Results 101 to 110 of about 6,976 (171)

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

Investigating the clinical correlation between sporadic Creutzfeldt Jakob disease and presence of other neurodegenerative pathologies [PDF]

INTRODUCTION: Sporadic Creutzfeldt Jakob Disease (sCJD) is a rapidly progressive and fatal neurodegenerative disorder. Age-specific mortality rates for sCJD have increased up to 65-79 years over the past four decades. Of interest is an apparent reduced
Lumsden, Jane Rebecca
core   +1 more source

Report of the Working Group `Overall Blood Supply Strategy with Regard to Variant Creutzfeldt-Jakob Disease (vCJD)' [PDF]

, 2009
von Koenig, Carl-Heinz Wirsing, Seitz, Rainer, Schlenkrich, Uwe, Gröner, Albrecht, Zerr, Inga, von Dewitz, Christian, Kretzschmar, Hans A., Bluemel, Johannes, Groener, Albrecht, Beekes, Michael, Strobel, Johanna, Heiden, Margarethe, Nuebling, Micha, Willkommen, Hannelore, Dewitz, Christian von, Blümel, Johannes, Burger, Reinhard, Kretzschmar, Hans, Wirsing von König, Carl-Heinz, Schottstedt, Volkmar   +19 more
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

Chorea in Sporadic Creutzfeldt-Jakob Disease [PDF]

Journal of Movement Disorders, 2018
Ai Huey Tan, Tsun Haw Toh, Soon Chai Low, Si Lei Fong, Kah Kian Chong, Kee Wei Lee, Khean Jin Goh, Shen-Yang Lim   +7 more
doaj   +1 more source

Evidence for sporadic Creutzfeldt-Jakob disease being an acquired disease [PDF]

, 2019
Sporadic Creutzfeldt-Jakob Disease (sCJD) is the most common form of human prion disease. It is a rapidly progressive dementia with other associated neurological abnormalities which is invariably fatal, usually within 4-6 months of first symptoms, and
Urwin, Patrick James Michael
core  

Development of a sensitive cell culture system to assess prion infectivity and the efficacy of prion decontamination technologies

, 2012
Creutzfeldt-Jakob disease (CJD) can be iatrogenically transmitted during transplants, grafts and transfusions from CJD infected donors and also contaminated surgical instruments.
Secker, Thomas
core  

Diffusion MR imaging in sporadic Creutzfeldt-Jakob disease

Çukurova Üniversitesi Tıp Fakültesi Dergisi, 2014
Creutzfeldt-Jakob disease (CJD) is a rare dementing disease and is thought to caused by a prion. It is characterized by rapidly progressive dementia, ataxia, myoclonus, akinetic mutism and eventual death.
Burcak Cakir Pekoz, Ozlem Alkan, Semih Giray, senay Demir, Naime Altinkaya   +4 more
doaj  

When Thiamine Is Not the Answer: Sporadic Creutzfeldt-Jakob Disease Mimicking Wernicke's Encephalopathy. [PDF]

Cureus
Fagundo C, Xu C, Loreto R, Abugrara H.
europepmc   +1 more source

Neuropsychiatric symptoms in sporadic Creutzfeldt-Jakob disease. [PDF]

Brain
Zitser J, Forner S, Wong K, Chengshi J, Neuhaus J, Martindale J, Raudabaugh BJ, Benisano K, Goodman-O'Leary K, Metcalf S, Kim MO, Hakimi M, Allen IE, Miller BL, Rosen HJ, Rankin KP, Geschwind MD.   +16 more
europepmc   +1 more source