Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
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Creutzfeldt-Jakob Disease in a Young Woman
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Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
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Precipitous Deterioration of Motor Function, Cognition, and Behavior
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Voltage-Gated Potassium Channel Autoimmunity Mimicking Creutzfeldt-Jakob Disease
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Clinicopath conf., Human Prion Disease, Sporadic CJD
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Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
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Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
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Drug Induced Creutzfeldt-Jakob Like Syndrome
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Creutzfeldt-Jakob Disease and Other Transmissible Spongiform Encephalopathies
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A Creutzfeldt-Jakob Like Syndrome Due to Lithium Toxicity
JNNP 51:120-123, Smith,S.J.M.&Kocen,R.S., 1988
Creutzfeldt-Jakob Disease without Periodic Sharp Wave Complexes:A Clinical, EEG, and Path Study
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Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
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Creutzfeldt-Jakob Disease:Clinical Analysis of a Consecutive Series of 230 Neuropathologically Verified Cases
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Creutzfeldt-Jakob Disease of Long Duration:Clinicopathological Characteristics
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Creutzfeldt-Jakob Disease in a 20-year-old Woman
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Clinical Similarity of Alzheimer & Creutzfeldt-Jakob Disease
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Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)
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Clinical Picture in Creutzfeldt-Jakob Disease
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Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
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Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
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Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
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Neuroimaging Changes in Menkes Disease, Part 1
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A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
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Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis
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A 27-Year Old Man with Rapidly Progressive Coma
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Progressive Gait Deterioration in Adolescents with Dravet Syndrome
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Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
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Whipples Disease
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Wilson Disease: Description of 282 Patients Evaluated Over 3 Decades
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Epilepsy Syndromes in Infancy
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
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Localization of a Gene for Myoclonus-Dystonia to Chromosome 7q21-q31
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Clinical and Genetic Studies of Fatal Familial Insomnia
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