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Showing articles 0 to 10 of 10 Filter Applied: inclusion bodies,intranuclear (Click to remove) GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019 Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy JNNP 85:354-356, Sone, J.,et al, 2014 Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene Arch Neurol 65:19-25, Amiri,K.,et al, 2008 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 40-Year-Old Woman Presenting with Distal Leg Weakness Neurol 92:242-247, Fam, D.,et al, 2019 Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018 Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease Neurol 76:1372-1376, Sone, J.,et al, 2011 Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1 Ann Neurol 41:548-551, Argov,Z.,et al, 1997 Inclusion Body Myositis and Myopathies Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995 Showing articles 0 to 10 of 10