Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities von SEZNEC, Hervé, AGBULUT, Onnik, FOUQUET, Coralie, BUTLER-BROWNE, Gillian, DELACOURTE, André, JUNIEN, Claudine, GOURDON, Geneviève, SERGEANT, Nicolas, SAVOURET, Cédric, GHESTEM, Antoine, TABTI, Nacira, WILLER, Jean-Claude, OURTH, Lucie, DUROS, Chantal, BRISSON, Edith

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Composition of the Essential Oil of Leaves and Berries of Algerian Myrtle (Myrtus comunis L.) von Brada, M, Tabli, N, Boutopumi, H, Wathelet, Jean-Paul, Lognay, Georges

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Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysis von STERNBERG, D, TABTI, N, FOURNIER, E, HAINQUE, B, FONTAINE, B

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Electromyography guides toward subgroups of mutations in muscle channelopathies von Fournier, Emmanuel, Arzel, Marianne, Sternberg, Damien, Vicart, Savine, Laforet, Pascal, Eymard, Bruno, Willer, Jean-Claude, Tabti, Nacira, Fontaine, Bertrand

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Canaux ioniques et canalopathies : un lien entre molécules et grandes fonctions ? von Fontaine, B, Tabti, N

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Cold extends electromyography distinction between ion channel mutations causing myotonia von Fournier, Emmanuel, Viala, Karine, Gervais, Hélène, Sternberg, Damien, Arzel-Hézode, Marianne, Laforêt, Pascal, Eymard, Bruno, Tabti, Nacira, Willer, Jean-Claude, Vial, Christophe, Fontaine, Bertrand

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Unravelling the pathophysiology of calcium channel mutations causing neurological disorders von Fontaine, Bertrand, Tabti, Nacira

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Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A von Sternberg, Damien, Maisonobe, Thierry, Jurkat-Rott, Karin, Nicole, Sophie, Launay, Erika, Chauveau, Dominique, Tabti, Nacira, Lehmann-Horn, Frank, Hainque, Bernard, Fontaine, Bertrand

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Gravitational theories coupled to matter as invariant theories under Kac-Moody algebras von Tabti, N.

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Periodic paralysis and voltage-gated ion channels von Fontaine, Bertrand, Lapie, Pascale, Plassart, Emmanuelle, Tabti, Nacira, Nicole, Sophie, Reboul, Jocelyne, Rime-Davoine, Claire-Sophie

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Influence of muscle cells on the development of calcium currents in Xenopus spinal neurons von Lhuillier, L., Tabti, N.

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Terminal sprouting in mouse neuromuscular junctions poisoned with botulinum type a toxin: Morphological and electrophysiological features von Angaut-Petit, D., Molgó, J., Comella, J.X., Faille, L., Tabti, N.

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Functional characterization and cold sensitivity of T1313A, a new mutation of the skeletal muscle sodium channel causing paramyotonia congenita in humans von Bouhours, Magali, Sternberg, Damien, Davoine, Claire‐Sophie, Xavier, Ferrer, Willer, Jean Claude, Fontaine, Bertrand, Tabti, Nacira

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Characterization of surface roughness by EHD impedance von DESLOUIS, C, TABTI, N, TRIBOLLET, B

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A1152D mutation of the Na+ channel causes paramyotonia congenita and emphasizes the role of DIII/S4–S5 linker in fast inactivation von Bouhours, Magali, Luce, Sandrine, Sternberg, Damien, Willer, Jean Claude, Fontaine, Bertrand, Tabti, Nacira

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A study of synchronization of quantal transmitter release from mammalian motor endings by the use of botulinal toxins type A and D von Molgó, J, Siegel, L S, Tabti, N, Thesleff, S

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Three potassium currents in mouse motor nerve terminals von TABTI, N, BOURRET, C, MALLART, A

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Gating defects of a novel Na super(+) channel mutant causing hypokalemic periodic paralysis von Carle, T, Lhuillier, L, Luce, S, Sternberg, D, Devuyst, O, Fontaine, B, Tabti, N

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Pulsatile release of acetylcholine by nerve terminals (synaptosomes) isolated from Torpedo electric organ von Girod, R, Eder‐Colli, L, Medilanski, J, Dunant, Y, Tabti, N, Poo, M M

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The nature and origin of calcium-insensitive miniature end-plate potentials at rodent neuromuscular junctions von Lupa, M T, Tabti, N, Thesleff, S, Vyskocil, F, Yu, S P

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