Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: potential role in reinnervation ability and disease progression von BRUNETEAU, Gaëlle, SIMONET, Thomas, HELL-REMY, Caroline, SALACHAS, François, PRADAT, Pierre-François, FOURNIER, Emmanuel, LACOMBLEZ, Lucette, KOENIG, Jeanine, ROMERO, Norma Beatriz, FONTAINE, Bertrand, MEININGER, Vincent, SCHAEFFER, Laurent, BAUCHE, Stéphanie, HANTAÏ, Daniel, MANDJEE, Nathalie, MALFATTI, Edoardo, GIRARD, Emmanuelle, TANGUY, Marie-Laure, BEHIN, Anthony, KHIAMI, Frédéric, SARIALI, Elhadi

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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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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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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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Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function von Huzé, Caroline, Bauché, Stéphanie, Richard, Pascale, Chevessier, Frédéric, Goillot, Evelyne, Gaudon, Karen, Ben Ammar, Asma, Chaboud, Annie, Grosjean, Isabelle, Lecuyer, Heba-Aude, Bernard, Véronique, Rouche, Andrée, Alexandri, Nektaria, Kuntzer, Thierry, Fardeau, Michel, Fournier, Emmanuel, Brancaccio, Andrea, Rüegg, Markus A., Koenig, Jeanine, Eymard, Bruno, Schaeffer, Laurent, Hantaï, Daniel

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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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Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy von Bauché, Stéphanie, Vellieux, Geoffroy, Sternberg, Damien, Fontenille, Marie-Joséphine, De Bruyckere, Elodie, Davoine, Claire-Sophie, Brochier, Guy, Messéant, Julien, Wolf, Lucie, Fardeau, Michel, Lacène, Emmanuelle, Romero, Norma, Koenig, Jeanine, Fournier, Emmanuel, Hantaï, Daniel, Streichenberger, Nathalie, Manel, Veronique, Lacour, Arnaud, Nadaj-Pakleza, Aleksandra, Sukno, Sylvie, Bouhour, Françoise, Laforêt, Pascal, Fontaine, Bertrand, Strochlic, Laure, Eymard, Bruno, Chevessier, Frédéric, Stojkovic, Tanya, Nicole, Sophie

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A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctions von Chevessier, Frédéric, Girard, Emmanuelle, Molgó, Jordi, Bartling, Sönke, Koenig, Jeanine, Hantaï, Daniel, Witzemann, Veit

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Congenital myasthenic syndromes von Hantaï, Daniel, Richard, Pascale, Koenig, Jeanine, Eymard, Bruno

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Endplate denervation correlates with Nogo‐A muscle expression in amyotrophic lateral sclerosis patients von Bruneteau, Gaëlle, Bauché, Stéphanie, Gonzalez de Aguilar, Jose Luis, Brochier, Guy, Mandjee, Nathalie, Tanguy, Marie‐Laure, Hussain, Ghulam, Behin, Anthony, Khiami, Frédéric, Sariali, Elhadi, Hell‐Remy, Caroline, Salachas, François, Pradat, Pierre‐François, Lacomblez, Lucette, Nicole, Sophie, Fontaine, Bertrand, Fardeau, Michel, Loeffler, Jean‐Philippe, Meininger, Vincent, Fournier, Emmanuel, Koenig, Jeanine, Hantaï, Daniel

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Peripheral nerve hyperexcitability with preterminal nerve and neuromuscular junction remodeling is a hallmark of Schwartz-Jampel syndrome von Bauché, Stéphanie, Boerio, Delphine, Davoine, Claire-Sophie, Bernard, Véronique, Stum, Morgane, Bureau, Cécile, Fardeau, Michel, Romero, Norma Beatriz, Fontaine, Bertrand, Koenig, Jeanine, Hantaï, Daniel, Gueguen, Antoine, Fournier, Emmanuel, Eymard, Bruno, Nicole, Sophie

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Immunocytochemical characterization of a new marker of fibrous and reactive astrocytes von Ridet, Jean-Luc, Alonso, Gérard, Chauvet, Norbert, Chapron, Jacqueline, Koenig, Jeanine, Privat, Alain

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Corrigendum to ‘Peripheral nerve hyperexcitability with preterminal nerve and neuromuscular junction remodeling is a hallmark of Schwartz-Jampel syndrome’ [Neuromuscul Disord 23 (2... von Bauché, Stéphanie, Boerio, Delphine, Davoine, Claire-Sophie, Bernard, Véronique, Stum, Morgane, Bureau, Cécile, Fardeau, Michel, Romero, Norma Beatriz, Fontaine, Bertrand, Koenig, Jeanine, Hantaï, Daniel, Gueguen, Antoine, Fournier, Emmanuel, Eymard, Bruno, Nicole, Sophie

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Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function von Huzé, Caroline, Bauché, Stéphanie, Richard, Pascale, Chevessier, Frédéric, Goillot, Evelyne, Gaudon, Karen, Ben Ammar, Asma, Chaboud, Annie, Grosjean, Isabelle, Lecuyer, Heba-Aude, Bernard, Véronique, Rouche, Andrée, Alexandri, Nektaria, Kuntzer, Thierry, Fardeau, Michel, Fournier, Emmanuel, Brancaccio, Andrea, Rüegg, Markus A., Koenig, Jeanine, Eymard, Bruno, Schaeffer, Laurent, Hantaï, Daniel

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A synonymous CHRNE mutation responsible for an aberrant splicing leading to congenital myasthenic syndrome von Richard, Pascale, Gaudon, Karen, Fournier, Emmanuel, Jackson, Christopher, Bauché, Stéphanie, Haddad, Hafedh, Koenig, Jeanine, Echenne, Bernard, Hantaï, Daniel, Eymard, Bruno

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

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Thrombin reduces MuSK and acetylcholine receptor expression along with neuromuscular contact size in vitro von Faraut, Brice, Ravel-Chapuis, Aymeric, Bonavaud, Sylvie, Jandrot-Perrus, Martine, Verdière-Sahuqué, Martine, Schaeffer, Laurent, Koenig, Jeanine, Hantaï, Daniel

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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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Congenital myasthenic syndrome caused by decreased receptor channel openings due to a novel mutation in the nAChR ε-subunit von Yu, Hua, Ishigaki, Keiko, Shimahara, Takeshi, Bournaud, Roland, Poupon, Chantal Le, de Carvalho, Lia Prado, Corringer, Pierre Jean, Koenig, Jeanine, Eymard, Bruno, Hantaï, Daniel

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