Churg–Strauss Syndrome Revealed by Granulomatous Acute Pericarditis: Two Case Reports and a Review of the Literature von Agard, C., MD, Rendu, E., Resident, Leguern, V., MD, Ponge, T., MD, PhD, Masseau, A., MD, Barrier, J.H., MD, Trochu, J.N., MD, PhD, Hamidou, M.A., MD, PhD, Guillevin, L., MD

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Pregnancy and antiphospholipid syndrome von Costedoat-Chalumeau, N, Guettrot-Imbert, G, Leguern, V, Leroux, G, Le Thi Huong, D, Wechsler, B, Morel, N, Vauthier-Brouzes, D, Dommergues, M, Cornet, A, Aumaître, O, Pourrat, O, Piette, J-C, Nizard, J

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Grossesse et syndrome des antiphospholipides von Costedoat-Chalumeau, N., Guettrot-Imbert, G., Leguern, V., Leroux, G., Le Thi Huong, D., Wechsler, B., Morel, N., Vauthier-Brouzes, D., Dommergues, M., Cornet, A., Aumaître, O., Pourrat, O., Piette, J.-C., Nizard, J.

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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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De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome von Suls, Arvid, Jaehn, Johanna A., Kecskés, Angela, Weber, Yvonne, Weckhuysen, Sarah, Craiu, Dana C., Siekierska, Aleksandra, Djémié, Tania, Afrikanova, Tatiana, Gormley, Padhraig, von Spiczak, Sarah, Kluger, Gerhard, Iliescu, Catrinel M., Talvik, Tiina, Talvik, Inga, Meral, Cihan, Caglayan, Hande S., Giraldez, Beatriz G., Serratosa, José, Lemke, Johannes R., Hoffman-Zacharska, Dorota, Szczepanik, Elzbieta, Barisic, Nina, Komarek, Vladimir, Hjalgrim, Helle, Møller, Rikke S., Linnankivi, Tarja, Dimova, Petia, Striano, Pasquale, Zara, Federico, Marini, Carla, Guerrini, Renzo, Depienne, Christel, Baulac, Stéphanie, Kuhlenbäumer, Gregor, Crawford, Alexander D., Lehesjoki, Anna-Elina, de Witte, Peter A.M., Palotie, Aarno, Lerche, Holger, Esguerra, Camila V., De Jonghe, Peter, Helbig, Ingo, Hendrickx, Rik, Holmgren, Philip, Stephani, Ulrich, Muhle, Hiltrud, Pendiziwiat, Manuela, Appenzeller, Silke, Selmer, Kaja, Brilstra, Eva, Koeleman, Bobby, Rosenow, Felix, Leguern, Eric, Sterbova, Katalin, Magdalena, Budisteanu, Rodica, Gherghiceanu, Arsene, Oana Tarta, Diana, Barca, Guerrero-Lopez, Rosa, Ortega, Laura, Todorova, Albena P., Kirov, Andrey V., Robbiano, Angela, Arslan, Mutluay, Yiş, Uluç, Ivanović, Vanja

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A humanized IL-2 mutein expands Tregs and prolongs transplant survival in preclinical models von Efe, Orhan, Gassen, Rodrigo B, Morena, Leela, Ganchiku, Yoshikazu, Al Jurdi, Ayman, Lape, Isadora T, Ventura-Aguiar, Pedro, LeGuern, Christian, Madsen, Joren C, Shriver, Zachary, Babcock, Gregory J, Borges, Thiago J, Riella, Leonardo V

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Abrogation of Renal Allograft Tolerance in MGH Miniature Swine: The Role of Intra‐Graft and Peripheral Factors in Long‐Term Tolerance von Scalea, J. R., Okumi, M., Villani, V., Shimizu, A., Nishimura, H., Gillon, B. C., Torabi, R., Cormack, T., Moran, S., LeGuern, C., Sachs, D. H., Yamada, K.

