Eymard B - Search Results

1

MUSK, a new target for mutations causing congenital myasthenic syndrome.

Chevessier F, Faraut B, Ravel-Chapuis A, Richard P, Gaudon K, Bauché S, Prioleau C, Herbst R, Goillot E, Ioos C, Azulay JP, Attarian S, Leroy JP, Fournier E, Legay C, Schaeffer L, Koenig J, Fardeau M, Eymard B, Pouget J, Hantaï D. Chevessier F, et al. Among authors: eymard b. Hum Mol Genet. 2004 Dec 15;13(24):3229-40. doi: 10.1093/hmg/ddh333. Epub 2004 Oct 20. Hum Mol Genet. 2004. PMID: 15496425

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

Effect of myasthenic patient sera on the number and distribution of acetylcholine receptors in muscle and nerve-muscle cultures from rat. Correlations with clinical state.

Eymard B, de la Porte S, Pannier C, Berrih-Aknin S, Morel E, Fardeau M, Bach JF, Koenig J. Eymard B, et al. J Neurol Sci. 1988 Aug;86(1):41-59. doi: 10.1016/0022-510x(88)90006-8. J Neurol Sci. 1988. PMID: 3171596

5

X-linked vacuolated myopathy: complement membrane attack complex on surface membrane of injured muscle fibers.

Villanova M, Louboutin JP, Chateau D, Eymard B, Sagniez M, Tomé FM, Fardeau M. Villanova M, et al. Among authors: eymard b. Ann Neurol. 1995 May;37(5):637-45. doi: 10.1002/ana.410370514. Ann Neurol. 1995. PMID: 7755359

6

Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations.

Plassart E, Reboul J, Rime CS, Recan D, Millasseau P, Eymard B, Pelletier J, Thomas C, Chapon F, Desnuelle C, et al. Plassart E, et al. Among authors: eymard b. Eur J Hum Genet. 1994;2(2):110-24. doi: 10.1159/000472351. Eur J Hum Genet. 1994. PMID: 8044656

7

Late-onset rod myopathy associated with monoclonal gammopathy.

Eymard B, Brouet JC, Collin H, Chevallay M, Bussel A, Fardeau M. Eymard B, et al. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):557-60. doi: 10.1016/0960-8966(93)90115-z. Neuromuscul Disord. 1993. PMID: 8186711

8

Effect of sera from myasthenia gravis patients and of alpha-bungarotoxin on acetylcholinesterase during in vitro neuromuscular synaptogenesis.

de la Porte S, Ragueh F, Eymard B, Courbin P, Chapron J, Koenig J. de la Porte S, et al. Among authors: eymard b. J Neurol Sci. 1993 Jul;117(1-2):92-102. doi: 10.1016/0022-510x(93)90160-z. J Neurol Sci. 1993. PMID: 8410074

9

Paramyotonia congenita: genotype to phenotype correlations in two families and report of a new mutation in the sodium channel gene.

Plassart E, Eymard B, Maurs L, Hauw JJ, Lyon-Caen O, Fardeau M, Fontaine B. Plassart E, et al. Among authors: eymard b. J Neurol Sci. 1996 Oct;142(1-2):126-33. doi: 10.1016/0022-510x(96)00173-6. J Neurol Sci. 1996. PMID: 8902732

10

Chromosome 15-linked limb-girdle muscular dystrophy: clinical phenotypes in Reunion Island and French metropolitan communities.

Fardeau M, Eymard B, Mignard C, Tomé FM, Richard I, Beckmann JS. Fardeau M, et al. Among authors: eymard b. Neuromuscul Disord. 1996 Dec;6(6):447-53. doi: 10.1016/s0960-8966(96)00387-2. Neuromuscul Disord. 1996. PMID: 9027854

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