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B Eymard

Showing results (51-60 of 160) with videos related to

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Journal of Autoimmunity|April 1, 1991
Anti-acetylcholine receptor antibodies in neonatal myasthenia gravis: heterogeneity and pathogenic significanceB Eymard, B Vernet-der Garabedian, S Berrih-Aknin, et al.
Journal of the Neurological Sciences|October 1, 1996
Paramyotonia congenita: genotype to phenotype correlations in two families and report of a new mutation in the sodium channel geneE Plassart, B Eymard, L Maurs, et al.
Revue Neurologique|February 1, 1997
[Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies]P Laforêt, B Eymard, C Danan, et al.
Neuromuscular Disorders : NMD|September 1, 1995
Chronic progressive external ophthalmoplegia with ragged-red fibers: clinical, morphological and genetic investigations in 43 patientsP Laforêt, A Lombès, B Eymard, et al.
Neurology|November 18, 1998
Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophyP Laforêt, C de Toma, B Eymard, et al.
Journal of the Neurological Sciences|October 1, 1992
Combined effects of a thymic peptide, thymopoietin and myasthenic patient sera in rat myotube cultureB Eymard, C Aimé, C Cottin, et al.
Neurology|November 9, 2000
Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotype correlationP Laforêt, M Nicolino, P B Eymard, et al.
Revue Neurologique|January 5, 2001
["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data]P Laforêt, F Ziegler, D Sternberg, et al.
Revue Neurologique|January 1, 1993
[Paraneoplastic myasthenic syndrome]J M Léger, A C Bachoud-Lévi, B Eymard, et al.
Annals of Neurology|May 1, 1995
X-linked vacuolated myopathy: complement membrane attack complex on surface membrane of injured muscle fibersM Villanova, J P Louboutin, D Chateau, et al.
Pageof 16

Showing results (51-60 of 160) with videos related to

Sort By:
Pageof 16
Journal of Autoimmunity|April 1, 1991
Anti-acetylcholine receptor antibodies in neonatal myasthenia gravis: heterogeneity and pathogenic significanceB Eymard, B Vernet-der Garabedian, S Berrih-Aknin, et al.
Journal of the Neurological Sciences|October 1, 1996
Paramyotonia congenita: genotype to phenotype correlations in two families and report of a new mutation in the sodium channel geneE Plassart, B Eymard, L Maurs, et al.
Revue Neurologique|February 1, 1997
[Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies]P Laforêt, B Eymard, C Danan, et al.
Neuromuscular Disorders : NMD|September 1, 1995
Chronic progressive external ophthalmoplegia with ragged-red fibers: clinical, morphological and genetic investigations in 43 patientsP Laforêt, A Lombès, B Eymard, et al.
Neurology|November 18, 1998
Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophyP Laforêt, C de Toma, B Eymard, et al.
Journal of the Neurological Sciences|October 1, 1992
Combined effects of a thymic peptide, thymopoietin and myasthenic patient sera in rat myotube cultureB Eymard, C Aimé, C Cottin, et al.
Neurology|November 9, 2000
Juvenile and adult-onset acid maltase deficiency in France: genotype-phenotype correlationP Laforêt, M Nicolino, P B Eymard, et al.
Revue Neurologique|January 5, 2001
["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data]P Laforêt, F Ziegler, D Sternberg, et al.
Revue Neurologique|January 1, 1993
[Paraneoplastic myasthenic syndrome]J M Léger, A C Bachoud-Lévi, B Eymard, et al.
Annals of Neurology|May 1, 1995
X-linked vacuolated myopathy: complement membrane attack complex on surface membrane of injured muscle fibersM Villanova, J P Louboutin, D Chateau, et al.
Pageof 16