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Showing articles 0 to 8 of 8 Filter Applied: inclusion bodies (Click to remove) Human-To-Human Transmission of Rabies Virus by Corneal Transplant NEJM 300:603-604, Houff,S.A.,et al, 1979 A 60-Year-Old Man with Weakness and Gait Dysfunction JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025 Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen NEJM 376:158-167, Case 1-2017, 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 Infantile Gaucher's Disease:A Case with Neuronal Storage Ann Neurol 23:300-303, Grafe,M.,et al, 1988 Spectrum of Inclusion Body Myositis Arch Neurol 44:1154-1157, Ringel,S.P.,et al, 1987 Classic & Generalized Variants of Pick's Disease, A Clinicopath, Ultrastruc & Immunocyto Study Ann Neurol 16:467-480, Munoz-Garcia,D.,et al, 1984 Case Records of MGH-NEJM 286:1047 1972 Progressive Multifocal Leukoencephalopathy., , 1972 Showing articles 0 to 8 of 8