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Genes and Immunity
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January 22, 2004
Association of the gene encoding the delta-subunit of the muscle acetylcholine receptor (CHRND) with acquired autoimmune myasthenia gravis
M Giraud, B Eymard, C Tranchant, et al.
Journal of Neuroimmunology
|
January 1, 1989
Alpha-bungarotoxin blocking antibodies in neonatal myasthenia gravis: frequency and selectivity
B Vernet-der Garabedian, B Eymard, J F Bach, et al.
Neuromuscular Disorders : NMD
|
December 10, 1997
Genealogical study of oculopharyngeal muscular dystrophy in France
G Brunet, F M Tomé, B Eymard, et al.
Magnetic Resonance Imaging
|
January 1, 1996
MR quantification of muscle fatty replacement in McArdle's disease
E De Kerviler, A Leroy-Willig, D Duboc, et al.
Revue Neurologique
|
January 1, 1990
[Communicating hydrocephalus disclosing neurosyphilis]
C Lamy, B Eymard, J M Léger, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation
|
July 9, 2002
Successful bridge to transplantation in a patient with Becker muscular dystrophy-associated cardiomyopathy
P Leprince, F Heloire, B Eymard, et al.
Revue Neurologique
|
October 8, 2024
Congenital myasthenic syndromes by Epsilon subunit mutations: Phenotypic profiles of 17 Algerian families
M I Kediha, M Tazir, D Sternberg, et al.
Clinical and Experimental Immunology
|
June 1, 1990
Neonatal myasthenia gravis: antigenic specificities of antibodies in sera from mothers and their infants
S J Tzartos, A Efthimiadis, E Morel, et al.
Genes and Immunity
|
June 18, 2004
Genetic control of autoantibody expression in autoimmune myasthenia gravis: role of the self-antigen and of HLA-linked loci
M Giraud, G Beaurain, B Eymard, et al.
Neuromuscular Disorders : NMD
|
November 25, 2022
Highly asymmetrical distribution of muscle wasting correlates to the heteroplasmy in a patient carrying a large-scale mitochondrial DNA deletion: a novel pathophysiological mechanism for explaining asymmetry in mitochondrial myopathies
M Masingue, B Rucheton, C Bris, et al.
Page
of 16
Search research articles
Search
Showing results (21-30 of 160) with videos related to
Sort By:
Page
of 16
Genes and Immunity
|
January 22, 2004
Association of the gene encoding the delta-subunit of the muscle acetylcholine receptor (CHRND) with acquired autoimmune myasthenia gravis
M Giraud, B Eymard, C Tranchant, et al.
Journal of Neuroimmunology
|
January 1, 1989
Alpha-bungarotoxin blocking antibodies in neonatal myasthenia gravis: frequency and selectivity
B Vernet-der Garabedian, B Eymard, J F Bach, et al.
Neuromuscular Disorders : NMD
|
December 10, 1997
Genealogical study of oculopharyngeal muscular dystrophy in France
G Brunet, F M Tomé, B Eymard, et al.
Magnetic Resonance Imaging
|
January 1, 1996
MR quantification of muscle fatty replacement in McArdle's disease
E De Kerviler, A Leroy-Willig, D Duboc, et al.
Revue Neurologique
|
January 1, 1990
[Communicating hydrocephalus disclosing neurosyphilis]
C Lamy, B Eymard, J M Léger, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation
|
July 9, 2002
Successful bridge to transplantation in a patient with Becker muscular dystrophy-associated cardiomyopathy
P Leprince, F Heloire, B Eymard, et al.
Revue Neurologique
|
October 8, 2024
Congenital myasthenic syndromes by Epsilon subunit mutations: Phenotypic profiles of 17 Algerian families
M I Kediha, M Tazir, D Sternberg, et al.
Clinical and Experimental Immunology
|
June 1, 1990
Neonatal myasthenia gravis: antigenic specificities of antibodies in sera from mothers and their infants
S J Tzartos, A Efthimiadis, E Morel, et al.
Genes and Immunity
|
June 18, 2004
Genetic control of autoantibody expression in autoimmune myasthenia gravis: role of the self-antigen and of HLA-linked loci
M Giraud, G Beaurain, B Eymard, et al.
Neuromuscular Disorders : NMD
|
November 25, 2022
Highly asymmetrical distribution of muscle wasting correlates to the heteroplasmy in a patient carrying a large-scale mitochondrial DNA deletion: a novel pathophysiological mechanism for explaining asymmetry in mitochondrial myopathies
M Masingue, B Rucheton, C Bris, et al.
Page
of 16