Caffeine consumption outcomes on amyotrophic lateral sclerosis disease progression and cognition von Huin, Vincent, Blum, David, Delforge, Violette, Cailliau, Emeline, Djeziri, Sofia, Dujardin, Kathy, Genet, Alexandre, Viard, Romain, Attarian, Shahram, Bruneteau, Gaelle, Cassereau, Julien, Genestet, Steeve, Kaminsky, Anne-Laure, Soriani, Marie-Hélène, Lefilliatre, Mathilde, Couratier, Philippe, Pittion-Vouyovitch, Sophie, Esselin, Florence, De La Cruz, Elisa, Guy, Nathalie, Kolev, Ivan, Corcia, Philippe, Cintas, Pascal, Desnuelle, Claude, Buée, Luc, Danel-Brunaud, Véronique, Devos, David, Rolland, Anne-Sophie

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The Hexokinase 1 5'-UTR Mutation in Charcot-Marie-Tooth 4G Disease Alters Hexokinase 1 Binding to Voltage-Dependent Anion Channel-1 and Leads to Dysfunctional Mitochondrial Calcium... von Ceprian, Maria, Juntas-Morales, Raul, Campbell, Graham, Walther-Louvier, Ulrike, Rivier, François, Camu, William, Esselin, Florence, Echaniz-Laguna, Andoni, Stojkovic, Tanya, Bouhour, Françoise, Latour, Philippe, Tricaud, Nicolas

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Clinical Phenotype and Inheritance in Patients With C9ORF72 Hexanucleotide Repeat Expansion: Results From a Large French Cohort von Esselin, Florence, Mouzat, Kevin, Polge, Anne, Juntas-Morales, Raul, Pageot, Nicolas, De la Cruz, Elisa, Bernard, Emilien, Lagrange, Emmeline, Danel, Véronique, Alphandery, Sébastien, Labar, Laura, Nogué, Erika, Picot, Marie-Christine, Lumbroso, Serge, Camu, William

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Low 25OH Vitamin D Blood Levels Are Independently Associated With Higher Amyotrophic Lateral Sclerosis Severity Scores: Results From a Prospective Study von Juntas-Morales, Raul, Pageot, Nicolas, Marin, Gregory, Dupuy, Anne-Marie, Alphandery, Sébastien, Labar, Laura, Esselin, Florence, Picot, Marie Christine, Camu, William

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Serum neurofilament light chain cut‐off definition for clinical diagnosis and prognosis of amyotrophic lateral sclerosis von Brousse, Mehdi, Delaby, Constance, De La Cruz, Elisa, Kuhle, Jens, Benkert, Pascal, Mondesert, Etienne, Ginestet, Nelly, Hirtz, Christophe, Camu, William, Lehmann, Sylvain, Esselin, Florence

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The IHexokinase 1/I 5′-UTR Mutation in Charcot–Marie–Tooth 4G Disease Alters Hexokinase 1 Binding to Voltage-Dependent Anion Channel-1 and Leads to Dysfunctional Mitochondrial Calc... von Ceprian, Maria, Juntas-Morales, Raul, Campbell, Graham, Walther-Louvier, Ulrike, Rivier, François, Camu, William, Esselin, Florence, Echaniz-Laguna, Andoni, Stojkovic, Tanya, Bouhour, Françoise, Latour, Philippe, Tricaud, Nicolas

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Congenital myasthenic syndromes in adults: clinical features, diagnosis and long-term prognosis von Theuriet, Julian, Masingue, Marion, Behin, Anthony, Ferreiro, Ana, Bassez, Guillaume, Jaubert, Pauline, Tarabay, Oriana, Fer, Frédéric, Pegat, Antoine, Bouhour, Françoise, Svahn, Juliette, Petiot, Philippe, Jomir, Laurentiu, Chauplannaz, Guy, Cornut-Chauvinc, Catherine, Manel, Véronique, Salort-Campana, Emmanuelle, Attarian, Shahram, Fortanier, Etienne, Verschueren, Annie, Kouton, Ludivine, Camdessanché, Jean-Philippe, Tard, Céline, Magot, Armelle, Péréon, Yann, Noury, Jean-Baptiste, Minot-Myhie, Marie-Christine, Perie, Maud, Taithe, Frederic, Farhat, Yacine, Millet, Anne-Laure, Cintas, Pascal, Solé, Guilhem, Spinazzi, Marco, Esselin, Florence, Renard, Dimitri, Sacconi, Sabrina, Ezaru, Andra, Malfatti, Edoardo, Mallaret, Martial, Magy, Laurent, Diab, Eva, Merle, Philippe, Michaud, Maud, Fournier, Maxime, Pakleza, Aleksandra Nadaj, Chanson, Jean-Baptiste, Lefeuvre, Claire, Laforet, Pascal, Richard, Pascale, Sternberg, Damien, Villar-Quiles, Rocio-Nur, Stojkovic, Tanya, Eymard, Bruno