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Abnormal TDP-43 and FUS proteins in muscles of sporadic IBM: similarities in a TARDBP-linked ALS patient von Hernandez Lain, Aurelio, Millecamps, Stéphanie, Dubourg, Odile, Salachas, François, Bruneteau, Gaëlle, Lacomblez, Lucette, LeGuern, Eric, Seilhean, Danielle, Duyckaerts, Charles, Meininger, Vincent, Mallet, Jacques, Pradat, Pierre-François

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Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 von STEFFEN, Michael Steffen, LEU, Costin, LA NEVE, Angela, CRICHIUTTI, Giovanni, DE KOVEL, Carolien G. F, TRENITE, Dorothée Kasteleijn-Nolst, DE HAAN, Gerrit-Jan, LINDHOUT, Dick, GAUS, Verena, SCHMITZ, Bettina, JANZ, Dieter, WEBER, Yvonne G, RUPPERT, Ann-Kathrin, BECKER, Felicitas, LERCHE, Holger, STEINHOFF, Bernhard J, KLEEFUSS-LIE, Ailing A, KUNZ, Wolfram S, SURGES, Rainer, ELGER, Christian E, MUHLE, Hiltrud, VON SPICZAK, Sarah, OSTERTAG, Philipp, ZARA, Federico, HELBIG, Ingo, STEPHANI, Ulrich, MØLLER, Rikke S, HJALGRIM, Helle, DIBBENS, Leanne M, BELLOWS, Susannah, OLIVER, Karen, MULLEN, Saul, SCHEFFER, Ingrid E, BERKOVIC, Samuel F, STRIANO, Pasquale, EVERETT, Kate V, GARDINER, Mark R, MARINI, Carla, GUERRINI, Renzo, LEHESJOKI, Anna-Elina, SIREN, Auli, ROBBIANO, Angela, CAPOVILLA, Giuseppe, TINUPER, Paolo, GAMBARDELLA, Antonio, BIANCHI, Amedeo

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Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study von Stanley, Kate E., Bobbili, Dheeraj R., Dhindsa, Ryan S., May, Patrick, Alldredge, Brian K., Allen, Andrew S., Altmüller, Janine, Amrom, Dina, Andermann, Eva, Auce, Pauls, Avbersek, Andreja, Bautista, Jocelyn F., Becker, Felicitas, Bellows, Susannah T., Berghuis, Bianca, Bluvstein, Judith, Boro, Alex, Burgess, Rosemary, Caglayan, Hande, Cascino, Gregory D., Chung, Seo‐Kyung, Cieuta‐Walti, Cécile, Consalvo, Damian, Cossette, Patrick, Crumrine, Patricia, Delanty, Norman, Depondt, Chantal, Desbiens, Richard, Dlugos, Dennis, Epstein, Michael P., Everett, Kate, Fountain, Nathan B., Francis, Ben, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Girard, Simon, Glauser, Tracy, Glynn, Simon, Gravel, Micheline, Haas, Kevin, Haut, Sheryl R., Heinzen, Erin L., Helbig, Ingo, Hildebrand, Michael S., Jorgensen, Andrea, Joshi, Sucheta, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Kossoff, Eric H., Krause, Roland, Kunz, Wolfram S., Langley, Sarah R., LeGuern, Eric, Lerche, Holger, Leu, Costin, Lortie, Anne, Marson, Anthony G., Mebane, Caroline, Mefford, Heather C., Meloche, Caroline, Motika, Paul V., Muhle, Hiltrud, Nabbout, Rima, Nguyen, Dang K., Nikanorova, Marina, Novotny, Edward J., Ottman, Ruth, O’Brien, Terence J., Paolicchi, Juliann M., Parent, Jack M., Peter, Sarah, Petrou, Steven, Pickrell, William O., Poduri, Annapurna, Radtke, Rodney A., Rees, Mark I., Regan, Brigid M., Sadleir, Lynette G., Sander, Josemir W., Sander, Thomas, Scheffer, Ingrid E., Singh, Rani K., Sirven, Joseph, Sisodiya, Sanjay M., Smith, Michael C., Sonsma, Anja C. M., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Von Allmen, Gretchen K., Wang, Quanli, Weber, Yvonne G., Weckhuysen, Sarah, Widdess‐Walsh, Peter, Winawer, Melodie R., Wolking, Stefan, Zimprich, Fritz

