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Showing articles 0 to 12 of 12 Filter Applied: inclusion bodies,intranuclear (Click to remove) A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness Neurol 105:e214233, Bu,S.,et al, 2025 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 40-Year-Old Woman Presenting with Distal Leg Weakness Neurol 92:242-247, Fam, D.,et al, 2019 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 Presenile Dementia with Lewy Bodies & Neurofibrillary Tangles Arch Neurol 35:818-822, Forno,L.S.,et al, 1978 Case Records of MGH-NEJM 290:273 1974 Subacute Sclerosing Panencephalitis., , 1974 Case Records of MGH NEJM 29l:l4l, 1974; 29l:263, 1974 Subscute Sclerosing Panencephalitis., , 1974 Showing articles 0 to 12 of 12