Human transmissible spongiform encephalopathies in eleven countries

Diagnostic pattern across time, 1993–2002

Bibliographic Data

ID15379294
AuthorsJesús de Pedro-Cuesta, Jesús de Pedro‐Cuesta (0000-0003-2431-9641, Centro Nacional de Epidemiología, corresponding author), Markus Glatzel (0000-0002-7720-8817, Universität Hamburg), Javier Almazán (Instituto de Salud Carlos III), Katharina Stoeck (University Hospital of Zurich), Vittorio Mellina (Istituto Superiore di Sanità), Maria Puopolo (0000-0001-5410-2334, Istituto Superiore di Sanità), Maurizio Pocchiari (0000-0002-7269-2486, Istituto Superiore di Sanità), Inga Zerr (0000-0002-6722-2463, University of Göttingen), Hans A Kretszchmar (Ludwig-Maximilians-Universität München), Jean‐Philippe Brandel (Sorbonne Université), Jean-Philippe Brandel, N Delasnerie–Lauprêtre (Pitié-Salpêtrière Hospital), Nicole Delasnerie-Lauprêtre, Annick Alpérovitch (Sorbonne Université), Cornelia M Van Duijn (0000-0002-2374-9204, Erasmus University Rotterdam), Cornelia van Duijn, Pascual Sánchez‐Juan (Erasmus University Rotterdam), Pascual Sanchez-Juan, Steven Collins (0000-0002-5245-6611, The University of Melbourne), Victoria Lewis (0009-0006-7253-5903, The University of Melbourne), Gerard H Jansen (0000-0002-4316-7666, Public Health Agency of Canada), Michael B Coulthart (Public Health Agency of Canada), Ellen Gelpi (0000-0003-2948-4187, Medical University of Vienna), Herbert Budka (0000-0002-1933-1577, Medical University of Vienna), Eva Mitrova
Year2006
Volume6
Issue1
Pages278-278
Publication date2006-11-10
Open AccessYes
TypeARTICLE
VenueBMC Public Health (JOURNAL)
Journal identifiersISSN: 1471-2458 • E-ISSN: 1471-2458
PublisherBioMed Central (PUBLISHER • GB)
DOI10.1186/1471-2458-6-278
PMID17096829
PMCIDPMC1665456
OpenAlexW2168744512
LanguageEN
Citations received3
References cited24

Considerable international variation in aetiological subtypes of human transmissible spongiform encephalopathies was evident over the observation period. With the exception of variant Creutzfeldt-Jakob disease and iatrogenic Creutzfeldt-Jakob disease in France and the United Kingdom, these differences persisted across time

Creutzfeldt-Jakob Syndrome · Disease · Etiology · Incidence (geometry · Pathology · Prion protein · Scrapie · Transmissible spongiform encephalopathy · Demography · Medicine · Prion Diseases and Protein Misfolding · Epidemiology · Pediatrics · Virology

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