High risk of cancer in autoimmune necrotizing myopathies: usefulness of myositis specific antibody von Allenbach, Yves, Keraen, Jeremy, Bouvier, Anne-Marie, Jooste, Valérie, Champtiaux, Nicolas, Hervier, Baptiste, Schoindre, Yoland, Rigolet, Aude, Gilardin, Laurent, Musset, Lucile, Charuel, Jean-Luc, Boyer, Olivier, Jouen, Fabienne, Drouot, Laurent, Martinet, Jeremie, Stojkovic, Tanya, Eymard, Bruno, Laforêt, Pascal, Behin, Antony, Salort-Campana, Emmanuelle, Fain, Olivier, Meyer, Alain, Schleinitz, Nicolas, Mariampillai, Kuberaka, Grados, Aurelie, Benveniste, Olivier

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Resistant myasthenia gravis and rituximab: a monocentric retrospective study on 28 patients von Afanasiev, Vadim, Demeret, Sophie, Bolgert, Francis, Eymard, Bruno, Laforêt, Pascal, Benveniste, Olivier

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Thymic Germinal Centers and Corticosteroids in Myasthenia Gravis: an Immunopathological Study in 1035 Cases and a Critical Review von Truffault, Frédérique, de Montpreville, Vincent, Eymard, Bruno, Sharshar, Tarek, Le Panse, Rozen, Berrih-Aknin, Sonia

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Immune checkpoint inhibitors for progressive multifocal leukoencephalopathy: a new gold standard? von Roos-Weil, Damien, Weiss, Nicolas, Guihot, Amélie, Uzunov, Madalina, Bellanger, Agnès, Eymard, Bruno, Saadoun, David, Houillier, Caroline, Idbaih, Ahmed, Demeret, Sophie, Deback, Claire, Leblond, Véronique, Galanaud, Damien, Shor, Natalia, Pourcher, Valérie

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Autologous Myoblast Transplantation for Oculopharyngeal Muscular Dystrophy: a Phase I/Iia Clinical Study von Périé, Sophie, Trollet, Capucine, Mouly, Vincent, Vanneaux, Valérie, Mamchaoui, Kamel, Bouazza, Belaïd, Marolleau, Jean Pierre, Laforêt, Pascal, Chapon, Françoise, Eymard, Bruno, Butler-Browne, Gillian, Larghero, Jérome, St Guily, Jean Lacau

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Constitutive Activation of the Calcium Sensor STIM1 Causes Tubular-Aggregate Myopathy von Böhm, Johann, Chevessier, Frédéric, De Paula, André Maues, Koch, Catherine, Attarian, Shahram, Feger, Claire, Hantaï, Daniel, Laforêt, Pascal, Ghorab, Karima, Vallat, Jean-Michel, Fardeau, Michel, Figarella-Branger, Dominique, Pouget, Jean, Romero, Norma B., Koch, Marc, Ebel, Claudine, Levy, Nicolas, Krahn, Martin, Eymard, Bruno, Bartoli, Marc, Laporte, Jocelyn

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Diaphragm sniff ultrasound: Normal values, relationship with sniff nasal pressure and accuracy for predicting respiratory involvement in patients with neuromuscular disorders von Fayssoil, Abdallah, Nguyen, Lee S, Ogna, Adam, Stojkovic, Tanya, Meng, Paris, Mompoint, Dominique, Carlier, Robert, Prigent, Helene, Clair, Bernard, Behin, Anthony, Laforet, Pascal, Bassez, Guillaume, Crenn, Pascal, Orlikowski, David, Annane, Djillali, Eymard, Bruno, Lofaso, Frederic

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Necrosis in anti-SRP + and anti-HMGCR + myopathies von Allenbach, Yves, Arouche-Delaperche, Louiza, Preusse, Corinna, Radbruch, Helena, Butler-Browne, Gillian, Champtiaux, Nicolas, Mariampillai, Kuberaka, Rigolet, Aude, Hufnagl, Peter, Zerbe, Norman, Amelin, Damien, Maisonobe, Thierry, Louis-Leonard, Sarah, Duyckaerts, Charles, Eymard, Bruno, Goebel, Hans-Hilmar, Bergua, Cecile, Drouot, Laurent, Boyer, Olivier, Benveniste, Olivier, Stenzel, Werner

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Molecular Analysis of a Congenital Myasthenic Syndrome Due to a Pathogenic Variant Affecting the C-Terminus of ColQ von Barbeau, Susie, Semprez, Fannie, Dobbertin, Alexandre, Merriadec, Laurine, Roussange, Florine, Eymard, Bruno, Sternberg, Damien, Fournier, Emmanuel, Karasoy, Hanice, Martinat, Cécile, Legay, Claire

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New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani–Lenz syndrome von Masingue, Marion, Cattaneo, Olivia, Wolff, Nicolas, Buon, Céline, Sternberg, Damien, Euchparmakian, Morgane, Boex, Myriam, Behin, Anthony, Mamchaouhi, Kamel, Maisonobe, Thierry, Nougues, Marie-Christine, Isapof, Arnaud, Fontaine, Bertrand, Messéant, Julien, Eymard, Bruno, Strochlic, Laure, Bauché, Stéphanie

