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Showing articles 0 to 11 of 11 Filter Applied: Hallervorden Spatz disease (Click to remove) Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Pantothenate Kinase - Associated Neurodegeneration (PKAN) Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018 Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome NEJM 348:33-40, Hayflick,S.J.,et al, 2003 Hallervorden-Spatz Syndrome and Brain Iron Metabolism Arch Neurol 48:1285-1293, Swaiman,K.F., 1991 Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease Neurol 39:440-442, Schaffert,D.A.,et al, 1989 MR Imaging of a Group I Case of Hallervorden-Spatz Disease J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988 Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988 Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome Neurol 38:154-155, Tennison,M.B.,et al, 1988 MR Imaging in a Case of Hallervorden-Spatz Disease J Comput Assist Tomogr 11:1057-1058, Tanfani,G.,et al, 1987 Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism Neurol 35:227-234, Jankovic,J.,et al, 1985 Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features Ann Neurol 3:419, Dorfman,L.J.,et al, 1978 Showing articles 0 to 11 of 11