A ferroptosis–based panel of prognostic biomarkers for Amyotrophic Lateral Sclerosis von Devos, David, Moreau, Caroline, Kyheng, Maeva, Garçon, Guillaume, Rolland, Anne Sophie, Blasco, Hélène, Gelé, Patrick, Timothée Lenglet, T., Veyrat-Durebex, C., Corcia, Philippe, Dutheil, Mary, Bede, Peter, Jeromin, Andreas, Oeckl, Patrick, Otto, Markus, Meininger, Vincent, Danel-Brunaud, Véronique, Devedjian, Jean-christophe, Duce, James A., Pradat, Pierre François

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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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Screening of OPTN in French familial amyotrophic lateral sclerosis von Millecamps, Stéphanie, Boillée, Séverine, Chabrol, Elodie, Camu, William, Cazeneuve, Cécile, Salachas, François, Pradat, Pierre-François, Danel-Brunaud, Véronique, Vandenberghe, Nadia, Corcia, Philippe, Le Forestier, Nadine, Lacomblez, Lucette, Bruneteau, Gaëlle, Seilhean, Danielle, Brice, Alexis, Feingold, Josué, Meininger, Vincent, LeGuern, Eric

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Could Conservative Iron Chelation Lead to Neuroprotection in Amyotrophic Lateral Sclerosis? von Moreau, Caroline, Danel, Véronique, Devedjian, Jean Christophe, Grolez, Guillaume, Timmerman, Kelly, Laloux, Charlotte, Petrault, Maud, Gouel, Flore, Jonneaux, Aurélie, Dutheil, Mary, Lachaud, Cédrick, Lopes, Renaud, Kuchcinski, Grégory, Auger, Florent, Kyheng, Maeva, Duhamel, Alain, Pérez, Thierry, Pradat, Pierre François, Blasco, Hélène, Veyrat-Durebex, Charlotte, Corcia, Philippe, Oeckl, Patrick, Otto, Markus, Dupuis, Luc, Garçon, Guillaume, Defebvre, Luc, Cabantchik, Z Ioav, Duce, James, Bordet, Régis, Devos, David

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Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes von Millecamps, Stéphanie, Boillée, Séverine, Le Ber, Isabelle, Seilhean, Danielle, Teyssou, Elisa, Giraudeau, Marine, Moigneu, Carine, Vandenberghe, Nadia, Danel-Brunaud, Véronique, Corcia, Philippe, Pradat, Pierre-François, Le Forestier, Nadine, Lacomblez, Lucette, Bruneteau, Gaelle, Camu, William, Brice, Alexis, Cazeneuve, Cécile, LeGuern, Eric, Meininger, Vincent, Salachas, François

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Questioning on the role of D amino acid oxidase in familial amyotrophic lateral sclerosis von Millecamps, Stéphanie, Da Barroca, Sandra, Cazeneuve, Cécile, Salachas, François, Pradat, Pierre-François, Danel-Brunaud, Véronique, Vandenberghe, Nadia, Lacomblez, Lucette, Le Forestier, Nadine, Bruneteau, Gaëlle, Camu, William, Brice, Alexis, Meininger, Vincent, LeGuern, Eric

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Que proposer aux apparentés de patients SLA familiale : aspects pratiques et éthiques von Danel, Véronique

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Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders von Lattante, Serena, Millecamps, Stéphanie, Stevanin, Giovanni, Rivaud-Péchoux, Sophie, Moigneu, Carine, Camuzat, Agnès, Da Barroca, Sandra, Mundwiller, Emeline, Couarch, Philippe, Salachas, François, Hannequin, Didier, Meininger, Vincent, Pasquier, Florence, Seilhean, Danielle, Couratier, Philippe, Danel-Brunaud, Véronique, Bonnet, Anne-Marie, Tranchant, Christine, LeGuern, Eric, Brice, Alexis, Le Ber, Isabelle, Kabashi, Edor

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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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Assessing the upper motor neuron in amyotrophic lateral sclerosis using the triple stimulation technique: A multicenter prospective study von Grapperon, Aude-Marie, Verschueren, Annie, Jouve, Elisabeth, Morizot-Koutlidis, Régine, Lenglet, Timothée, Pradat, Pierre-François, Salachas, François, Bernard, Emilien, Delstanche, Stéphanie, Maertens de Noordhout, Alain, Guy, Nathalie, Danel, Véronique, Delval, Arnaud, Delmont, Emilien, Rolland, Anne-Sophie, PULSE Study Group, Jomir, Laurent, Devos, David, Wang, François, Attarian, Shahram

