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Showing articles 0 to 10 of 10 Filter Applied: Hallervorden Spatz disease (Click to remove) Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Hallervorden-Spatz Syndrome and Brain Iron Metabolism Arch Neurol 48:1285-1293, Swaiman,K.F., 1991 MR Imaging of a Group I Case of Hallervorden-Spatz Disease J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988 Neurodegeneration with Brain Iron Accumulation AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019 Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome NEJM 348:33-40, Hayflick,S.J.,et al, 2003 Diagnostic Approach in Patients with Symmetric Imaging Lesions of the Deep Gray Nuclei The Neurologist 9:250-261, Finelli,P.F.&DiMario,Jr,F.J., 2003 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 Computed tomography in Hallervorden-Spatz disease Neurol 30:1128-1130, Dooling,E.C.,et al, 1980 Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features Ann Neurol 3:419, Dorfman,L.J.,et al, 1978 Showing articles 0 to 10 of 10