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Comparison of juvenile and adult myasthenia gravis in a French cohort with focus on thymic histology von Truffault, Frédérique, Auger, Ludivine, Dragin, Nadine, Vilquin, Jean-Thomas, Fadel, Elie, Thomas de Montpreville, Vincent, Mansuet-Lupo, Audrey, Regnard, Jean-François, Alifano, Marco, Sharshar, Tarek, Behin, Anthony, Eymard, Bruno, Bolgert, Francis, Demeret, Sophie, Berrih-Aknin, Sonia, Le Panse, Rozen

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Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E von Semplicini, Claudio, Vissing, John, Dahlqvist, Julia R, Stojkovic, Tanya, Bello, Luca, Witting, Nanna, Duno, Morten, Leturcq, France, Bertolin, Cinzia, DʼAmbrosio, Paola, Eymard, Bruno, Angelini, Corrado, Politano, Luisa, Laforêt, Pascal, Pegoraro, Elena

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Mutations of the FHL1 Gene Cause Emery-Dreifuss Muscular Dystrophy von Gueneau, Lucie, Bertrand, Anne T., Jais, Jean-Philippe, Salih, Mustafa A., Stojkovic, Tanya, Wehnert, Manfred, Hoeltzenbein, Maria, Spuler, Simone, Saitoh, Shinji, Verschueren, Annie, Tranchant, Christine, Beuvin, Maud, Lacene, Emmanuelle, Romero, Norma B., Heath, Simon, Zelenika, Diana, Voit, Thomas, Eymard, Bruno, Ben Yaou, Rabah, Bonne, Gisèle

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Th1 response and systemic treg deficiency in inclusion body myositis von Allenbach, Yves, Chaara, Wahiba, Rosenzwajg, Michelle, Six, Adrien, Prevel, Nicolas, Mingozzi, Federico, Wanschitz, Julia, Musset, Lucile, Charuel, Jean-Luc, Eymard, Bruno, Salomon, Benoit, Duyckaerts, Charles, Maisonobe, Thierry, Dubourg, Odile, Herson, Serge, Klatzmann, David, Benveniste, Olivier

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A nomenclature and classification for the congenital myasthenic syndromes: preparing for FAIR data in the genomic era von Thompson, Rachel, Abicht, Angela, Beeson, David, Engel, Andrew G, Eymard, Bruno, Maxime, Emmanuel, Lochmüller, Hanns

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Moderate phenotype of a congenital myasthenic syndrome type 19 caused by mutation of the COL13A1 gene: a case report von Kediha, Mohamed Islam, Tazir, Meriem, Sternberg, Damien, Eymard, Bruno, Alipacha, Lamia

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A novel FLNC frameshift and an OBSCN variant in a family with distal muscular dystrophy von Rossi, Daniela, Palmio, Johanna, Evilä, Anni, Galli, Lucia, Barone, Virginia, Caldwell, Tracy A, Policke, Rachel A, Aldkheil, Esraa, Berndsen, Christopher E, Wright, Nathan T, Malfatti, Edoardo, Brochier, Guy, Pierantozzi, Enrico, Jordanova, Albena, Guergueltcheva, Velina, Romero, Norma Beatriz, Hackman, Peter, Eymard, Bruno, Udd, Bjarne, Sorrentino, Vincenzo

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Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations von BÖHM, Johann, BIANCALANA, Valérie, LAFORET, Pascal, MAISONOBE, Thierry, OLIVE, Montse, GONZALEZ-MERA, Laura, FARDEAU, Michel, CARRIERE, Nathalie, CLAVELOU, Pierre, EYMARD, Bruno, BITOUN, Marc, RENDU, John, MALFATTI, Edoardo, FAURE, Julien, WEIS, Joachim, MANDEL, Jean-Louis, ROMERO, Norma B, LAPORTE, Jocelyn, DONDAINE, Nicolas, KOCH, Catherine, VASLI, Nasim, KRESS, Wolfram, STRITTMATTER, Matthias, TARATUTO, Ana Lia, GONORAZKY, Hernan

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Atypical phenotypes in titinopathies explained by second titin mutations von Evilä, Anni, Vihola, Anna, Sarparanta, Jaakko, Raheem, Olayinka, Palmio, Johanna, Sandell, Satu, Eymard, Bruno, Illa, Isabel, Rojas-Garcia, Ricard, Hankiewicz, Karolina, Negrão, Luis, Löppönen, Tuija, Nokelainen, Pekka, Kärppä, Mikko, Penttilä, Sini, Screen, Mark, Suominen, Tiina, Richard, Isabelle, Hackman, Peter, Udd, Bjarne

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Perindopril preventive treatment on mortality in Duchenne muscular dystrophy: 10 years' follow-up von Duboc, Denis, MD, PhD, Meune, Christophe, MD, PhD, Pierre, Bertrand, MD, Wahbi, Karim, MD, Eymard, Bruno, MD, PhD, Toutain, Annick, MD, Berard, Carole, MD, Vaksmann, Guy, MD, Weber, Simon, MD, PhD, Bécane, Henri-Marc, MD

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