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Late-onset metachromatic leukodystrophy : Genotype strongly influences phenotype von RAUSCHKA, H, COLSCH, B, KRIVIT, W, MOSER, H, MOSER, A, GIESELMANN, V, ZALC, B, COX, T, REUNER, U, TYLKI-SZYMANSKA, A, ABOUL-ENEIN, F, LEGUERN, E, BAUMANN, N, BERNHEIMER, H, BERGER, J, WEVERS, R, SCHMIDBAUER, M, KRAMMER, M, TURPIN, J.-C, LEFEVRE, M, OLIVIER, C, TARDIEU, S

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Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients von Kovel, Carolien G.F., Brilstra, Eva H., Kempen, Marjan J.A., Slot, Ruben, Nijman, Isaac J., Afawi, Zaid, De Jonghe, Peter, Djémié, Tania, Guerrini, Renzo, Hardies, Katia, Helbig, Ingo, Hendrickx, Rik, Kanaan, Moine, Kramer, Uri, Lehesjoki, Anna‐Elina E., Lemke, Johannes R., Marini, Carla, Mei, Davide, Møller, Rikke S., Pendziwiat, Manuela, Stamberger, Hannah, Suls, Arvid, Weckhuysen, Sarah, Koeleman, Bobby P.C., R, Balling, N, Barisic, S, Baulac, HS, Caglayan, DC, Craiu, C, Depienne, P, Gormley, H, Hjalgrim, D, Hoffman‐Zacharska, J, Jähn, KM, Klein, V, Komarek, E, LeGuern, H, Lerche, P, May, H, Muhle, D, Pal, A, Palotie, F, Rosenow, K, Selmer, JM, Serratosa, SM, Sisodiya, U, Stephani, K, Sterbova, P, Striano, T, Talvik, M, van Haelst, N, Verbeek, S, von Spiczak, YG, Weber

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The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V von DUBOURG, O, AZZEDINE, H, BEN YAOU, R, POUGET, J, BAROIS, A, MEININGER, V, BOUTEILLER, D, RUBERG, M, BRICE, A, LEGUERN, E

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Next-generation sequencing allows a diagnostic yield of 23.7% in monogenic epilepsies von Lesca, G, Labalme, A, Mignot, C, Chatron, N, Van de Velde Boermans, L, des Portes, V, Bogoin, J, Ville, D, de Belescize, J, Nougues, M.C, Doummar, D, Afenjar, A, Poulat, A.L, Panagiotakaki, E, Valence, S, Arzimanoglou, A, Heron, D, Leguern, E, Sanlaville, D, Nava, C

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A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease von GUILBOT, Angèle, WILLIAMS, Anna, MEGARBANE, André, CLAUSTRES, Mireille, RAVISE, Nicole, VERNY, Christophe, BRICE, Alexis, SHERMAN, Diane L, BROPHY, Peter J, LEGUERN, Eric, DELAGUE, Valérie, BAREIL, Corinne

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K-complex-induced seizures in autosomal dominant nocturnal frontal lobe epilepsy von El Helou, J, Navarro, V, Depienne, C, Fedirko, E, LeGuern, E, Baulac, M, An-Gourfinkel, I, Adam, C

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Correction to: Imported falciparum malaria in adults: host- and parasite-related factors associated with severity. The French prospective multicenter PALUREA cohort study von Bruneel, Fabrice, Tubach, Florence, Mira, Jean-Paul, Houze, Sandrine, Gibot, Sebastien, Huisse, Marie-Genevieve, Megarbane, Bruno, Choquet, Christophe, Corne, Philippe, Peytel, Eric, Villers, Daniel, Camus, Christophe, Bouchaud, Olivier, Caumes, Eric, Girard, Pierre-Marie, Simon, Fabrice, Kalloumeh, Antoine, Roy, Carine, Durand, Remy, Le Bras, Jacques, Matheron, Sophie, Wolff, Michel

