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B Bady

Showing results (61-70 of 65) with videos related to

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Neurophysiologie Clinique = Clinical Neurophysiology|March 1, 1992
[Electrophysiologic data on myasthenic syndromes of the Lambert-Eaton type. A series of 23 cases]B Bady, A Truffert, M Brechard, et al.
Acta Neurologica Scandinavica|October 1, 1995
DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutationsP M Gonnaud, F Sturtz, Y Fourbil, et al.
European Neurology|January 1, 1996
Modelization of motor nerve conduction velocities for Charcot-Marie-Tooth (Type-1) patients. CMT-France NetworkF G Sturtz, F Chauvin, E Ollagnon-Roman, et al.
American Journal of Human Genetics|February 1, 1995
Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian familiesA Elbaz, J Vale-Santos, K Jurkat-Rott, et al.
American Journal of Human Genetics|May 1, 1997
Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical originsI Richard, L Brenguier, P Dinçer, et al.
Pageof 7

Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
Neurophysiologie Clinique = Clinical Neurophysiology|March 1, 1992
[Electrophysiologic data on myasthenic syndromes of the Lambert-Eaton type. A series of 23 cases]B Bady, A Truffert, M Brechard, et al.
Acta Neurologica Scandinavica|October 1, 1995
DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutationsP M Gonnaud, F Sturtz, Y Fourbil, et al.
European Neurology|January 1, 1996
Modelization of motor nerve conduction velocities for Charcot-Marie-Tooth (Type-1) patients. CMT-France NetworkF G Sturtz, F Chauvin, E Ollagnon-Roman, et al.
American Journal of Human Genetics|February 1, 1995
Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian familiesA Elbaz, J Vale-Santos, K Jurkat-Rott, et al.
American Journal of Human Genetics|May 1, 1997
Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical originsI Richard, L Brenguier, P Dinçer, et al.
Pageof 7