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Characteristics of Patients With Late Onset Pompe Disease in France: Insights From the French Pompe Registry in 2022 von LEFEUVRE, CLAIRE, ANTONIO, MARIE DE, BOUHOUR, FRANCOISE, TARD, CELINE, SALORT-CAMPANA, EMMANUELLE, LAGRANGE, EMMELINE, BEHIN, ANTHONY, SOLE, GUILHEM, NOURY, JEAN-BAPTISTE, Sacconi, Sabrina, MAGOT, ARMELLE, NADAJ-PAKLEZA, ALEKSANDRA, LACOUR, ARNAUD, BELTRAN, STEPHANE, SPINAZZI, MARCO, CINTAS, PASCAL, RENARD, DIMITRI, Michaud, Maud, BEDAT-MILLET, ANNE-LAURE, PRIGENT, HELENE, TAOUAGH, NADJIB, ARRASSI, AZZEDDINE, HAMROUN, DALIL, Attarian, Shahram, Laforêt, Pascal

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Repeated neurofilament light chain measurements did not capture Riluzole therapeutic effect in amyotrophic lateral sclerosis patients von Esselin, Florence, De la Cruz, Elisa, Hirtz, Christophe, Tiers, Laurent, Alphandery, Sébastien, Baudesson, Léandra, Taieb, Guillaume, Camu, William, Lehmann, Sylvain

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Spatio-temporal clustering of amyotrophic lateral sclerosis in France: A population-based study von Boumédiene, Farid, Marin, Benoît, Luna, Jaime, Bonneterre, Vincent, Camu, William, Lagrange, Emmeline, Besson, Gérard, Esselin, Florence, De La Cruz, Elisa, Lautrette, Géraldine, Preux, Pierre Marie, Couratier, Philippe

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The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration von Opie-Martin, Sarah, Iacoangeli, Alfredo, Topp, Simon D., Abel, Olubunmi, Mayl, Keith, Mehta, Puja R., Shatunov, Aleksey, Fogh, Isabella, Bowles, Harry, Limbachiya, Naomi, Spargo, Thomas P., Al-Khleifat, Ahmad, Williams, Kelly L., Jockel-Balsarotti, Jennifer, Bali, Taha, Self, Wade, Henden, Lyndal, Nicholson, Garth A., Ticozzi, Nicola, McKenna-Yasek, Diane, Tang, Lu, Shaw, Pamela J., Chio, Adriano, Ludolph, Albert, Weishaupt, Jochen H., Landers, John E., Glass, Jonathan D., Mora, Jesus S., Robberecht, Wim, Damme, Philip Van, McLaughlin, Russell, Hardiman, Orla, van den Berg, Leonard, Veldink, Jan H., Corcia, Phillippe, Stevic, Zorica, Siddique, Nailah, Silani, Vincenzo, Blair, Ian P., Fan, Dong-sheng, Esselin, Florence, de la Cruz, Elisa, Camu, William, Basak, Nazli A., Siddique, Teepu, Miller, Timothy, Brown, Robert H., Al-Chalabi, Ammar, Shaw, Christopher E.

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Ultrasensitive digital immunoassays for SOD1 conformation in amyotrophic lateral sclerosis von Morichon, Lisa, Hirtz, Christophe, Tiers, Laurent, Mezghrani, Alexandre, Raoul, Cédric, Esselin, Florence, La Cruz, Elisa De, Julien, Jean-Pierre, Camu, William, Lehmann, Sylvain

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HINT1 neuropathy: Expanding the genotype and phenotype spectrum von Morel, Victor, Campana‐Salort, Emmanuelle, Boyer, Amandine, Esselin, Florence, Walther‐Louvier, Ulrike, Querin, Giorgia, Latour, Philippe, Lia, Anne‐Sophie, Magdelaine, Corinne, Beze‐Beyrie, Pierre, Behin, Anthony, Delague, Valérie, Levy, Nicolas, Stojkovic, Tanya, Attarian, Shahram, Bonello‐Palot, Nathalie

