Showing results (31-40 of 37) with videos related to
Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Neurology|January 19, 2011
Oculopharyngodistal myopathy is a distinct entity: clinical and genetic features of 47 patientsH Durmus, S H Laval, F Deymeer, et al.Neuromuscular Disorders : NMD|August 25, 2019
Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counselingG Toksoy, H Durmus, A Aghayev, et al.Neurology|September 25, 1999
Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit geneL Middleton, K Ohno, K Christodoulou, et al.Cell|May 24, 2001
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndromeN M Plaster, R Tawil, M Tristani-Firouzi, 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 4