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Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Publié le 19 mars 2015
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Auteurs
Sawcer S, Hellenthal G, Pirinen M, Spencer C C A, Patsopoulos N A, Moutsianas L, Dilthey A, Su Z, Freeman C, Hunt S E, Edkins S, Gray E, Booth D R, Potter S C, Goris A, Band G, Oturai A B, Strange A, Saarela J, Bellenguez C, Fontaine B, Gillman M, Hemmer B, Gwilliam R, Zipp F, Jayakumar A, Martin R, Leslie S, Hawkins S, Giannoulatou E, D'Alfonso S, Blackburn H, Boneschi F M, Liddle J, Harbo H F, Perez M L, Spurkland A, Waller M J, Mycko M P, Ricketts M, Comabella M, Hammond N, Kockum I, McCann O T, Ban M, Whittaker P, Kemppinen A, Weston P, Hawkins C, Widaa S, Zajicek J, Dronov S, Robertson N, Bumpstead S J, Barcellos L F, Ravindrarajah R, Abraham R, Alfredsson L, Ardlie K, Aubin C, Baker A, Baker K, Baranzini S E, Bergamaschi L, Bergamaschi R, Bernstein A, Berthele A, Boggild M, Bradfield J P, Brassat D, Broadley S A, Buck D, Butzkueven H, Capra R, Carroll W M, Cavalla P, Celius E G, Cepok S, Chiavacci R, Clerget-Darpoux F, Clysters K, Comi G, Cossburn M, Cournu-Rebeix I, Cox M B, Cozen W, Cree B A C, Cross A H, Cusi D, Daly M J, Davis E, de Bakker P I W, Debouverie M, D'Hooghe M B, Dixon K, Dobosi R, Dubois B, Ellinghaus D, Elovaara I, Esposito F, Fontenille C, Foote S, Franke A, Galimberti D, Ghezzi A, Glessner J, Gomez R, Gout O, Graham C, Grant S F A, Guerini F R, Hakonarson H, Hall P, Hamsten A, Hartung H P, Heard R N, Heath S, Hobart J, Hoshi M, Infante-Duarte C, Ingram G, Ingram W, Islam T, Jagodic M, Kabesch M, Kermode A G, Kilpatrick T J, Kim C, Klopp N, Koivisto K, Larsson M, Lathrop M, Lechner-Scott J S, Leone M A, Leppa V, Liljedahl U, Bomfim I L, Lincoln R R, Link J, Liu J J, Lorentzen A R, Lupoli S, Macciardi F, Mack T, Marriott M, Martinelli V, Mason D, McCauley J L, Mentch F, Mero I L, Mihalova T, Montalban X, Mottershead J, Myhr K M, Naldi P, Ollier W, Page A, Palotie A, Pelletier J, Piccio L, Pickersgill T, Piehl F, Pobywajlo S, Quach H L, Ramsay P P, Reunanen M, Reynolds R, Rioux J, Rodegher M, Roesner S, Rubio J P, Ruckert I M, Salvetti M, Salvi E, Santaniello A, Schaefer C A, Schreiber S, Schulze C, Scott R J, Sellebjerg F, Selmaj K W, Sexton D, Shen L, Simms-Acuna B, Skidmore S, Sleiman P M A, Smestad C, Sorensen P S, Sondergaard H B, Stankovich J, Strange R C, Sulonen A M, Sundqvist E, Syvanen A C, Taddeo F, Taylor B, Blackwell J M, Tienari P, Bramon E, Tourbah A, Brown M A, Tronczynska E, Casas J P, Tubridy N, Corvin A, Vickery J, Jankowski J, Villoslada P, Markus H S, Wang K, Mathew C G, Wason J, Palmer C N A, Wichmann H E, Plomin R, Willoughby E, Rautanen A, Winkelmann J, Wittig M, Trembath R C, Yaouanq J, Viswanathan A C, Zhang H T, Wood N W, Zuvich R, Deloukas P, Langford C, Duncanson A, Oksenberg J R, Pericak-Vance M A, Haines J L, Olsson T, Hillert J, Ivinson A J, De Jager P L, Peltonen L, Stewart G J, Hafler D A, Hauser S L, McVean G, Donnelly P, Compston A, Int Multiple Sclerosis Genetics Co, Wellcome Trust Case Control Consor
Revue
InstitutIG
Année2 011

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