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Showing articles 0 to 14 of 14 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 Progressive Proximal Weakness in a 56-year-old Man with Bone Pain Neurol 93:939-944, Torabi,T.,et al, 2019 Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy JNNP 85:354-356, Sone, J.,et al, 2014 Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis NEJM 364:1062-1074, Case 8-2011, 2011 A 23-Year-Old Man With Seizures and Visual Deficit Neurol 70:73-78, Boustany,R.-M.,et al, 2008 Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1 Ann Neurol 41:548-551, Argov,Z.,et al, 1997 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 Inclusion Body Myositis and Myopathies Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995 Treatment of Inclusion-Body Myositis with High-Dose Intravenous Immunoglobulin Neurol 43:876-879, Soueidan,S.A.&Dalakas,M.C., 1993 Spectrum of Inclusion Body Myositis Arch Neurol 44:1154-1157, Ringel,S.P.,et al, 1987 Inclusion Body Myositis Arch Neurol 39:760-764, Danon,M.J.,et al, 1982 Human-To-Human Transmission of Rabies Virus by Corneal Transplant NEJM 300:603-604, Houff,S.A.,et al, 1979 Polyradiculoneuropathy in Addison's Disease:Case report & review of literature Neurol 27:494, Abbas,D.H.,et al, 1977 Showing articles 0 to 14 of 14