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De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome von Suls, Arvid, Jaehn, Johanna A, Kecskés, Angela, Weber, Yvonne, Weckhuysen, Sarah, Craiu, Dana C, Siekierska, Aleksandra, Djémié, Tania, Afrikanova, Tatiana, Gormley, Padhraig, von Spiczak, Sarah, Kluger, Gerhard, Iliescu, Catrinel M, Talvik, Tiina, Talvik, Inga, Meral, Cihan, Caglayan, Hande S, Giraldez, Beatriz G, Serratosa, José, Lemke, Johannes R, Hoffman-Zacharska, Dorota, Szczepanik, Elzbieta, Barisic, Nina, Komarek, Vladimir, Hjalgrim, Helle, Møller, Rikke S, Linnankivi, Tarja, Dimova, Petia, Striano, Pasquale, Zara, Federico, Marini, Carla, Guerrini, Renzo, Depienne, Christel, Baulac, Stéphanie, Kuhlenbäumer, Gregor, Crawford, Alexander D, Lehesjoki, Anna-Elina, de Witte, Peter A.M, Palotie, Aarno, Lerche, Holger, Esguerra, Camila V, De Jonghe, Peter, Helbig, Ingo, the EuroEPINOMICS RES Consortium

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Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination von LOPES, J, RAVISE, N, LATOUR, P, RUBERG, M, BRICE, A, LEGUERN, E, VANDENBERGHE, A, PALAU, F, IONASESCU, V, MAYER, M, LEVY, N, WOOD, N, TACHI, N, BOUCHE, P

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Longitudinal study assessing the return of chloroquine susceptibility of Plasmodium falciparum in isolates from travellers returning from West and Central Africa, 2000-2011 von Gharbi, M, Flegg, JA, Hubert, V, Kendjo, E, Metcalf, JE, Bertaux, L, Guérin, PJ, Le Bras, J, Members of the French National Reference Centre for Imported Malaria Study, Aboubaca, A, Agnamey, P, Angoulvant, A, Barbut, P, Basset, D, Belkadi, G, Bellanger, AP, Bemba, D, Benoit-Vica, F, Berry, A, Bigel, ML, Bonhomme, J, Botterel, F, Bouchaud, O, Bougnoux, ME, Bourée, P, Bourgeois, N, Branger, C, Bret, L, Buret, B, Casalino, E, Chevrier, S, Conquere de Monbrison, F, Cuisenier, B, Danis, M, Darde, ML, De Gentile, L, Delarbre, JM, Delaunay, P, Delaval, A, Desoubeaux, G, Develoux, M, Dunand, J, Durand, R, Eloy, O, Fauchet, N, Faugere, B, Faye, A, Fenneteau, O, Flori, P, Fontrouge, M, Garabedian, C, Gayandrieu, F, Godineau, N, Houzé, P, Houzé, S, Hurst, JP, Ichou, H, Lachaud, L, Lebuisson, A, Lefevre, M, LeGuern, AS, Le Moal, G, Lusina, D, Machouart, MC, Malvy, D, Matheron, S, Maubon, D, Mechali, D, Megarbane, B, Menard, G, Millon, L, Aiach, MM, Minodier, P, Morelle, C, Nevez, G, Parola, P, Parzy, D, Patey, O, Patoz, P, Penn, P, Perignon, A, Picot, S, Pilo, JE, Poilane, I, Pons, D, Poupart, M, Pradines, B, Raffenot, D, Rapp, C, Receveur, MC, Sarfati, C, Senghor, Y, Simon, F, Siriez, JY, Taudon, N, Thellier, M, Thouvenin, M, Toubas, D

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