Parkinson's Disease
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A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025
Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
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Clinicopathologic Conference,Aceruloplasminemia, Hereditary
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Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
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Clinicopathologic Conference, Creutzfeldt-Jakob Disease
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Antibody-Mediated Encephalitis
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Huntington Disease: Clinical Features and Diagnosis
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Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
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A 23-Year-Old Man With Seizures and Visual Deficit
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Neuroimaging Findings in Human Prion Disease
JNNP 78:664-670, Macfarlane,R.G.,et al, 2007
Creutzfeldt-Jakob Disease: Comparative Analysis of MR Imaging Sequences
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Subacute Sclerosing Panencephalitis
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Chorea Resulting From Paraneoplastic Striatal Encephalitis
JNNP 69:512-515, Tani,T.,et al, 2000
De Novo Mutation in the Notch3 Gene Causing CADASIL
Ann Neurol 47:388-391, Joutel,A.,et al, 2000
Retinocochleocerebral Vasculopathy
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Susac Syndrome
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Adult-Onset Subacute Sclerosing Panecephalitis:Case Reports and Review of the Literature
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Clinical Spectrum of CADASIL:A Study of 7 Families
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New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
JNNP 59:579-585, Verin,M.,et al, 1995
Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Cerebrotendinous Xanthomatosis:Clinical and MRI Study (A Case Report)
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Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease
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Reversibility of CT and MR Findings in Neuro-Bechet Disease
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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
Neurol 38:1065-1070, Takahashi,H.,et al, 1988
Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
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Alcoholic Dementia:A Hypothesis
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Pathologic Correlates of Dementia in Parkinson's Disease
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The Nucleus Basalis of Meynert in Neurological Disease:A Quantitative Morphological Study
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Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
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Familial Chorea & Myoclonus Epilepsy
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