Accuracy and Reliability of Periodic Sharp Wave Complexes in Creutzfeldt-Jakob Disease
Arch Neurol 53:162-166, Steinhoff,B.J.,et al, 1996
A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996
MRI of Creutzfeldt-Jakob Disease:Asymmetric High Signal Intensity of the Basal Ganglia
Neurol 45:1932-1933, Yoon,S.S.,et al, 1995
Creutzfeldt-Jakob Disease after Liver Transplantation
Ann Neurol 38:269-272, Creange,A.,et al, 1995
Lyme Neuroborreliosis
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Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
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Management of Acoustic Neuroma
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Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994
The Apolipoprotein E Alleles as Major Susceptibility Factors for Creutzfeldt-Jakob Disease
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MR Diagnosis of Creutzfeldt-Jakob Disease:Significance of High Signal Intensity of the Basal Ganglia
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Iatrogenic Creutzfeldt-Jakob Disease:An Example of the Interplay Between Ancient Genes and Modern Medicine
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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 and Blood Transfusion
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Positron Emission Tomographjy and Histopathology in Creutzfeldt-Jakob Disease
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MRI Abnormalities in Creutzfeldt-Jakob Disease
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Serum anti-GQ1b IgG antibody is Associated with Ophthalmoplegia in Miller Fisher Syndrome and Guillain-Barre Syndrome: Clinical and Immunohistochemical Studies
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The Use of Magnetic Resonance Imaging in Diagnosing Infantile Neuroaxonal Dystrophy
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Creutzfeldt-Jakob Disease in a Recipient of Human Pituitary-Derived Gonadotrophin:A Second Case
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Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
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Drug Induced Creutzfeldt-Jakob Like Syndrome
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Evaluation of Cerebral Biopsies for the Diagnosis of Dementia
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Creutzfeldt-Jakob Disease in a Pathologist
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Chiari I Malformations:Clinical and Radiologic Reappraisal
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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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Serial MR Imaging in Creutzfeldt-Jakob Disease
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Genetic Predisposition to Iatrogenic Creutzfeldt-Jakob Disease
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Creutzfeldt-Jakob Disease in a Patient with a Cadaveric Dural Graft
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Dementia Presenting with Aphasia:Clinical Characteristics
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Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991
Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
NEJM 324:1091-1097, Hsiao,K.,et al, 1991
Mortality, Neoplasia, & Creutzfeldt-Jakob Disease in Patients Treated with Human Pituitary Growth Hormone in the UK
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Creutzfeldt-Jakob Disease and Other Transmissible Spongiform Encephalopathies
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Creutzfeldt-Jakob Disease in Pituitary Growth Hormone Recipients in the United States
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CT Appearance of Panencephalopathic and Ataxic Type of Creutzfeldt-Jakob Disease
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Magnetic Resonance Imaging of Creutzfeldt-Jakob Disease
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Familial Creutzfeldt-Jakob Disease without Periodic EEG Activity
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A Simple & Effective Method for Inactivating Virus Infectivity from Patients with Creutzfeldt-Jakob Disease
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Positron Emission Tomography in Creutzfeldt-Jakob Disease
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Miller Fisher Syndrome Associated with Q Fever
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Rapid Detection of Creutzfeldt-Jakob Disease and Scrapie Prion Porteins
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