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European Journal of Neurology|May 23, 2008
MuSK-positive myasthenia gravis is rare in the Polish populationA Kostera-Pruszczyk, A Kamińska, M Dutkiewicz, et al.Neurology|March 15, 2006
Charcot-Marie-Tooth type 4F disease caused by S399fsx410 mutation in the PRX geneD Kabzinska, H Drac, D L Sherman, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|April 17, 2002
Clinical, electrophysiological and immunological remissions after thymectomy in myasthenia gravisA Kostera-Pruszczyk, B Emeryk-Szajewska, J Switalska, et al.European Journal of Neurology|January 31, 2026
EAN 2024 Guideline on the Diagnostic Approach to Oligo/Asymptomatic HyperCKemiaT Kyriakides, K Aleksovska, C Angelini, et al.Journal of Autoimmunity|December 31, 2013
A comprehensive analysis of the epidemiology and clinical characteristics of anti-LRP4 in myasthenia gravisP Zisimopoulou, P Evangelakou, J Tzartos, et al.Journal of Neuroimmunology|May 31, 2015
MuSK autoantibodies in myasthenia gravis detected by cell based assay--A multinational studyA I Tsonis, P Zisimopoulou, K Lazaridis, et al.Journal of Neuroimmunology|March 6, 2016
Titin antibodies in "seronegative" myasthenia gravis--A new role for an old antigenC Stergiou, K Lazaridis, V Zouvelou, et al.Pageof 2