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Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
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Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
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Rapidly Progressive Corticobasal Degeneration Syndrome
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Pathologic Correlates of Diffusion MRI Changes in Creutzfeldt-Jakob Disease
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Sporadic Creutzfeldt-Jakob Disease in Two Adolescents
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Pyramidal Tract Degeneration in Sporadic Creutzfeldt-Jakob Disease
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Diagnosing Variant Creutzfeldt-Jakob Disease with the Pulvinar Sign:"MR Imaging Findings in 86 Neuropathologically Confirmed Cases
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Neurodegenerative Diseases and Prions
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Diagnosis of New Variant Creutzfeldt-Jakob Disease
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The Heidenhain Variant of Creutzfeldt-Jakob Disease
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The Risk of Bovine Spongiform Encephalopathy ('Mad Cow Disease') to Human Health
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New Variant Creutzfeldt-Jakob Disease:Neurological Features and Diagnostic Tests
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Bovine Spongiform Encephalopathy and Creutzfeldt-Jakob Disease
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A New Variant of Creutzfeldt-Jakob Disease in the UK
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Posterior Cortical Atrophy:Neuropathologic Correlations
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Transmission of Alpers'Disease (Chr Prog Encephalopathy) Produces Exper Creutzfeldt-Jakob Disease in Hamsters
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Creutzfeldt-Jakob Disease:Correlation of MRI & Neuropathologic Findings
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Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)
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Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
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Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
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Zika Virus Associated with Microcephaly
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Diagnosis and Misdiagnosis of Adult Neuronal Ceroid Lipofuscinosis
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
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A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis
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Degenerative Diseases of the Nervous System, Alzheimer Disease
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Clinicopath Conf, Infantile Krabbe Disease
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Clinical and Neuroimaging Findings of Cree Leukodystrophy: A Retrospective Case Series
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Parkinsons Disease
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Aicardi-Gouti�res Syndrome
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Clinical Features and Neuropathology of Autosomal Dominant Spinocerebellar Ataxia (SCA17)
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Familial Dementia With Lewy Bodies
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Familial Infantile Bilateral Striatal Necrosis
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Autosomal Dominant Diffuse Leukoencephalopathy with Neuroaxonal Spheroids
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Multiple Sclerosis
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Hereditary Form of Parkinsonism-Dementia
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