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Genetics of inclusion-body myositis.
Needham M, Mastaglia FL, Garlepp MJ. Needham M, et al. Muscle Nerve. 2007 May;35(5):549-61. doi: 10.1002/mus.20766. Muscle Nerve. 2007. PMID: 17366591 Review.
High-resolution HLA-DRB1 genotyping in an Australian inclusion body myositis (s-IBM) cohort: an analysis of disease-associated alleles and diplotypes.
Rojana-udomsart A, James I, Castley A, Needham M, Scott A, Day T, Kiers L, Corbett A, Sue C, Witt C, Martinez P, Christiansen F, Mastaglia F. Rojana-udomsart A, et al. Among authors: needham m. J Neuroimmunol. 2012 Sep 15;250(1-2):77-82. doi: 10.1016/j.jneuroim.2012.05.003. Epub 2012 May 26. J Neuroimmunol. 2012. PMID: 22633068
Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptoms.
Mastaglia FL, Rojana-udomsart A, James I, Needham M, Day TJ, Kiers L, Corbett JA, Saunders AM, Lutz MW, Roses AD; Alzheimer’s Disease Neuroimaging Initiative. Mastaglia FL, et al. Among authors: needham m. Neuromuscul Disord. 2013 Dec;23(12):969-74. doi: 10.1016/j.nmd.2013.09.008. Epub 2013 Sep 19. Neuromuscul Disord. 2013. PMID: 24103330
485 results