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Acta Neuropathologica Communications|March 24, 2017
Calcium dysregulation, functional calpainopathy, and endoplasmic reticulum stress in sporadic inclusion body myositisDavid R Amici, Iago Pinal-Fernandez, Davi A G Mázala, et al.
Rheumatology (Oxford, England)|June 27, 2021
Prevalence of avascular necrosis in idiopathic inflammatory myopathies: a single-centre experienceKhalil I Bourji, Christopher A Mecoli, Julie J Paik, et al.
Arthritis Care & Research|May 20, 2015
Spectrum of Muscle Histopathologic Findings in Forty-Two Scleroderma Patients With WeaknessJulie J Paik, Fredrick M Wigley, Thomas E Lloyd, et al.
Rheumatology (Oxford, England)|January 19, 2017
More severe disease and slower recovery in younger patients with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase-associated autoimmune myopathyEleni Tiniakou, Iago Pinal-Fernandez, Thomas E Lloyd, et al.
Arthritis Care & Research|April 21, 2015
Cytosolic 5'-Nucleotidase 1A As a Target of Circulating Autoantibodies in Autoimmune DiseasesThomas E Lloyd, Lisa Christopher-Stine, Iago Pinal-Fernandez, et al.
Annals of Neurology|January 6, 2025
Loss of TDP-43 Splicing Repression Occurs in Myonuclei of Inclusion Body Myositis PatientsChiseko Ikenaga, Andrew B Wilson, Katherine E Irwin, et al.
Annals of Neurology|January 22, 2022
Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body MyositisChiseko Ikenaga, Hidetoshi Date, Motoi Kanagawa, et al.
Clinical and Experimental Rheumatology|September 8, 2020
Accumulation of autophagosome cargo protein p62 is common in idiopathic inflammatory myopathiesJose C Milisenda, Iago Pinal-Fernandez, Thomas E Lloyd, et al.
Molecular Neurodegeneration|February 4, 2017
Tdp-43 cryptic exons are highly variable between cell typesYun Ha Jeong, Jonathan P Ling, Sophie Z Lin, et al.
Nature Communications|March 5, 2021
Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extensionBrett A McCray, Erika Diehl, Jeremy M Sullivan, et al.
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