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Showing articles 0 to 10 of 10 Filter Applied: inclusion bodies (Click to remove) Clinicopath Conf Dementia with Lewy Bodies, Anaplastic Astrocytoma of Right Insular Region, Case 7-1998, NEJM 338:603, 61098., 1998 Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease NEJM 383:2666-2675, Case 41-2020, 2020 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 Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy JNNP 85:354-356, Sone, J.,et al, 2014 Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis NEJM 364:1062-1074, Case 8-2011, 2011 A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder Neurol 72:1607-1613, Lossos,A.,et al, 2009 Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene Arch Neurol 65:19-25, Amiri,K.,et al, 2008 Clinicopath Conf, Multiple-System Atrophy NEJM 351:912-921, Case 27-2004, 2004 Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy Ann Neurol 27:103-106, Goutieres,F.,et al, 1990 Showing articles 0 to 10 of 10