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Author Correction: A ferroptosis–based panel of prognostic biomarkers for Amyotrophic Lateral Sclerosis von Devos, David, Moreau, Caroline, Kyheng, Maeva, Garçon, Guillaume, Rolland, Anne Sophie, Blasco, Hélène, Gelé, Patrick, Lenglet, T. Timothée, Veyrat-Durebex, C., Corcia, Philippe, Dutheil, Mary, Bede, Peter, Jeromin, Andreas, Oeckl, Patrick, Otto, Markus, Meininger, Vincent, Danel-Brunaud, Véronique, Devedjian, Jean-Christophe, Duce, James A., Pradat, Pierre François

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Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis von Millecamps, Stéphanie, Corcia, Philippe, Cazeneuve, Cécile, Boillée, Séverine, Seilhean, Danielle, Danel-Brunaud, Véronique, Vandenberghe, Nadia, Pradat, Pierre-François, Le Forestier, Nadine, Lacomblez, Lucette, Bruneteau, Gaëlle, Camu, William, Brice, Alexis, Meininger, Vincent, LeGuern, Eric, Salachas, François

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Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis von Naumann, Marcel, Peikert, Kevin, Günther, Rene, Kooi, Anneke J., Aronica, Eleonora, Hübers, Annemarie, Danel, Veronique, Corcia, Philippe, Pan‐Montojo, Francisco, Cirak, Sebahattin, Haliloglu, Göknur, Ludolph, Albert C., Goswami, Anand, Andersen, Peter M., Prudlo, Johannes, Wegner, Florian, Van Damme, Philip, Weishaupt, Jochen H., Hermann, Andreas

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Spastic paraplegia due to recessive or dominant mutations in ERLIN2 can convert to ALS von Amador, Maria-Del-Mar, Muratet, François, Teyssou, Elisa, Banneau, Guillaume, Danel-Brunaud, Véronique, Allart, Etienne, Antoine, Jean-Christophe, Camdessanché, Jean-Philippe, Anheim, Mathieu, Rudolf, Gabrielle, Tranchant, Christine, Fleury, Marie-Céline, Bernard, Emilien, Stevanin, Giovanni, Millecamps, Stéphanie

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Supercapacitors for the energy management of electric vehicles von Faggioli, Eugenio, Rena, Piergeorgio, Danel, Veronique, Andrieu, X, Mallant, Ronald, Kahlen, Hans

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SLA et téléconsultation : expérience des Hauts-de-France von Danel, Véronique, Sophie, Peres, Rihab, Caillier, Cathy, Delattre, Rubenstrunk, Anne

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Could Conservative Iron Chelation Lead to Neuroprotection in Amyotrophic Lateral Sclerosis?© Caroline Moreau et al . 2018; Published by Mary Ann Liebert, Inc. This Open Access arti... von Moreau, Caroline, Danel, Véronique, Devedjian, Jean Christophe, Grolez, Guillaume, Timmerman, Kelly, Laloux, Charlotte, Petrault, Maud, Gouel, Flore, Jonneaux, Aurélie, Dutheil, Mary, Lachaud, Cédrick, Lopes, Renaud, Kuchcinski, Grégory, Auger, Florent, Kyheng, Maeva, Duhamel, Alain, Pérez, Thierry, Pradat, Pierre François, Blasco, Hélène, Veyrat-Durebex, Charlotte, Corcia, Philippe, Oeckl, Patrick, Otto, Markus, Dupuis, Luc, Garçon, Guillaume, Defebvre, Luc, Cabantchik, Z. Ioav, Duce, James, Bordet, Régis, Devos, David

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SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations von Millecamps, Stéphanie, Salachas, François, Cazeneuve, Cécile, Gordon, Paul, Bricka, Bernard, Camuzat, Agnès, Guillot-Noël, Léna, Russaouen, Odile, Bruneteau, Gaëlle, Pradat, Pierre-François, Le Forestier, Nadine, Vandenberghe, Nadia, Danel-Brunaud, Véronique, Guy, Nathalie, Thauvin-Robinet, Christel, Lacomblez, Lucette, Couratier, Philippe, Hannequin, Didier, Seilhean, Danielle, Le Ber, Isabelle, Corcia, Philippe, Camu, William, Brice, Alexis, Rouleau, Guy, LeGuern, Eric, Meininger, Vincent

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A phase II−III trial of olesoxime in subjects with amyotrophic lateral sclerosis von Lenglet, T., Lacomblez, L., Abitbol, J. L., Ludolph, A., Mora, J. S., Robberecht, W., Shaw, P. J., Pruss, R. M., Cuvier, V., Meininger, V.

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Phenotype and genotype analysis in amyotrophic lateral sclerosis with TARDBP gene mutations von CORCIA, P, VALDMANIS, P, DANEL-BRUNAUD, V, VANDENBERGHE, N, PRADAT, P. F, COURATIER, P, SALACHAS, F, LUMBROSO, S, ROULEAU, G. A, MEININGER, V, CAMU, W, MILLECAMPS, S, LIONNET, C, BLASCO, H, MOUZAT, K, DAOUD, H, BELZIL, V, MORALES, R, PAGEOT, N

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