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Journal of Neurology|October 13, 2001
The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated casesV Planté-Bordeneuve, Y Parman, A Guiochon-Mantel, et al.Neurology|February 21, 2007
Clinical comparison of anti-MuSK- vs anti-AChR-positive and seronegative myasthenia gravisF Deymeer, O Gungor-Tuncer, V Yilmaz, et al.Muscle & Nerve|December 1, 1993
Emery-Dreifuss muscular dystrophy with unusual featuresF Deymeer, A E Oge, C Bayindir, et al.Muscle & Nerve|August 14, 1998
The dominant chloride channel mutant G200R causing fluctuating myotonia: clinical findings, electrophysiology, and channel pathologyS Wagner, F Deymeer, L L Kürz, et al.Clinical and Experimental Immunology|April 1, 2019
Relation of HLA-DRB1 to IgG4 autoantibody and cytokine production in muscle-specific tyrosine kinase myasthenia gravis (MuSK-MG)M Çebi, H Durmuş, V Yılmaz, et al.Journal of Neuroimmunology|September 25, 2020
The treatment effect on peripheral B cell markers in antibody positive myasthenia gravis patientsV Yilmaz, E Tuzun, H Durmus, et al.Neurogenetics|August 29, 2001
Mapping of the second Friedreich's ataxia (FRDA2) locus to chromosome 9p23-p11: evidence for further locus heterogeneityK Christodoulou, F Deymeer, P Serdaroğlu, et al.Human Molecular Genetics|April 1, 1997
Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type Ia) gene to chromosome 17p with evidence of genetic homogeneityK Christodoulou, M Tsingis, F Deymeer, et al.Neurology|May 12, 2004
Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second geneN Bissar-Tadmouri, E Nelis, S Züchner, et al.Journal of Medical Genetics|February 1, 1993
Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28J R Yates, J P Warner, J A Smith, et al.Pageof 4