Results 101 to 110 of about 5,425,074 (170)

Cortical restricted diffusion as the predominant MRI finding in sporadic Creutzfeldt-Jakob disease

, 2011
Creutzfeldt-Jakob disease is a rare and fatal neurodegenerative disorder with MR findings predominantly limited to the grey matter of the cortex and the basal ganglia.
Ronald J Sattenberg, Brian M Plato, John Parker, Jens O Heidenreich, Sabrina D Talbott   +4 more
core   +1 more source

Detection of Creutzfeldt-Jakob disease prions in skin: implications for healthcare

Genome Medicine, 2018
Editorial summary Evidence has recently been reported of prion seeding activity in skin tissue from patients with sporadic Creutzfeldt-Jakob disease (sCJD). This is relevant information for infection control measures during surgery.
Akin Nihat, Simon Mead
doaj   +1 more source

Decontamination of prions, prion-associated amyloid and inefectivity from surgical stainless steel - implications for the risk of iatrogenic transmission of CJD

, 2009
The physicochemical nature of the infectious agent in prion diseases creates asignificant challenge for decontamination services. It has been shown to be both resistant tostandard methods of decontamination, used to inactivate viruses and bacteria, and ...
Howlin, Robert
core   +1 more source

Spatial Epidemiology of Sporadic Creutzfeldt-Jakob Disease in Apulia, Italy

, 2019
Sporadic Creutzfeldt-Jakob disease (CJD) is a rare neurodegenerative disease caused by prions that is randomly distributed in all countries, with an overall yearly mortality rate of about 1-2 cases per million people.
Capellari, Sabina, Puopolo, Maria, Fedele, Alberto, Biggeri, Annibale, Tiple, Dorina, Sanguedolce, Antonio, Turco, Giuseppa Lucia, Aprile, Valerio, Pocchiari, Maurizio, Colaizzo, Elisa, Ladogana, Anna, Parchi, Piero, Catelan, Dolores, Vaianella, Luana   +13 more
core   +1 more source

Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease [PDF]

, 2017
Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroencephalogram and cerebrospinal fluid biomarkers have been reported to support clinical diagnosis but with variable utility according to subtype.
Taratuto, A., Meissner, B., Brandel, J. P., Varges, D., Smith, P., Romero, C., Collie, D., Begue, C., Summers, D. M., Pocchiari, M., Collins, S. J., Ladogana, A., Will, R. G., Haik, S., Heinemann, U., Zerr, I., Breithaupt, M., Hewer, E., Roberts, H., van Duijn, C., Jansen, Gerard H., Kallenberg, K., Sanchez-Juan, P., Schuur, M., Cras, P., Stokin, G. B., Pimentel, J.   +26 more
core  

Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: U.K. cases 1991-2002

, 2004
Human prion diseases can occur as an idiopathic disorder (sporadic Creutzfeldt–Jakob disease) or can be acquired, as is the case for variant Creutzfeldt–Jakob disease.
MacKenzie, Jan, McCardle, Linda, Knight, Richard, McKimmie, Clive S., McLoughlin, Victoria, Bunn, Tristan J. R., Head, Mark W., Bishop, Matthew T., Williams, Michelle C., Will, Robert G., Lowrie, Suzanne, Ironside, James W.   +11 more
core   +1 more source

Serial EEG findings in sporadic and iatrogenic Creutzfeldt-Jakob disease.

, 2004
OBJECTIVE To study temporal and spatial development of EEG patterns in sporadic and iatrogenic Creutzfeldt-Jakob disease patients. METHODS Temporal and spatial development of EEG patterns in 4 patients with sporadic Creutzfeldt-Jakob disease and 2 ...
Wieser HG, Blättler T, Sitzler M, Schwarz U, Stoeck K, Glatzel M, Bernoulli C   +6 more
core   +1 more source

Autoantibodies in sporadic Creutzfeldt-Jakob disease.

, 2016
IMPORTANCE: The diagnosis of autoimmune and neurodegenerative conditions can be unclear. Treatments such as removing the associated tumor, if present, and immunosuppression can halt or often reverse the progression of autoimmune conditions, but there is ...

core   +1 more source

ePoster

European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source

ePosters Virtual

European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source