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B Eymard

Showing results (71-80 of 160) with videos related to

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Neurology|December 15, 2004
New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysisS Vicart, D Sternberg, E Fournier, et al.
Arthritis and Rheumatism|February 13, 2002
Results and long-term followup of intravenous immunoglobulin infusions in chronic, refractory polymyositis: an open study with thirty-five adult patientsPatrick Cherin, S Pelletier, A Teixeira, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1993
[Cardiac involvement in certain muscular diseases. Apropos of 216 cases]J Monségu, D Duboc, L Freychet, et al.
The Journal of Clinical Investigation|November 15, 1996
Association of arthrogryposis multiplex congenita with maternal antibodies inhibiting fetal acetylcholine receptor functionS Riemersma, A Vincent, D Beeson, et al.
Revue Neurologique|March 1, 1997
[Juvenile GM2 gangliosidosis with progressive spinal muscular atrophy onset]P Rondot, R Navon, B Eymard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 2, 2015
[Congenital myasthenic syndromes in childhood: Drug therapeutic strategies]S de la Vaissière, A Toutain, M-A Chêne, et al.
Arthritis and Rheumatism|July 21, 2000
Gallium-67 scintigraphy in macrophagic myofasciitisP Chérin, F J Authier, R K Gherardi, et al.
Neurology|February 24, 2010
Cardiac involvement is frequent in patients with the m.8344A>G mutation of mitochondrial DNAK Wahbi, S Larue, C Jardel, et al.
Revue Neurologique|July 14, 2009
[Multiple acyl-CoA dehydrogenase deficiency (MADD): a curable cause of genetic muscular lipidosis]E Maillart, C Acquaviva-Bourdain, O Rigal, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 1, 2007
[Early detection of myocardial disease in young patients with Becker's muscular dystrophy asymptomatic from the cardiac point of view: value of myocardial doppler tissue imaging]C Meune, K Wahbi, H M Bécane, et al.
Pageof 16

Showing results (71-80 of 160) with videos related to

Sort By:
Pageof 16
Neurology|December 15, 2004
New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysisS Vicart, D Sternberg, E Fournier, et al.
Arthritis and Rheumatism|February 13, 2002
Results and long-term followup of intravenous immunoglobulin infusions in chronic, refractory polymyositis: an open study with thirty-five adult patientsPatrick Cherin, S Pelletier, A Teixeira, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1993
[Cardiac involvement in certain muscular diseases. Apropos of 216 cases]J Monségu, D Duboc, L Freychet, et al.
The Journal of Clinical Investigation|November 15, 1996
Association of arthrogryposis multiplex congenita with maternal antibodies inhibiting fetal acetylcholine receptor functionS Riemersma, A Vincent, D Beeson, et al.
Revue Neurologique|March 1, 1997
[Juvenile GM2 gangliosidosis with progressive spinal muscular atrophy onset]P Rondot, R Navon, B Eymard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 2, 2015
[Congenital myasthenic syndromes in childhood: Drug therapeutic strategies]S de la Vaissière, A Toutain, M-A Chêne, et al.
Arthritis and Rheumatism|July 21, 2000
Gallium-67 scintigraphy in macrophagic myofasciitisP Chérin, F J Authier, R K Gherardi, et al.
Neurology|February 24, 2010
Cardiac involvement is frequent in patients with the m.8344A>G mutation of mitochondrial DNAK Wahbi, S Larue, C Jardel, et al.
Revue Neurologique|July 14, 2009
[Multiple acyl-CoA dehydrogenase deficiency (MADD): a curable cause of genetic muscular lipidosis]E Maillart, C Acquaviva-Bourdain, O Rigal, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 1, 2007
[Early detection of myocardial disease in young patients with Becker's muscular dystrophy asymptomatic from the cardiac point of view: value of myocardial doppler tissue imaging]C Meune, K Wahbi, H M Bécane, et al.
Pageof 16