Provisional practice recommendation for the management of myopathy in VCP‐associated multisystem proteinopathy von Roy, Bhaskar, Peck, Allison, Evangelista, Teresinha, Pfeffer, Gerald, Wang, Leo, Diaz‐Manera, Jordi, Korb, Manisha, Wicklund, Matthew P., Milone, Margherita, Freimer, Miriam, Kushlaf, Hani, Villar‐Quiles, Rocio‐Nur, Stojkovic, Tanya, Needham, Merrilee, Palmio, Johanna, Lloyd, Thomas E., Keung, Benison, Mozaffar, Tahseen, Weihl, Conrad Chris, Kimonis, Virginia

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Caveolinopathy: Clinical, histological, and muscle imaging features and follow‐up in a multicenter retrospective cohort von Berling, Edouard, Verebi, Camille, Venturelli, Nadia, Vassilopoulos, Stéphane, Béhin, Anthony, Tard, Céline, Michaud, Maud, Quiles, Rocio Nur Villar, Vicart, Savine, Masingue, Marion, Carlier, Robert‐Yves, Romero, Norma Beatriz, Lacene, Emmanuelle, Leturcq, France, Eymard, Bruno, Laforêt, Pascal, Stojkovic, Tanya

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SELENON (SEPN1) protects skeletal muscle from saturated fatty acid-induced ER stress and insulin resistance von Varone, Ersilia, Pozzer, Diego, Di Modica, Simona, Chernorudskiy, Alexander, Nogara, Leonardo, Baraldo, Martina, Cinquanta, Mario, Fumagalli, Stefano, Villar-Quiles, Rocio Nur, De Simoni, Maria-Grazia, Blaauw, Bert, Ferreiro, Ana, Zito, Ester

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Defective endoplasmic reticulum-mitochondria contacts and bioenergetics in SEPN1-related myopathy von Filipe, Anne, Chernorudskiy, Alexander, Arbogast, Sandrine, Varone, Ersilia, Villar-Quiles, Rocío-Nur, Pozzer, Diego, Moulin, Maryline, Fumagalli, Stefano, Cabet, Eva, Dudhal, Swati, De Simoni, Maria-Grazia, Denis, Raphaël, Vadrot, Nathalie, Dill, Corinne, Giovarelli, Matteo, Szweda, Luke, De Palma, Clara, Pinton, Paolo, Giorgi, Carlotta, Viscomi, Carlo, Clementi, Emilio, Missiroli, Sonia, Boncompagni, Simona, Zito, Ester, Ferreiro, Ana

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Phenotypical variability and atypical presentations in a French cohort of Andersen–Tawil syndrome von Villar‐Quiles, Rocio Nur, Sternberg, Damien, Tredez, Grégoire, Beatriz Romero, Norma, Evangelista, Teresinha, Lafôret, Pascal, Cintas, Pascal, Sole, Guilhem, Sacconi, Sabrina, Bendahhou, Said, Franques, Jérôme, Cances, Claude, Noury, JB, Delmont, Emilien, Blondy, Patricia, Perrin, Laurence, Hezode, Marianne, Fournier, Emmanuel, Fontaine, Bertrand, Stojkovic, Tanya, Vicart, Savine

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Inherited Defects of the ASC-1 Complex in Congenital Neuromuscular Diseases von Meunier, Justine, Villar-Quiles, Rocio-Nur, Duband-Goulet, Isabelle, Ferreiro, Ana

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Supratrochlear Neuralgia: A Prospective Case Series of 15 Patients von Pareja, Juan A., López‐Ruiz, Pedro, Mayo, Diego, Villar‐Quiles, Rocío‐Nur, Cárcamo, Alba, Gutiérrez‐Viedma, Álvaro, Lastarria, Carlo P., Romeral, María, Yangüela, Julio, Cuadrado, María‐Luz

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Confounding clinical presentation and different disease progression in CMT4B1 von Guimarães-Costa, Raquel, Villar-Quiles, Rocio-Nur, Latour, Philippe, Sole, Guilhem, Husson, Isabelle, Lacour, Arnaud, Leonard-Louis, Sarah, Stojkovic, Tanya

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Leukoencephalopathy and conduction blocks in PLEKHG5-associated intermediate CMT disease von Villar-Quiles, Rocio-Nur, Le, Van Thuy, Leonard-Louis, Sarah, Trang, Nguyen Thi, Huong, Nguyen Thi, Laddada, Lilia, Francou, Bruno, Maisonobe, Thierry, Azzedine, Hamid, Stojkovic, Tanya

