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N Tabti

Showing results (11-20 of 21) with videos related to

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Neurology|September 25, 2003
Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysisD Sternberg, N Tabti, E Fournier, et al.
Acta Physiologica Scandinavica|November 1, 1986
Pharmacological characterization of the calcium-insensitive, intermittent acetylcholine release at the rat neuromuscular junctionN Tabti, M T Lupa, S P Yu, et al.
The Journal of Physiology|May 23, 1998
Functional expression of the Ile693Thr Na+ channel mutation associated with paramyotonia congenita in a human cell lineE Plassart-Schiess, L Lhuillier, A L George, et al.
Neuroscience|January 1, 1990
Terminal sprouting in mouse neuromuscular junctions poisoned with botulinum type A toxin: morphological and electrophysiological featuresD Angaut-Petit, J Molgó, J X Comella, et al.
The Journal of Physiology|December 1, 1986
The nature and origin of calcium-insensitive miniature end-plate potentials at rodent neuromuscular junctionsM T Lupa, N Tabti, S Thesleff, et al.
The Journal of Physiology|May 1, 1992
Pulsatile release of acetylcholine by nerve terminals (synaptosomes) isolated from Torpedo electric organR Girod, L Eder-Colli, J Medilanski, et al.
La Nouvelle Presse Medicale|November 20, 1982
[Detection of peripheral diabetic neuropathy. A reappraisal of electrophysiological data]M Rieu, A Sebille, F Perrier, et al.
Kidney International|January 1, 1996
Periodic paralysis and voltage-gated ion channelsB Fontaine, P Lapie, E Plassart, et al.
Journal De Physiologie|January 1, 1990
Presynaptic actions of botulinal neurotoxins at vertebrate neuromuscular junctionsJ Molgo, J X Comella, D Angaut-Petit, et al.
Brain : a Journal of Neurology|May 17, 2001
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4AD Sternberg, T Maisonobe, K Jurkat-Rott, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Neurology|September 25, 2003
Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysisD Sternberg, N Tabti, E Fournier, et al.
Acta Physiologica Scandinavica|November 1, 1986
Pharmacological characterization of the calcium-insensitive, intermittent acetylcholine release at the rat neuromuscular junctionN Tabti, M T Lupa, S P Yu, et al.
The Journal of Physiology|May 23, 1998
Functional expression of the Ile693Thr Na+ channel mutation associated with paramyotonia congenita in a human cell lineE Plassart-Schiess, L Lhuillier, A L George, et al.
Neuroscience|January 1, 1990
Terminal sprouting in mouse neuromuscular junctions poisoned with botulinum type A toxin: morphological and electrophysiological featuresD Angaut-Petit, J Molgó, J X Comella, et al.
The Journal of Physiology|December 1, 1986
The nature and origin of calcium-insensitive miniature end-plate potentials at rodent neuromuscular junctionsM T Lupa, N Tabti, S Thesleff, et al.
The Journal of Physiology|May 1, 1992
Pulsatile release of acetylcholine by nerve terminals (synaptosomes) isolated from Torpedo electric organR Girod, L Eder-Colli, J Medilanski, et al.
La Nouvelle Presse Medicale|November 20, 1982
[Detection of peripheral diabetic neuropathy. A reappraisal of electrophysiological data]M Rieu, A Sebille, F Perrier, et al.
Kidney International|January 1, 1996
Periodic paralysis and voltage-gated ion channelsB Fontaine, P Lapie, E Plassart, et al.
Journal De Physiologie|January 1, 1990
Presynaptic actions of botulinal neurotoxins at vertebrate neuromuscular junctionsJ Molgo, J X Comella, D Angaut-Petit, et al.
Brain : a Journal of Neurology|May 17, 2001
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4AD Sternberg, T Maisonobe, K Jurkat-Rott, et al.
Pageof 3