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B Eymard

Showing results (101-110 of 160) with videos related to

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Archives of Neurology|June 19, 2001
Anti-titin antibodies in myasthenia gravis: tight association with thymoma and heterogeneity of nonthymoma patientsA M Yamamoto, P Gajdos, B Eymard, et al.
Revue Neurologique|May 5, 2019
Life-threatening lactic acidosis occurring in adults with mitochondrial disordersM Brisset, A Béhin, C Pottier, et al.
American Journal of Human Genetics|October 3, 1998
Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic)C Donger, E Krejci, A P Serradell, et al.
Circulation|March 2, 1999
Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophyA Lazarus, J Varin, Z Ounnoughene, et al.
Neurology|January 1, 1997
The fetal/adult acetylcholine receptor antibody ratio in mothers with myasthenia gravis as a marker for transfer of the disease to the newbornM Gardnerova, B Eymard, E Morel, et al.
The Journal of Clinical Investigation|August 1, 1994
Association of neonatal myasthenia gravis with antibodies against the fetal acetylcholine receptorB Vernet-der Garabedian, M Lacokova, B Eymard, et al.
AJNR. American Journal of Neuroradiology|February 12, 2021
Fast Stent Retrieval during Mechanical Thrombectomy Improves Recanalization in Patients with the Negative Susceptibility Vessel SignS Soize, J-B Eymard, S Cheikh-Rouhou, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 19, 2009
Late-onset cervicoscapular muscle atrophy and weakness after radiotherapy for Hodgkin disease: a case seriesA Furby, A Béhin, J-P Lefaucheur, et al.
Neuromuscular Disorders : NMD|November 18, 2011
Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutationsI Wargon, P Richard, T Kuntzer, et al.
Presse Medicale (Paris, France : 1983)|March 8, 2000
[Macrophagic myofasciitis. Study and Research Group on Acquired and Dysimmunity-related muscular diseases (GERMMAD)]P Chérin, P Laforêt, R K Ghérardi, et al.
Pageof 16

Showing results (101-110 of 160) with videos related to

Sort By:
Pageof 16
Archives of Neurology|June 19, 2001
Anti-titin antibodies in myasthenia gravis: tight association with thymoma and heterogeneity of nonthymoma patientsA M Yamamoto, P Gajdos, B Eymard, et al.
Revue Neurologique|May 5, 2019
Life-threatening lactic acidosis occurring in adults with mitochondrial disordersM Brisset, A Béhin, C Pottier, et al.
American Journal of Human Genetics|October 3, 1998
Mutation in the human acetylcholinesterase-associated collagen gene, COLQ, is responsible for congenital myasthenic syndrome with end-plate acetylcholinesterase deficiency (Type Ic)C Donger, E Krejci, A P Serradell, et al.
Circulation|March 2, 1999
Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophyA Lazarus, J Varin, Z Ounnoughene, et al.
Neurology|January 1, 1997
The fetal/adult acetylcholine receptor antibody ratio in mothers with myasthenia gravis as a marker for transfer of the disease to the newbornM Gardnerova, B Eymard, E Morel, et al.
The Journal of Clinical Investigation|August 1, 1994
Association of neonatal myasthenia gravis with antibodies against the fetal acetylcholine receptorB Vernet-der Garabedian, M Lacokova, B Eymard, et al.
AJNR. American Journal of Neuroradiology|February 12, 2021
Fast Stent Retrieval during Mechanical Thrombectomy Improves Recanalization in Patients with the Negative Susceptibility Vessel SignS Soize, J-B Eymard, S Cheikh-Rouhou, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 19, 2009
Late-onset cervicoscapular muscle atrophy and weakness after radiotherapy for Hodgkin disease: a case seriesA Furby, A Béhin, J-P Lefaucheur, et al.
Neuromuscular Disorders : NMD|November 18, 2011
Long-term follow-up of patients with congenital myasthenic syndrome caused by COLQ mutationsI Wargon, P Richard, T Kuntzer, et al.
Presse Medicale (Paris, France : 1983)|March 8, 2000
[Macrophagic myofasciitis. Study and Research Group on Acquired and Dysimmunity-related muscular diseases (GERMMAD)]P Chérin, P Laforêt, R K Ghérardi, et al.
Pageof 16