The various forms of hereditary motor neuron disorders and their historical descriptions von Mathis, Stéphane, Beauvais, Diane, Duval, Fanny, Solé, Guilhem, Le Masson, Gwendal

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The ataxic neuropathies von Mathis, Stéphane, Duval, Fanny, Soulages, Antoine, Solé, Guilhem, Le Masson, Gwendal

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Clinical and pathological aspects of toxic myopathies von Le Quang, Mégane, Solé, Guilhem, Martin-Négrier, Marie-Laure, Mathis, Stéphane

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Acute peripheral neuropathy following animal envenomation: A case report and systematic review von Mathis, Stéphane, Carla, Louis, Duval, Fanny, Nadal, Louis, Solé, Guilhem, Le Masson, Gwendal

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Usefulness of subcutaneous immunoglobulin therapy in the management of myasthenia gravis: a retrospective cohort study von Barnay, Marlène, Duval, Fanny, Solé, Guilhem, Carla, Louis, Mathis, Stéphane, Le Masson, Gwendal

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Prognostic factor of poor outcome in anti-MAG neuropathy: clinical and electrophysiological analysis of a French Cohort von Tang, Marie-Ange Hoang, Mathis, Stéphane, Duffau, Pierre, Cazenave, Philippe, Solé, Guilhem, Duval, Fanny, Soulages, Antoine, Le Masson, Gwendal

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Olfaction and anosmia: From ancient times to COVID-19 von Mathis, Stéphane, Le Masson, Gwendal, Soulages, Antoine, Duval, Fanny, Carla, Louis, Vallat, Jean-Michel, Solé, Guilhem

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A novel nonsense PIEZO2 mutation in a family with scoliosis and proprioceptive defect von Masingue, Marion, Fauré, Julien, Solé, Guilhem, Stojkovic, Tanya, Léonard-Louis, Sarah

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Phenotype variability and natural history of X-linked myopathy with excessive autophagy von Fernández-Eulate, Gorka, Alfieri, Girolamo, Spinazzi, Marco, Ackermann-Bonan, Isabelle, Duval, Fanny, Solé, Guilhem, Caillon, Florence, Mercier, Sandra, Pereon, Yann, Magot, Armelle, Pegat, Antoine, Salort-Campana, Emmanuelle, Chabrol, Brigitte, Gorokhova, Svetlana, Krahn, Martin, Biancalana, Valerie, Evangelista, Teresinha, Behin, Anthony, Metay, Corinne, Stojkovic, Tanya

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Chronic inflammatory demyelinating polyradiculoneuropathy‐causing myelopathy von Mathis, Stéphane, Duval, Fanny, Solé, Guilhem, Tourdias, Thomas, Le Masson, Gwendal

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LRSAM1 variants and founder effect in French families with ataxic form of Charcot-Marie-Tooth type 2 von Peretti, Alessia, Perie, Maud, Vincent, Didier, Bouhour, Françoise, Dieterich, Klaus, Mallaret, Martial, Duval, Fanny, Goizet, Cyril, Juntas-Morales, Raul, Magy, Laurent, Solé, Guilhem, Nollet, Sylvain, Not, Adeline, Léonard-Louis, Sarah, Francou, Bruno, Leguern, Eric, Lia, Anne-Sophie, Magdelaine, Corinne, Latour, Philippe, Stojkovic, Tanya

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Macroglossia: A potentially severe complication of late‐onset Pompe disease von Dupé, Charlotte, Lefeuvre, Claire, Solé, Guilhem, Behin, Anthony, Pottier, Corinne, Duval, Fanny, Carlier, Robert‐Yves, Prigent, Hélène, Lacau St Guily, Jean, Arrassi, Azzeddine, Taouagh, Nadjib, Hamroun, Dalil, Nicolas, Guillaume, Laforêt, Pascal

