Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation

Keyphrases

• Codon 100%
• Creutzfeldt-Jakob Disease 100%
• Unusual Presentation 100%
• Clinical Heterogeneity 100%
• Jewish Patients 100%
• Disease Duration 50%
• Brainstem 50%
• Age of Onset 50%
• Basal Ganglia 50%
• Jews 50%
• Ethnic Groups 50%
• Clinical Features 50%
• Protein Precursors 50%
• Libyan 50%
• Clinical Data 50%
• Point mutation 50%
• Prion Protein 50%
• Phenotypic Heterogeneity 50%
• Pruritus 50%
• Fatal Familial Insomnia 50%
• Demyelinating Peripheral Neuropathy 50%
• Spinal Cord Diseases 50%

Biochemistry, Genetics and Molecular Biology

• Codon 100%
• Creutzfeldt-Jakob Disease 100%
• PRNP 100%
• Protein Precursor 50%
• Point Mutation 50%
• Prion 50%
• Phenotypic Heterogeneity 50%