Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
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Glucose Hypermetabolism in the Basal Ganglia
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Antibody-Mediated Encephalitis
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Pyruvate Dehydrogenase Deficiency (PDCD)
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Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
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Clinicopathologic Conference, Blind and Confused, Neuromyelitis Optica Spectrum Disorder
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Subacute Sclerosing Panencephalitis
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Cognitive Delay in a 7-year-old Girl
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Pediatric Neurological Complications of 2009 Pandemic Influenza A (H1N1)
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Predicting motor outcome and death in term hypoxic-ischemic encephalopathy
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Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
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Epilepsy in Children with Infantile Thiamine Deficiency
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A 23-Year-Old Man With Seizures and Visual Deficit
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Neuroimaging Findings in Human Prion Disease
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Creutzfeldt-Jakob Disease: Comparative Analysis of MR Imaging Sequences
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West Nile Virus Neuroinvasive Disease
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Neurologic Manifestations in Welders with Pallidal MRI T1 Hyperintensity
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Neuropsychiatry of the Basal Ganglia
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Out of Africa, Trypanosomiasis
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T2 Hypointensity in the Deep Gray Matter of Patients With Multiple Sclerosis
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De Novo Mutation in the Notch3 Gene Causing CADASIL
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Retinocochleocerebral Vasculopathy
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Susac Syndrome
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Neurologic Outcomes in Children with Post-Pump Choreoathetosis
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Neuroimaging Findings in Late Infantile GM1 Gangliosidosis
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Bilirubin Metabolism and Kernicterus
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Adult-Onset Subacute Sclerosing Panecephalitis:Case Reports and Review of the Literature
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Persistence of MRI Hyperintensity of the Globus Pallidus in Cirrhotic Patients:A 2-year Follow-up Study
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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
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Neurological Sequelae of Cyanide Intoxication-The Patterns of Clinical MRI & Pet Findings
Ann Neurol 38:825-828, Rosenow,F.,et al, 1995
Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Neurobehavioral Changes Associated with Caudate Lesions
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Reversibility of CT and MR Findings in Neuro-Bechet Disease
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Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
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Neurological Syndrome Following Bilateral Damage to the Head of the Caudate Nuclei
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Infantile Bilateral Striatal Necrosis, Clinicopathological Classification
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Pure Psychic Akinesia with Bilateral Lesions of Basal Ganglia
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