Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
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Carbamazepine Encephalopathy Masquerading as Creutzfeldt-Jakob Disease
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Diffusion-Weighted MR Imaging of the Brain
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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
Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024
Long Survival Sporadic Creutzfeldt-Jakob Disease
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Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
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Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure
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An Atypical Presentation of Creutzfeldt-Jakob Disease with a Heidenhain Variant and Balints Syndrome
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A 64-year-old Man with Visual Distortions
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Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
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Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UK
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Sporadic Creutzfeldt-Jakob Disease Mimicking Nonconvulsive Status Epilepticus
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Bilateral Thalamic Lesions
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Transmissible Spongiform Encephalopathy in the 21st Century: Neuroscience for the Clinical Neurologist
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Differential Diagnosis of Restricted Diffusion Confined to the Cerebral Cortex
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Sleep-wake Disturbances in Sporadic Creutzfeldt-Jakob Disease
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Onset of Creutzfeldt-Jakob Disease Mimicking an Acute Cerebrovascular Event
Neurol 67:538-539, Hohler,A.D. &Flynn,F.G., 2006
Diffusion-Weighted MRI Abnormalities as an Early Diagnostic Marker for Creutzfeldt-Jakob Disease
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Antivonvulsants for Creutzfeldt-Jakob Disease?
Lancet 361:224, Fioel,A.,et al, 2003
Generalized Convulsive Status Epilepticus in Creutzfeldt-Jakob Disease
Seizure 12:403-406, Neufeld,M.Y.,et al, 2003
Current Clinical Diagnosis in Creutzfeldt-Jakob Disease; Identification of Uncommon Variants
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Analysis of EEG and CSF 14-3-3 proteins as adis to the diagnosis of Creutzfeldt-Jakob Disease
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Progressive Aphasia with Rapidly Progressive Dementia in a 49 Year Old Woman
JNNP 66:238-243, Greene,J.D.W.,et al,, 1999
Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999
Surgical Treatment and Risk of Sporadic Creutzfeldt-Jakob Disease:A Case-Control Study
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Mortality from Dementia in Occupations at Risk of Exposure to Bovine Spongiform EncephalopathyAnalysis of Death Registrations
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Seizures and Creutzfeldt-Jakob Disease
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Creutzfeldt-Jakob Disease Presenting as Complex Partial Status Epilepticus: A Report of Two Cases
JNNP 66:406-407, Rees,J.H.,et al, 1999
Case-Control Study of Risk Factors of Creutzfeldt-Jacob Disease in Europe During 1993-95
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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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Transmissible Spongiform Encephalopathies
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Accuracy and Reliability of Periodic Sharp Wave Complexes in Creutzfeldt-Jakob Disease
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A New Variant of Creutzfeldt-Jakob Disease in the UK
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The 14-3-3 Brain Protein in Cerebrospinal Fluid as a Marker for Transmissible Spongiform Encephalopathies
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Creutzfeldt-Jakob Disease and Bovine Spongiform Encephalopathy:Any Connection?
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Creutzfeldt-Jakob Disease in a Physician:A Review of the Disorder in Health Care Workers
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Creutzfeldt-Jakob Disease in a Pathologist
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Protein Processing in Lysosomes:The New Therapeutic Target in Neurodegenerative Disease
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Demonstration of the Transmissible Agent in Tissue From a Pregnant Woman with Creutzfeldt-Jakob Disease
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"Friendly Fire"in Medicine:Hormones, Homografts, and Creutzfeldt-Jakob Disease
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Drug Induced Creutzfeldt-Jakob Like Syndrome
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Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
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Creutzfeldt-Jakob Disease and Other Transmissible Spongiform Encephalopathies
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Familial Creutzfeldt-Jakob Disease without Periodic EEG Activity
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