Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease.
Journal
The Lancet. Neurology
ISSN: 1474-4465
Titre abrégé: Lancet Neurol
Pays: England
ID NLM: 101139309
Informations de publication
Date de publication:
03 2021
03 2021
Historique:
received:
10
06
2020
revised:
19
11
2020
accepted:
04
12
2020
pubmed:
21
2
2021
medline:
5
3
2021
entrez:
20
2
2021
Statut:
ppublish
Résumé
Sporadic Creutzfeldt-Jakob disease is a fatal neurodegenerative disease caused by misfolded prion proteins (PrP
Identifiants
pubmed: 33609480
pii: S1474-4422(20)30477-4
doi: 10.1016/S1474-4422(20)30477-4
pmc: PMC8285036
mid: NIHMS1684588
pii:
doi:
Substances chimiques
Biomarkers
0
Genetic Markers
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
235-246Subventions
Organisme : Medical Research Council
ID : MR/J016071/1
Pays : United Kingdom
Organisme : NIA NIH HHS
ID : R56 AG055619
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG031189
Pays : United States
Organisme : Chief Scientist Office
ID : ETM/58
Pays : United Kingdom
Organisme : NIA NIH HHS
ID : R01 AG062562
Pays : United States
Organisme : Medical Research Council
ID : MC_UU_00024/1
Pays : United Kingdom
Organisme : NIA NIH HHS
ID : R01-AG AG031189
Pays : United States
Commentaires et corrections
Type : ErratumIn
Informations de copyright
Copyright © 2021 Elsevier Ltd. All rights reserved.
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