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Showing articles 0 to 6 of 6 Filter Applied: iron,brain (Click to remove) Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding Ann Neurol 87:10-11, Van Samkar, A.,et al, 2020 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 Restless Legs Syndrome NEJM 348:2103-2109, Earley,C.J., 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 Showing articles 0 to 6 of 6