Churg–Strauss Syndrome Revealed by Granulomatous Acute Pericarditis: Two Case Reports and a Review of the Literature by 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 by 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 by 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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De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome by 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 by 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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Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32 by 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 by 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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Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients by 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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Next-generation sequencing allows a diagnostic yield of 23.7% in monogenic epilepsies by 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 by 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 by 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 by 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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Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination by 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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Glial cell line-derived neurotrophic factor (GDNF) gene expression in the human brain : a post mortem in situ hybridization study with special reference to Parkinson's disease by HUNOT, S, BERNARD, V, HIRSCH, E. C, FAUCHEUX, B, BOISSIERE, F, LEGUERN, E, BRANA, C, GAUTRIS, P. P, GUERIN, J, BLOCH, B, AGID, Y

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Fine Mapping of de Novo CMT1A and HNPP Rearrangements within CMTIA-REPs Evidences Two Distinct Sex-Dependent Mechanisms and Candidate Sequences Involved in Recombination by Lopes, Judith, Ravisé, Nicole, Vandenberghe, Antoon, Palau, Francisco, Ionasescu, Victor, Mayer, Michelle, Lévy, Nicolas, Wood, Nicholas, Tachi, Nobutada, Bouche, Pierre, Latour, Philippe, Ruberg, Merle, Brice, Alexis, LeGuern, Eric

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PRENATAL DETECTION OF A 17P11.2 DUPLICATION RESULTING FROM A RARE RECOMBINATION EVENT AND NOVEL PCR-BASED STRATEGY FOR MOLECULAR IDENTIFICATION OF CHARCOT-MARIE-TOOTH DISEASE TYPE... by Bernard, R, Labelle, V, Negre, P, Tardieu, S, Azulay, Jp, Malzac, P, Mattei, Jf, Leguern, E, Philip, N, Levy, N.

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PRENATAL DETECTION OF A 17P11.2 DUPLICATION RESULTING FROM A RARE RECOMBINATION EVENT AND NOVEL PCR-BASED STRATEGY FOR MOLECULAR IDENTIFICATION OF CHARCOT-MARIE-TOOTH DISEASE TYPE... by Bernard, R, Labelle, V, Negre, P, Tardieu, S, Azulay, Jp, Malzac, P, Mattei, Jf, Leguern, E, Philip, N, Levy, N.

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Apolipoprotein E genotype does not affect age at onset in patients with chromosome 14 encoded Alzheimer's disease

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Molecular genetic analysis of the 17p11.2 region in patients with hereditary neuropathy with liability to pressure palsies (HNPP) by TIMMERMAN, V, LÖFGREN, A, VAN BROECKHOVEN, C, LE GUERN, E, PING LIANG, DE JONGHE, P, MARTIN, J.-J, VERHALLE, D, ROBBERECHT, W, GOUIDER, R, BRICE, A

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