A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia von Ben Ammar, Asma, Soltanzadeh, Payam, Bauché, Stéphanie, Richard, Pascale, Goillot, Evelyne, Herbst, Ruth, Gaudon, Karen, Huzé, Caroline, Schaeffer, Laurent, Yamanashi, Yuji, Higuchi, Osamu, Taly, Antoine, Koenig, Jeanine, Leroy, Jean-Paul, Hentati, Fayçal, Najmabadi, Hossein, Kahrizi, Kimia, Ilkhani, Manouchehr, Fardeau, Michel, Eymard, Bruno, Hantaï, Daniel

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MUSK, a new target for mutations causing congenital myasthenic syndrome von Chevessier, Frédéric, Faraut, Brice, Ravel-Chapuis, Aymeric, Richard, Pascale, Gaudon, Karen, Bauché, Stéphanie, Prioleau, Cassandra, Herbst, Ruth, Goillot, Evelyne, Ioos, Christine, Azulay, Jean-Philippe, Attarian, Shahram, Leroy, Jean-Paul, Fournier, Emmanuel, Legay, Claire, Schaeffer, Laurent, Koenig, Jeanine, Fardeau, Michel, Eymard, Bruno, Pouget, Jean, Hantaï, Daniel

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Mutations of the Selenoprotein N Gene, Which Is Implicated in Rigid Spine Muscular Dystrophy, Cause the Classical Phenotype of Multiminicore Disease: Reassessing the Nosology of Ea... von Ferreiro, Ana, Quijano-Roy, Susana, Pichereau, Claire, Moghadaszadeh, Behzad, Goemans, Nathalie, Bönnemann, Carsten, Jungbluth, Heinz, Straub, Volker, Villanova, Marcello, Leroy, Jean-Paul, Romero, Norma B., Martin, Jean-Jacques, Muntoni, Francesco, Voit, Thomas, Estournet, Brigitte, Richard, Pascale, Fardeau, Michel, Guicheney, Pascale

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The origin of tubular aggregates in human myopathies von Chevessier, Frédéric, Bauché-Godard, Stéphanie, Leroy, Jean-Paul, Koenig, Jeanine, Paturneau-Jouas, Marion, Eymard, Bruno, Hantaï, Daniel, Verdière-Sahuqué, Martine

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A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene von Ferreiro, Ana, Monnier, Nicole, Romero, Norma B., Leroy, Jean-Paul, Bönnemann, Carsten, Haenggeli, Charles-Antoine, Straub, Volker, Voss, Wolfgang D., Nivoche, Yves, Jungbluth, Heinz, Lemainque, Arnaud, Voit, Thomas, Lunardi, Joël, Fardeau, Michel, Guicheney, Pascale

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Correction: A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia von Ben Ammar, Asma, Soltanzadeh, Payam, Bauché, Stéphanie, Richard, Pascale, Goillot, Evelyne, Herbst, Ruth, Gaudon, Karen, Huzé, Caroline, Schaeffer, Laurent, Yamanashi, Yuji, Higuchi, Osamu, Taly, Antoine, Koenig, Jeanine, Leroy, Jean-Paul, Hentati, Fayçal, Najmabadi, Hossein, Kahrizi, Kimia, Ilkhani, Manouchehr, Fardeau, Michel, Eymard, Bruno, Hantaï, Daniel

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Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation von Auré, Karine, Fayet, Guillemette, Leroy, Jean Paul, Lacène, Emmanuelle, Romero, Norma Beatriz, Lombès, Anne

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Two novel mutations in the COLQ gene cause endplate acetylcholinesterase deficiency von Ishigaki, Keiko, Nicolle, Delphine, Krejci, Eric, Leroy, Jean-Paul, Koenig, Jeanine, Fardeau, Michel, Eymard, Bruno, Hantaı̈, Daniel

