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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
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Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
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Transient swelling in the globus pallidus and substantia nigra in childhood suggests SENDA/BPAN
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A Parkinsonian Syndrome in Methcathinone Users and the Role of Manganese
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Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
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Cerebrotendinous Xanthomatosis:Clinical and MRI Study (A Case Report)
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Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
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Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
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Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
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Familial Chorea & Myoclonus Epilepsy
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