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Showing articles 0 to 11 of 11 Filter Applied: inclusion bodies (Click to remove) Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy Ann Neurol 27:103-106, Goutieres,F.,et al, 1990 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 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 Fragile X Premutation With Atypical Symptoms at Onset Arch Neurol 63:1135-1138, Cellini,E.,et al, 2006 Inclusion Body Myositis JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996 Abnormalties In Cultured Muscle & Periphral Nerve Of A Patient With Adrenomyeloneuropathy NEJM 301:588-590, Askanas,V.,et al, 1979 Showing articles 0 to 11 of 11