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Showing articles 0 to 11 of 11 Filter Applied: inclusion bodies (Click to remove) 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 A 42-year-old man with unilateral leg weakness Neurol 90:e1085-e1090, Schneider, R.,et al, 2018 Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018 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 Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9 Ann Neurol 41:432-437, Ikeuchi,T.,et al, 1997 Inclusion Body Myositis JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996 Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy Ann Neurol 27:103-106, Goutieres,F.,et al, 1990 Spectrum of Inclusion Body Myositis Arch Neurol 44:1154-1157, Ringel,S.P.,et al, 1987 Showing articles 0 to 11 of 11