Browse by People

Collapse authors list.
Rothwell, Simon, Cooper, Robert G ORCID: 0000-0001-8337-9973, Lundberg, Ingrid E, Gregersen, Peter K, Hanna, Michael G, Machado, Pedro M, Herbert, Megan K, Pruijn, Ger JM, Lilleker, James B, Roberts, Mark et al (show 22 more authors) , Bowes, John, Seldin, Michael F, Vencovsky, Jiri, Danko, Katalin, Limaye, Vidya, Selva-O'Callaghan, Albert, Platt, Hazel, Molberg, Oyvind, Benveniste, Olivier, Radstake, Timothy RDJ, Doria, Andrea, De Bleecker, Jan, De Paepe, Boel, Gieger, Christian, Meitinger, Thomas, Winkelmann, Juliane, Amos, Christopher I, Ollier, William E, Padyukov, Leonid, Lee, Annette T, Lamb, Janine A and Chinoy, Hector (2017) Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis Spectrum. ARTHRITIS & RHEUMATOLOGY, 69 (5). pp. 1090-1099.

Collapse authors list.
Gang, Qiang, Bettencourt, Conceição, Machado, Pedro M, Brady, Stefen, Holton, Janice L, Pittman, Alan M ORCID: 0000-0002-8112-2987, Hughes, Deborah, Healy, Estelle, Parton, Matthew, Hilton-Jones, David et al (show 20 more authors) , Shieh, Perry B, Needham, Merrilee, Liang, Christina, Zanoteli, Edmar, de Camargo, Leonardo Valente, De Paepe, Boel, De Bleecker, Jan, Shaibani, Aziz, Ripolone, Michela, Violano, Raffaella, Moggio, Maurizio, Barohn, Richard J, Dimachkie, Mazen M, Mora, Marina, Mantegazza, Renato, Zanotti, Simona, Singleton, Andrew B, Hanna, Michael G, Houlden, Henry and Muscle Study Group and The International IBM Genetics Consortium, (2016) Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis. Neurobiology of aging, 47. 218.e1-218.e9.