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Showing articles 0 to 8 of 8 Filter Applied: inclusion bodies (Click to remove) Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018 A 60-Year-Old Man with Weakness and Gait Dysfunction JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025 Progressive Proximal Weakness in a 56-year-old Man with Bone Pain Neurol 93:939-944, Torabi,T.,et al, 2019 Intractable Epilepsy and Progressive Cognitive Decline in a Young Man JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017 Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism NEJM 372:1151-1162, Miller, B.L.,et al, 2015 Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1 Ann Neurol 41:548-551, Argov,Z.,et al, 1997 Treatment of Inclusion-Body Myositis with High-Dose Intravenous Immunoglobulin Neurol 43:876-879, Soueidan,S.A.&Dalakas,M.C., 1993 Case Records of MGH-NEJM 286:1047 1972 Progressive Multifocal Leukoencephalopathy., , 1972 Showing articles 0 to 8 of 8