Eymard B - Search Results

1

Clinical heterogeneity and phenotype/genotype findings in 5 families with GYG1 deficiency.

Ben Yaou R, Hubert A, Nelson I, Dahlqvist JR, Gaist D, Streichenberger N, Beuvin M, Krahn M, Petiot P, Parisot F, Michel F, Malfatti E, Romero N, Carlier RY, Eymard B, Labrune P, Duno M, Krag T, Cerino M, Bartoli M, Bonne G, Vissing J, Laforet P, Petit FM. Ben Yaou R, et al. Among authors: eymard b. Neurol Genet. 2017 Dec 18;3(6):e208. doi: 10.1212/NXG.0000000000000208. eCollection 2017 Dec. Neurol Genet. 2017. PMID: 29264399 Free PMC article.

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

Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.

Degoul F, Nelson I, Lestienne P, Francois D, Romero N, Duboc D, Eymard B, Fardeau M, Ponsot G, Paturneau-Jouas M, et al. Degoul F, et al. Among authors: eymard b. J Neurol Sci. 1991 Feb;101(2):168-77. doi: 10.1016/0022-510x(91)90042-6. J Neurol Sci. 1991. PMID: 1851820

4

[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.

5

Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscle.

Romero NB, Lestienne P, Marsac C, Paturneau-Jouas M, Nelson I, François D, Eymard B, Fardeau M. Romero NB, et al. Among authors: eymard b. J Neurol Sci. 1989 Nov;93(2-3):297-309. doi: 10.1016/0022-510x(89)90199-8. J Neurol Sci. 1989. PMID: 2556504

6

Chronic progressive external ophthalmoplegia with ragged-red fibers: clinical, morphological and genetic investigations in 43 patients.

Laforêt P, Lombès A, Eymard B, Danan C, Chevallay M, Rouche A, Frachon P, Fardeau M. Laforêt P, et al. Among authors: eymard b. Neuromuscul Disord. 1995 Sep;5(5):399-413. doi: 10.1016/0960-8966(94)00080-s. Neuromuscul Disord. 1995. PMID: 7496174

7

Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy.

Eymard B, Romero NB, Leturcq F, Piccolo F, Carrié A, Jeanpierre M, Collin H, Deburgrave N, Azibi K, Chaouch M, Merlini L, Thémar-Noël C, Penisson I, Mayer M, Tanguy O, Campbell KP, Kaplan JC, Tomé FM, Fardeau M. Eymard B, et al. Neurology. 1997 May;48(5):1227-34. doi: 10.1212/wnl.48.5.1227. Neurology. 1997. PMID: 9153448

8

[Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies].

Laforêt P, Eymard B, Danan C, Chevallay M, Rouche A, Frachon P, Fardeau M, Lombès A. Laforêt P, et al. Among authors: eymard b. Rev Neurol (Paris). 1997 Feb;153(1):51-8. Rev Neurol (Paris). 1997. PMID: 9296156 French.

9

Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophy.

Laforêt P, de Toma C, Eymard B, Becane HM, Jeanpierre M, Fardeau M, Duboc D. Laforêt P, et al. Among authors: eymard b. Neurology. 1998 Nov;51(5):1454-6. doi: 10.1212/wnl.51.5.1454. Neurology. 1998. PMID: 9818880

10

[Miyoshi distal myopathy: specific signs and incidence].

Eymard B, Laforêt P, Tomé FM, Collin H, Leroy JP, Hauw JJ, Richard I, Beckmann J, Fardeau M. Eymard B, et al. Rev Neurol (Paris). 2000 Feb;156(2):161-8. Rev Neurol (Paris). 2000. PMID: 10743015 French.

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