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Page 1
Creutzfeldt Jakob Disease.
Sitammagari KK, Masood W. Sitammagari KK, et al. 2020 Apr 5. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2021 Jan–. StatPearls. 2021 Jan–. PMID: 29939637 Free Books & Documents. Review.
Creutzfeldt-Jakob disease (CJD) is a rapidly progressive, rare, transmissible, universally fatal, neurodegenerative condition caused by prion proteins. This condition was first described in 1920 by Hans Creutzfeldt, later described in 1921 and 1923 by Alfons Jako
Creutzfeldt-Jakob disease (CJD) is a rapidly progressive, rare, transmissible, universally fatal, neurodegenerative condition caused …
EAACI guidelines on allergen immunotherapy: Hymenoptera venom allergy.
Sturm GJ, Varga EM, Roberts G, Mosbech H, Bilò MB, Akdis CA, Antolín-Amérigo D, Cichocka-Jarosz E, Gawlik R, Jakob T, Kosnik M, Lange J, Mingomataj E, Mitsias DI, Ollert M, Oude Elberink JNG, Pfaar O, Pitsios C, Pravettoni V, Ruëff F, Sin BA, Agache I, Angier E, Arasi S, Calderón MA, Fernandez-Rivas M, Halken S, Jutel M, Lau S, Pajno GB, van Ree R, Ryan D, Spranger O, van Wijk RG, Dhami S, Zaman H, Sheikh A, Muraro A. Sturm GJ, et al. Allergy. 2018 Apr;73(4):744-764. doi: 10.1111/all.13262. Epub 2017 Dec 5. Allergy. 2018. PMID: 28748641
Patients should carry an emergency kit containing an adrenaline autoinjector, H(1) -antihistamines, and corticosteroids depending on the severity of their previous sting reaction(s). The only treatment to prevent further systemic sting reactions is venom immunotherapy. Thi …
Patients should carry an emergency kit containing an adrenaline autoinjector, H(1) -antihistamines, and corticosteroids depending on the sev …
Regulation and Role of Fungal Secondary Metabolites.
Macheleidt J, Mattern DJ, Fischer J, Netzker T, Weber J, Schroeckh V, Valiante V, Brakhage AA. Macheleidt J, et al. Annu Rev Genet. 2016 Nov 23;50:371-392. doi: 10.1146/annurev-genet-120215-035203. Epub 2016 Oct 5. Annu Rev Genet. 2016. PMID: 27732794 Review.
From Creutzfeldt-Jakob disease to the mad cow epidemic.
Sternbach G, Dibble CL, Varon J. Sternbach G, et al. J Emerg Med. 1997 Sep-Oct;15(5):701-5. doi: 10.1016/s0736-4679(97)00152-2. J Emerg Med. 1997. PMID: 9348063
Hans-Gerhard Creutzfeldt and Alfons Jakob independently authored clinical and pathologic descriptions of a new syndrome in the 1920s. ...Because there are sporadic, familial, and iatrogenic forms of Creutzfeldt-Jakob disease, it is considered to have both gen
Hans-Gerhard Creutzfeldt and Alfons Jakob independently authored clinical and pathologic descriptions of a new syndrome in the
Latrogenic Creutzfeldt-Jakob disease with florid plaques.
Kretzschmar HA, Sethi S, Földvári Z, Windl O, Querner V, Zerr I, Poser S. Kretzschmar HA, et al. Brain Pathol. 2003 Jul;13(3):245-9. doi: 10.1111/j.1750-3639.2003.tb00025.x. Brain Pathol. 2003. PMID: 12946015 Review.
Florid plaques indistinguishable from those found in vCJD were identified at a postmortem examination in the brain of a 58-year-old clinical suspect case of Creutzfeldt-Jakob disease (CJD). Western blotting of brain tissue revealed an unusual prion protein type. ...
Florid plaques indistinguishable from those found in vCJD were identified at a postmortem examination in the brain of a 58-year-old clinical …
Prion disease: a tale of folds and strains.
Kretzschmar H, Tatzelt J. Kretzschmar H, et al. Brain Pathol. 2013 May;23(3):321-32. doi: 10.1111/bpa.12045. Brain Pathol. 2013. PMID: 23587138 Review.
Second, human prion diseases have true equivalents in animals, such as scrapie, which has been the subject of experimental research for many years. Variant Creutzfeldt-Jakob disease (vCJD) is a zoonosis caused by bovine spongiform encephalopathy (BSE) prions. ...
Second, human prion diseases have true equivalents in animals, such as scrapie, which has been the subject of experimental research for many …
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