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Aseptic Neutrophilic Abscess of the Vulva von Karam, Allan, Saliou, Anne-Helene, LeRoy, Jean-Paul, Misery, Laurent, Laurent, Yves

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Abnormal Distribution of Calcium-Handling Proteins: A Novel Distinctive Marker in Core Myopathies von Herasse, Muriel, Parain, Karine, Marty, Isabelle, Monnier, Nicole, Kaindl, Angela M, Leroy, Jean-Paul, Richard, Pascale, Lunardi, Jöel, Romero, Norma B, Ferreiro, Ana

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A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis von Laforêt, Pascal, Richard, Pascale, Said, Mina Ait, Romero, Norma Beatriz, Lacene, Emmanuelle, Leroy, Jean-Paul, Baussan, Christiane, Hogrel, Jean-Yves, Lavergne, Thomas, Wahbi, Karim, Hainque, Bernard, Duboc, Denis

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Phosphonocationic Lipids in Protein Delivery to Mice Lungs von Guillaume, Christine, Delépine, Pascal, Mercier, Bernard, Gobin, Eric, Leroy, Jean‐Paul, Morin, Vincent, Férec, Claude

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Modulation of Cardiovascular Functions by Angiotensin II within the Brainstem of Conscious Trout, Oncorhynchus mykiss von PAMANTUNG, TOMMY FERDINANDUS, LEROY, JEAN-PAUL, MABIN, DOMINIQUE, LE MEVEL, JEAN-CLAUDE

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Electrophysiological and morphological characterization of a case of autosomal recessive congenital myasthenic syndrome with acetylcholine receptor deficiency due to a N88K rapsyn... von Yasaki, Eriko, Prioleau, Cassandra, Barbier, Julien, Richard, Pascale, Andreux, Frédéric, Leroy, Jean-Paul, Dartevelle, Philippe, Koenig, Jeanine, Molgó, Jordi, Fardeau, Michel, Eymard, Bruno, Hantaı̈, Daniel

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Evaluation of muscle glycogen content by 13C NMR spectroscopy in adult-onset acid maltase deficiency von Wary, Claire, Laforêt, Pascal, Eymard, Bruno, Fardeau, Michel, Leroy-Willig, Anne, Bassez, Guillaume, Leroy, Jean-Paul, Caillaud, Catherine, Poenaru, Livia, Carlier, Pierre G

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The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease von Davignon, Laurianne, Chauveau, Claire, Julien, Cédric, Dill, Corinne, Duband-Goulet, Isabelle, Cabet, Eva, Buendia, Brigitte, Lilienbaum, Alain, Rendu, John, Minot, Marie Christine, Guichet, Agnès, Allamand, Valérie, Vadrot, Nathalie, Fauré, Julien, Odent, Sylvie, Lazaro, Leïla, Leroy, Jean Paul, Marcorelles, Pascale, Dubourg, Odile, Ferreiro, Ana

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Cationic phosphonolipids as nonviral gene transfer agents in the lungs of mice von Guillaume-Gable, C, Floch, V, Mercier, B, Audrézet, M P, Gobin, E, Le Bolch, G, Yaouanc, J J, Clément, J C, des Abbayes, H, Leroy, J P, Morin, V, Férec, C

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Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesia von Romero, Norma Beatriz, Monnier, Nicole, Viollet, Louis, Cortey, Anne, Chevallay, Martine, Leroy, Jean Paul, Lunardi, Joël, Fardeau, Michel

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Role of dorsal vagal motor nucleus in angiotensin II-mediated tachycardia in the conscious trout Oncorhynchus mykiss von Pamantung, Tommy Ferdinandus, Leroy, Jean-Paul, Mabin, Dominique, Le Mével, Jean-Claude

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The binding of some human antiendothelial cell antibodies induces endothelial cell apoptosis von Bordron, A, Dueymes, M, Levy, Y, Jamin, C, Leroy, J P, Piette, J C, Shoenfeld, Y, Youinou, P Y

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