Clinical characteristics of familial and sporadic Creutzfeldt-Jakob disease in Finland
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.1993.tb04139.x/fullpdf
Reference38 articles.
1. Descriptive epidemiology of Creutzfeldt-Jakob disease in Finland;KOVANEN;Acta Neurol Scand,1988
2. Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering;MASTERS;Ann Neurol,1979
3. Creutzfeldt-Jakob disease in France: III. Epidemiological study of 170 patients dying during the decade 1968-1977;BROWN;Ann Neurol,1979
4. Familial Creutzfeldt-Jakob disease;HALTIA;J Neurol Sci,1979
5. New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred;GOLDFARB;Lancet,1991
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1. Adult-Onset Neuroepidemiology in Finland: Lessons to Learn and Work to Do;Journal of Clinical Medicine;2023-06-11
2. Isolated language impairment as the primary presentation of sporadic Creutzfeldt Jakob Disease;Acta Neurologica Scandinavica;2016-04-12
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