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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 Triad of Tremor, Ataxia, and Cognitive Impairment Neurol 96:e1802-e1803, Au, L.W.C.,et al, 2021 A 65-Year-Old Woman with Tremor Neurol 97:e1257-e1261, Ye, J.,et al, 2021 Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis NEJM 364:1062-1074, Case 8-2011, 2011 Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene Arch Neurol 65:19-25, Amiri,K.,et al, 2008 Fragile X Premutation With Atypical Symptoms at Onset Arch Neurol 63:1135-1138, Cellini,E.,et al, 2006 Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy Ann Neurol 27:103-106, Goutieres,F.,et al, 1990 Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger Ann Neurol 2:473, deLeon,G.A.,et al, 1977 Showing articles 0 to 8 of 8