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VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravis.
Avidan N, Le Panse R, Harbo HF, Bernasconi P, Poulas K, Ginzburg E, Cavalcante P, Colleoni L, Baggi F, Antozzi C, Truffault F, Horn-Saban S, Pöschel S, Zagoriti Z, Maniaol A, Lie BA, Bernard I, Saoudi A, Illes Z, Casasnovas Pons C, Melms A, Tzartos S, Willcox N, Kostera-Pruszczyk A, Tallaksen C, Mantegazza R, Berrih-Aknin S, Miller A. Avidan N, et al. Ann Clin Transl Neurol. 2014 May;1(5):329-39. doi: 10.1002/acn3.51. Epub 2014 Apr 11. Ann Clin Transl Neurol. 2014. PMID: 25356403 Free PMC article.
Methylome and transcriptome profiling in Myasthenia Gravis monozygotic twins.
Mamrut S, Avidan N, Truffault F, Staun-Ram E, Sharshar T, Eymard B, Frenkian M, Pitha J, de Baets M, Servais L, Berrih-Aknin S, Miller A. Mamrut S, et al. Among authors: avidan n. J Autoimmun. 2017 Aug;82:62-73. doi: 10.1016/j.jaut.2017.05.005. Epub 2017 May 24. J Autoimmun. 2017. PMID: 28549776
Harvesting the human genome: the Israeli perspective.
Ben-Asher E, Chalifa-Caspi V, Horn-Saban S, Avidan N, Olender Z, Adato A, Glusman G, Safran M, Rubinstein M, Lancet D. Ben-Asher E, et al. Among authors: avidan n. Isr Med Assoc J. 2000 Sep;2(9):657-64. Isr Med Assoc J. 2000. PMID: 11062763 Free article.
Translation towards personalized medicine in Multiple Sclerosis.
Miller A, Avidan N, Tzunz-Henig N, Glass-Marmor L, Lejbkowicz I, Pinter RY, Paperna T. Miller A, et al. Among authors: avidan n. J Neurol Sci. 2008 Nov 15;274(1-2):68-75. doi: 10.1016/j.jns.2008.07.028. Epub 2008 Sep 12. J Neurol Sci. 2008. PMID: 18789804 Review.
46 results