2005 Jan;161(1):42-54. doi: 10.1016/s0035-3787(05)84972-0. Rev Neurol (Paris). 2005. PMID: 15678000 French.

10

[Atypical ocular myasthenia gravis].

Milea D, Laforet P, Eymard B. Milea D, et al. Among authors: eymard b. Rev Neurol (Paris). 2005 May;161(5):543-8. doi: 10.1016/s0035-3787(05)85088-x. Rev Neurol (Paris). 2005. PMID: 16106805 French.

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