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Showing articles 0 to 12 of 12 Filter Applied: retinopathy (Click to remove) Clinicopathologic Conference,Aceruloplasminemia, Hereditary NEJM 383:1974-1983, Case 35-2020, 2020 Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome NEJM 348:33-40, Hayflick,S.J.,et al, 2003 Retinocochleocerebral Vasculopathy Medicine 77:12-40, Petty,G.W.,et al, 1998 Susac Syndrome Medicine 77:3-11, Papo,T.,et al, 1998 Mucolipidosis Type IV; Characteristic MRI Findings Neurol 51:565-569, Frei,K.P.,et al, 1998 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 Microangiopathy of the Brain, Retina, and Ear:Improvement without Immunosuppressive Therapy Stroke 22:933-937, Gordon,D.L.,et al, 1991 Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Pseudoxanthoma Elasticum:A Review of Neurological Complications Ann Neurol 4:18, Iqbal,A.,et al, 1978 Genetic Counseling in Retinitis Pigmentosa MCV Quart 8:283, Noah,V., 1972 Rubella, Clinical Manifestations & Management Am J Dis Child 118:18-29, Cooper,L.Z.,et al, 1969 Showing articles 0 to 12 of 12