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Page 1
Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease.
Hermann P, Appleby B, Brandel JP, Caughey B, Collins S, Geschwind MD, Green A, Haïk S, Kovacs GG, Ladogana A, Llorens F, Mead S, Nishida N, Pal S, Parchi P, Pocchiari M, Satoh K, Zanusso G, Zerr I. Hermann P, et al. Lancet Neurol. 2021 Mar;20(3):235-246. doi: 10.1016/S1474-4422(20)30477-4. Lancet Neurol. 2021. PMID: 33609480 Free PMC article. Review.
Sporadic Creutzfeldt-Jakob disease is a fatal neurodegenerative disease caused by misfolded prion proteins (PrP(Sc)). ...Development and clinical application of disease-specific protein aggregation and amplification assays, such as real-time qua …
Sporadic Creutzfeldt-Jakob disease is a fatal neurodegenerative disease caused by misfolded prion proteins (PrP( …
Prion Disease.
Baldwin KJ, Correll CM. Baldwin KJ, et al. Semin Neurol. 2019 Aug;39(4):428-439. doi: 10.1055/s-0039-1687841. Epub 2019 Sep 18. Semin Neurol. 2019. PMID: 31533183 Review.
There are three main groups of prion diseases, termed sporadic (Creutzfeldt-Jakob disease [CJD], sporadic fatal insomnia, and variably protease-sensitive prionopathy), genetic (genetic CJD, fatal familial insomnia, and Gerstmann-Straussler-Scheinker syndro
There are three main groups of prion diseases, termed sporadic (Creutzfeldt-Jakob disease [CJD], sporadic fatal insomni …
Creutzfeldt-Jakob disease and other prion diseases.
Zerr I, Ladogana A, Mead S, Hermann P, Forloni G, Appleby BS. Zerr I, et al. Nat Rev Dis Primers. 2024 Feb 29;10(1):14. doi: 10.1038/s41572-024-00497-y. Nat Rev Dis Primers. 2024. PMID: 38424082 Review.
Human to human transmission of these diseases has occurred due to iatrogenic exposure, and zoonotic forms of prion diseases are linked to bovine disease. Significant progress has been made in the diagnosis of these disorders. Clinical tools for diagnosis comprise brain ima …
Human to human transmission of these diseases has occurred due to iatrogenic exposure, and zoonotic forms of prion diseases are linked to bo …
EEG in Creutzfeldt-Jakob disease.
Wieser HG, Schindler K, Zumsteg D. Wieser HG, et al. Clin Neurophysiol. 2006 May;117(5):935-51. doi: 10.1016/j.clinph.2005.12.007. Epub 2006 Jan 25. Clin Neurophysiol. 2006. PMID: 16442343 Review.
Electroecenphalography (EEG) is an integral part of the diagnostic process in patients with Creutzfeldt-Jakob disease (CJD). The EEG has therefore been included in the World Health Organisation diagnostic classification criteria of CJD. In sporadic CJD (sCJD) …
Electroecenphalography (EEG) is an integral part of the diagnostic process in patients with Creutzfeldt-Jakob disease ( …
Human prion diseases: An overview.
Piñar-Morales R, Barrero-Hernández F, Aliaga-Martínez L. Piñar-Morales R, et al. Med Clin (Barc). 2023 Jun 23;160(12):554-560. doi: 10.1016/j.medcli.2023.03.001. Epub 2023 Apr 21. Med Clin (Barc). 2023. PMID: 37088611 Review. English, Spanish.
Prion diseases are a group of neurodegenerative diseases. The disease-causing agent is a protein (PrP), that is normally produced in the nervous system, aggregated in an abnormal form. ...
Prion diseases are a group of neurodegenerative diseases. The disease-causing agent is a protein (PrP), that is normally produced in …
Creutzfeldt-Jakob disease.
Iwasaki Y. Iwasaki Y. Neuropathology. 2017 Apr;37(2):174-188. doi: 10.1111/neup.12355. Epub 2016 Dec 28. Neuropathology. 2017. PMID: 28028861 Review.
This review will explore the clinical and pathological findings of the various forms of Creutzfeldt-Jakob disease (CJD). Clinical findings of CJD are characterized by rapidly progressive cognitive dysfunction, diffusion-weighted magnetic resonance imaging (DW …
This review will explore the clinical and pathological findings of the various forms of Creutzfeldt-Jakob disease (CJD) …
Creutzfeldt-Jakob disease and ENT.
Sethi N, Kane J, Condon L. Sethi N, et al. J Laryngol Otol. 2013 Nov;127(11):1050-5. doi: 10.1017/S002221511300234X. Epub 2013 Oct 22. J Laryngol Otol. 2013. PMID: 24148284 Review.
OBJECTIVE: This review addresses Creutzfeldt-Jakob disease in the context of ENT, and aims to summarise the relevant history, pathophysiology and implications for contemporary practice. OVERVIEW: Creutzfeldt-Jakob disease is a rare, fatal …
OBJECTIVE: This review addresses Creutzfeldt-Jakob disease in the context of ENT, and aims to summarise the relevant hi …
Creutzfeldt-Jakob disease.
de Villemeur TB. de Villemeur TB. Handb Clin Neurol. 2013;112:1191-3. doi: 10.1016/B978-0-444-52910-7.00040-4. Handb Clin Neurol. 2013. PMID: 23622328 Review.
Three types are known: kuru, variant Creutzfeldt-Jakob disease (CJD), and iatrogenic CJD. All three affect children and young adults, and are transmitted by infectious contamination. ...The disease appears after 4-30 years of incubation. The initial sy …
Three types are known: kuru, variant Creutzfeldt-Jakob disease (CJD), and iatrogenic CJD. All three affect children and …
Creutzfeldt-Jakob disease.
Sikorska B, Knight R, Ironside JW, Liberski PP. Sikorska B, et al. Adv Exp Med Biol. 2012;724:76-90. doi: 10.1007/978-1-4614-0653-2_6. Adv Exp Med Biol. 2012. PMID: 22411235 Review.
Creutzfeldt-Jakob disease (CJD), a neurodegenerative disorder that is the commonest form of human prion disease or transmissible spongiform encephalopathies (TSEs). ...The combination of PrP(Sc) peptide (either 21 kDa or 19 kDa) and the status of the c
Creutzfeldt-Jakob disease (CJD), a neurodegenerative disorder that is the commonest form of human prion disease
Creutzfeldt-Jakob disease and blood transfusion safety.
Seed CR, Hewitt PE, Dodd RY, Houston F, Cervenakova L. Seed CR, et al. Vox Sang. 2018 Apr;113(3):220-231. doi: 10.1111/vox.12631. Epub 2018 Jan 22. Vox Sang. 2018. PMID: 29359329 Free article. Review.
Transmissible spongiform encephalopathies (TSEs) are untreatable, fatal neurologic diseases affecting mammals. Human disease forms include sporadic, familial and acquired Creutzfeldt-Jakob disease (CJD). ...The initial outbreak of vCJD appears to be ov …
Transmissible spongiform encephalopathies (TSEs) are untreatable, fatal neurologic diseases affecting mammals. Human disease forms in …
1,619 results