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Improving Examination Skills in Neuromuscular Disorders Through an Educational Video von Villar‐Quiles, Rocio Nur, Bouaoud, Jebrane, Foy, Jean Philippe, Behin, Anthony, Masingue, Marion, Nguyen, Tan Mai, Iniesto, Miguel, Stojkovic, Tanya, Idbaih, Ahmed

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JAG2-related muscular dystrophy: When differential diagnosis matters von Nur Villar-Quiles, Rocio, Romero, Norma B, Tanya, Stojkovic

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Teaching NeuroImages: Adult-onset vanishing white matter disease von Villar-Quiles, Rocío-Nur, Delgado-Suárez, Celia, Jorquera-Moya, Manuela, Arpa-Gutiérrez, Javier, Ortega-Suero, Gloria

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A multicenter cross-sectional French study of the impact of COVID-19 on neuromuscular diseases von Pisella, Lucie Isoline, Fernandes, Sara, Solé, Guilhem, Stojkovic, Tanya, Tard, Céline, Chanson, Jean-Baptiste, Bouhour, Françoise, Salort-Campana, Emmanuelle, Beaudonnet, Guillemette, Debergé, Louise, Duval, Fanny, Grapperon, Aude-Marie, Masingue, Marion, Nadaj-Pakleza, Aleksandra, Péréon, Yann, Audic, Frédérique, Behin, Anthony, Friedman, Diane, Magot, Armelle, Noury, Jean-Baptiste, Souvannanorath, Sarah, Wahbi, Karim, Antoine, Jean-Christophe, Bigaut, Kévin, Camdessanché, Jean-Philippe, Cintas, Pascal, Debs, Rabab, Espil-Taris, Caroline, Kremer, Laurent, Kuntzer, Thierry, Laforêt, Pascal, Laugel, Vincent, Mallaret, Martial, Michaud, Maud, Nollet, Sylvain, Svahn, Juliette, Vicart, Savine, Villar-Quiles, Rocio Nur, Desguerre, Isabelle, Adams, David, Segovia-Kueny, Sandrine, Merret, Géraldine, Hammouda, Elhadi, Molon, Annamaria, Attarian, Shahram

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Limb-Girdle Muscular Dystrophy type R9 linked to the FKRP gene: state of the art and therapeutic perspectives von Villar Quiles, Rocío Nur, Richard, Isabelle, Bouchet-Seraphin, Céline, Stojkovic, Tanya

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Infratrochlear neuralgia: A prospective series of seven patients treated with infratrochlear nerve blocks von Villar-Quiles, Rocío-Nur, García-Moreno, Héctor, Mayo, Diego, Gutiérrez-Viedma, Álvaro, Ramos, María-Isabel, Casas-Limón, Javier, Cuadrado, María-Luz

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Diagnostic yield of a practical electrodiagnostic protocol discriminating between different congenital myasthenic syndromes von Stojkovic, Tanya, Masingue, Marion, Turmel, Helène, Hezode-Arzel, Marianne, Béhin, Anthony, Leonard-Louis, Sarah, Bassez, Guillaume, Bauché, Stéphanie, Blondy, Patricia, Richard, Pascale, Sternberg, Damien, Eymard, Bruno, Fournier, Emmanuel, Villar-Quiles, Rocío Nur

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Teaching Neuro Images : Adult-onset leukoencephalopathy with intracranial calcifications and cysts (Labrune syndrome) von Villar-Quiles, Rocío-Nur, Gómez-Ruiz, Natividad, Jorquera-Moya, Manuela, Matías-Guiu, Jorge, Matias-Guiu, Jordi A

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Teaching NeuroImages: Adult-onset leukoencephalopathy with intracranial calcifications and cysts (Labrune syndrome) von Villar-Quiles, Rocío-Nur, Gómez-Ruiz, Natividad, Jorquera-Moya, Manuela, Matías-Guiu, Jorge, Matias-Guiu, Jordi A

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Dystrophie musculaire liée à des mutations du gène JAG2: L’importance du diagnostic différentiel von Nur Villar-Quiles, Rocio, Romero, Norma B, Tanya, Stojkovic

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Caveolinopathy: Clinical, histological, and muscle imaging features and follow‐up in a multicenter retrospective cohort von Berling, Edouard, Verebi, Camille, Venturelli, Nadia, Vassilopoulos, Stéphane, Béhin, Anthony, Tard, Céline, Michaud, Maud, Villar Quiles, Rocio Nur, Vicart, Savine, Masingue, Marion, Carlier, Robert‐yves, Romero, Norma Beatriz, Lacene, Emmanuelle, Leturcq, France, Eymard, Bruno, Laforêt, Pascal, Stojkovic, Tanya

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