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A novel homozygous missense mutation in the GNE gene of a patient with quadriceps-sparing hereditary inclusion body myopathy associated with muscle inflammation.
Krause S, Schlotter-Weigel B, Walter MC, Najmabadi H, Wiendl H, Müller-Höcker J, Müller-Felber W, Pongratz D, Lochmüller H. Krause S, et al. Among authors: Wiendl H. Neuromuscul Disord. 2003 Dec;13(10):830-4. doi: 10.1016/s0960-8966(03)00140-8. Neuromuscul Disord. 2003. PMID: 14678807
HLA-G in the nervous system.
Wiendl H. Wiendl H. Hum Immunol. 2007 Apr;68(4):286-93. doi: 10.1016/j.humimm.2006.10.021. Epub 2006 Dec 8. Hum Immunol. 2007. PMID: 17400065 Review.
FOXP3+ T regulatory cells in idiopathic inflammatory myopathies.
Waschbisch A, Schwab N, Ruck T, Stenner MP, Wiendl H. Waschbisch A, et al. Among authors: Wiendl H. J Neuroimmunol. 2010 Aug 25;225(1-2):137-42. doi: 10.1016/j.jneuroim.2010.03.013. J Neuroimmunol. 2010. PMID: 20537411
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