Accumulation of prion protein in the vagus nerve in creutzfeldt–jakob disease-Reference-Cited by-同舟云学术

Accumulation of prion protein in the vagus nerve in creutzfeldt–jakob disease

Published:2019-03-11 Issue:5 Volume:85 Page:782-787
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol

Author:

Kresl Philip¹²,Rahimi Jasmin³,Gelpi Ellen¹²⁴,Aldecoa Iban⁴,Ricken Gerda¹,Danics Krisztina⁵,Keller Eva⁵,Kovacs Gabor G.¹²⁵

Affiliation:

1. Institute of NeurologyMedical University of Vienna Vienna Austria

2. Austrian Reference Center for Human Prion DiseasesMedical University of Vienna Vienna Austria

3. Department of Neurology and Karl Landsteiner Institute for Neuroimmunological and Neurodegenerative DisordersDanube Hospital Vienna Austria

4. Neurological Tissue Bank, Biobanc Hospital Clinic, August Pi i Sunyer Biomedical Research Institute, and Pathology Department, Biomedical Diagnostic CenterBarcelona Hospital Clinic Barcelona Spain

5. Neuropathology and Prion Disease Reference Center, Department of Forensic and Insurance MedicineSemmelweis University Budapest Hungary

Funder

Federal Ministry of Labour, Social Affairs, Health and Consumer Protection

Medizinisch-Wissenschaftlichen Fonds des Bürgermeisters der Stadt Wien

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.25451

Reference24 articles.

1. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

2. Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

3. Neuropathologic characteristics of brainstem lesions in sporadic Creutzfeldt-Jakob disease

4. PrPCWD in the myenteric plexus, vagosympathetic trunk and endocrine glands of deer with chronic wasting disease

5. TSE pathogenesis in cattle and sheep

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