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Immune‐mediated diseases involving central and peripheral nervous systems von Leboyan, Aurelie, Esselin, Florence, Bascou, Anne‐Laure, Duflos, Claire, Ion, Ioana, Charif, Mahmoud, Castelnovo, Giovanni, Carra‐Dalliere, Clarisse, Ayrignac, Xavier, Kerschen, Philippe, Chbicheb, Mohamed, Nguyen, Ludovic, Maria, Alexandre T. J., Guilpain, Philippe, Carriere, Mathilde, Champfleur, Nicolas Menjot, Vincent, Thierry, Jentzer, Alexandre, Labauge, Pierre, Devaux, Jérôme J., Taieb, Guillaume

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Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration von Opie-Martin, Sarah, Iacoangeli, Alfredo, Topp, Simon D., Abel, Olubunmi, Mayl, Keith, Mehta, Puja R., Shatunov, Aleksey, Fogh, Isabella, Bowles, Harry, Limbachiya, Naomi, Spargo, Thomas P., Al-Khleifat, Ahmad, Williams, Kelly L., Jockel-Balsarotti, Jennifer, Bali, Taha, Self, Wade, Henden, Lyndal, Nicholson, Garth A., Ticozzi, Nicola, McKenna-Yasek, Diane, Tang, Lu, Shaw, Pamela J., Chio, Adriano, Ludolph, Albert, Weishaupt, Jochen H., Landers, John E., Glass, Jonathan D., Mora, Jesus S., Robberecht, Wim, Damme, Philip Van, McLaughlin, Russell, Hardiman, Orla, van den Berg, Leonard, Veldink, Jan H., Corcia, Phillippe, Stevic, Zorica, Siddique, Nailah, Silani, Vincenzo, Blair, Ian P., Fan, Dong-sheng, Esselin, Florence, de la Cruz, Elisa, Camu, William, Basak, Nazli A., Siddique, Teepu, Miller, Timothy, Brown, Robert H., Al-Chalabi, Ammar, Shaw, Christopher E.

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The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration von Opie-Martin, Sarah, Iacoangeli, Alfredo, Topp, Simon D, Abel, Olubunmi, Mayl, Keith, Mehta, Puja R, Shatunov, Aleksey, Fogh, Isabella, Bowles, Harry, Limbachiya, Naomi, Spargo, Thomas P, Al-Khleifat, Ahmad, Williams, Kelly L, Jockel-Balsarotti, Jennifer, Bali, Taha, Self, Wade, Henden, Lyndal, Nicholson, Garth A, Ticozzi, Nicola, McKenna-Yasek, Diane, Tang, Lu, Shaw, Pamela J, Chio, Adriano, Ludolph, Albert, Weishaupt, Jochen H, Landers, John E, Glass, Jonathan D, Mora, Jesus S, Robberecht, Wim, Van Damme, Philip, McLaughlin, Russell, Hardiman, Orla, van den Berg, Leonard, Veldink, Jan H, Corcia, Phillippe, Stevic, Zorica, Siddique, Nailah, Silani, Vincenzo, Blair, Ian P, Fan, Dong-sheng, Esselin, Florence, de la Cruz, Elisa, Camu, William, Basak, Nazli A, Siddique, Teepu, Miller, Timothy, Brown, Robert H, Al-Chalabi, Ammar, Shaw, Christopher E

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Convergence of patient- and physician-reported outcomes in the French National Registry of Facioscapulohumeral Dystrophy von Sanson, Benoît, Stalens, Caroline, Guien, Céline, Villa, Luisa, Eng, Catherine, Rabarimeriarijaona, Sitraka, Bernard, Rafaëlle, Cintas, Pascal, Solé, Guilhem, Tiffreau, Vincent, Echaniz-Laguna, Andoni, Magot, Armelle, Juntas Morales, Raul, Boyer, François Constant, Nadaj-Pakleza, Aleksandra, Jacquin-Piques, Agnès, Béroud, Christophe, Sacconi, Sabrina

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Nouveaux essais en neuroprotection dans la sclérose latérale amyotrophique von Camu, William, De La Cruz, Elisa, Esselin, Florence

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Thérapie génique dans la SLA von Camu, William, Esselin, Florence, de La Cruz, Elisa

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Analyse de la morbidité de la SLA : que nous apprend le PMSI national ? von Florence, Esselin, Gaudry, Jean-Luc, Sabbagh, Constance, Duchesne, Aude-Marie, Camu, William

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