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Showing articles 0 to 8 of 8 Filter Applied: retinopathy (Click to remove) A Familial Syndrome of Dystonia, Blepharospasm, and Pigmentary Retinopathy Neurol 40:1359-1363, Coppeto,J.R.&Lessel,S., 1990 Behcet Disease emedicine.medscape.com Dec, Davey-Ranasinghe, N. & Diamond, H.S., 2018 Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome NEJM 348:33-40, Hayflick,S.J.,et al, 2003 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992 Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992 Cockayne Syndrome: Review of 140 Cases Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992 Central Nervous System Manifestations of Periarteritis Nodosa Neurol 15:114, Ford,R.G.,et al, 1965 Showing articles 0 to 8 of 8