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Type 1 FSHD with 6-10 Repeated Units: Factors Underlying Severity in Index Cases and Disease Penetrance in Their Relatives Attention von Salort-Campana, Emmanuelle, Fatehi, Farzad, Beloribi-Djefaflia, Sadia, Roche, Stephane, Nguyen, Karine, Bernard, Rafaelle, Cintas, Pascal, Sole, Guilhem, Bouhour, Francoise, Ollagnon, Elisabeth, Sacconi, Sabrina, Echaniz-Laguna, Andoni, Kuntzer, Thierry, Levy, Nicolas, Magdinier, Frederique, Attarian, Shahram

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Neurologic manifestations of giant cell arteritis von Soulages, Antoine, Sibon, Igor, Vallat, Jean-Michel, Ellie, Emmanuel, Bourdain, Frédéric, Duval, Fanny, Carla, Louis, Martin-Négrier, Marie-Laure, Solé, Guilhem, Laurent, Charles, Monnier, Agnès, Le Masson, Gwendal, Mathis, Stéphane

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Thrombocytopenia resulting from mutations in filamin A can be expressed as an isolated syndrome von Nurden, Paquita, Debili, Najet, Coupry, Isabelle, Bryckaert, Marijke, Youlyouz-Marfak, Ibtissam, Solé, Guilhem, Pons, Anne-Cécile, Berrou, Eliane, Adam, Frédéric, Kauskot, Alexandre, Lamazière, Jean-Marie Daniel, Rameau, Philippe, Fergelot, Patricia, Rooryck, Caroline, Cailley, Dorothée, Arveiler, Benoît, Lacombe, Didier, Vainchenker, William, Nurden, Alan, Goizet, Cyril

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Bulbar muscle impairment in patients with late onset Pompe disease: Insight from the French Pompe registry von Retailleau, Emilie, Lefeuvre, Claire, De Antonio, Marie, Bouhour, Françoise, Tard, Celine, Salort‐Campana, Emmanuelle, Lagrange, Emmeline, Béhin, Anthony, Solé, Guilhem, Noury, Jean‐Baptiste, Sacconi, Sabrina, Magot, Armelle, Pakleza, Aleksandra Nadaj, Orlikowski, David, Beltran, Stéphane, Spinazzi, Marco, Cintas, Pascal, Fournier, Maxime, Bouibede, Fatma, Prigent, Hélène, Nicolas, Guillaume, Taouagh, Nadjib, El Guizani, Taissir, Attarian, Shahram, Arrassi, Azzeddine, Hamroun, Dalil, Laforêt, Pascal

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Characterization of novel CACNA1A splice variants by RNA‐sequencing in patients with episodic or congenital ataxia von Riant, Florence, Burglen, Lydie, Corpechot, Michaelle, Robert, Julien, Durr, Alexandra, Solé, Guilhem, Petit, Florence, Freihuber, Cécile, De Marco, Olivier, Sarret, Catherine, Castelnovo, Giovanni, Devillard, Françoise, Afenjar, Alexandra, Héron, Bénédicte, Lasserve, Elisabeth Tournier

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Peripheral neuropathy and livedoid vasculopathy von Soulages, Antoine, Maisonobe, Thierry, Auzou, Pascal, Petit, Antoine, Allenbach, Yves, Barète, Stéphane, Skopinski, Sophie, Ribeiro, Emmanuel, Jullié, Marie-Laure, Lamant, Laurence, Brevet, Françoise, Soulages, Xavier, Vallat, Jean-Michel, Martin-Négrier, Marie-Laure, Solé, Guilhem, Duval, Fanny, Carla, Louis, Le Masson, Gwendal, Mathis, Stéphane

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History and current difficulties in classifying inherited myopathies and muscular dystrophies von Mathis, Stéphane, Tazir, Meriem, Magy, Laurent, Duval, Fanny, Le Masson, Gwendal, Duchesne, Mathilde, Couratier, Philippe, Ghorab, Karima, Solé, Guilhem, Lacoste, Idoia, Goizet, Cyril, Vallat, Jean-Michel

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Home versus hospital immunoglobulin treatment for autoimmune neuropathies: A cost minimization analysis von Le Masson, Gwendal, Solé, Guilhem, Desnuelle, Claude, Delmont, Emilien, Gauthier‐Darnis, Marc, Puget, Sophie, Durand‐Zaleski, Isabelle

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