Results 181 to 190 of about 11,518 (218)

Dysarthria as a Presenting Symptom With Rapidly Progressive Imaging Features in Sporadic Creutzfeldt-Jakob Disease: A Case Report. [PDF]

Cureus
Pan T, Wang S.
europepmc   +1 more source

Multidimensional features of sporadic Creutzfeldt-Jakob disease in the elderly: a case report and systematic review. [PDF]

Front Aging Neurosci
Liao J, Hu W, Chen S, Huang C, Dong S, Chen W, Chen X, Chen L.   +7 more
europepmc   +1 more source

A dividing cell model for stable propagation and curing of bona fide human sporadic Creutzfeldt-Jakob Disease prions

Nihat A, Arora P, Schmidt C, Rayner ML, Linehan J, Brandner S, Mead S, Collinge J, Jat PS.   +8 more
europepmc   +1 more source

Diagnostic and Prognostic Value of Plasma GFAP in Sporadic Creutzfeldt-Jakob Disease in the Clinical Setting of Rapidly Progressive Dementia. [PDF]

Int J Mol Sci
Bentivenga GM, Baiardi S, Mastrangelo A, Zenesini C, Mammana A, Rossi M, Polischi B, Capellari S, Parchi P.   +8 more
europepmc   +1 more source

Sporadic Creutzfeldt-Jakob disease in adults over 80 years: a 10-year review of United Kingdom surveillance. [PDF]

Age Ageing
McDermott EA, Watson N, Tam J, Centola J, Kurucu King H, Mackenzie J, Summers D, Green A, Barria MA, Smith C, Pal S.   +10 more
europepmc   +1 more source

Sporadic Creutzfeldt Jakob disease: Case series in Peru. [PDF]

Colomb Med (Cali)
Espinoza S, Canales D, Calderón C, Diaz D, Barreto-Acevedo E.   +4 more
europepmc   +1 more source

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Sporadic Creutzfeldt-Jakob disease

The American Journal of Emergency Medicine, 2022
Being considered among the most fatal neurological conditions, Creutzfeldt-Jakob disease is a transmissible spongiform encephalopathy characterized by its unknown etiology and rapidly progressive neurodegenerative symptoms that often lead to a mean survival of 6 to 12 months.
Parnia, Salehi, Mark, Clark, Jeffer, Pinzon, Abhijit, Patil   +3 more
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Sporadic Creutzfeldt–Jakob Disease—A Review

International Journal of Neuroscience, 2009
The objective is to study a patient with sporadic Creutzfeldt-Jakob disease (CJD). The patient, a 70-year-old woman with a history spanning over 1 month, with acute onset, progressive abnormal behavior, and cognitive decline with generalized asymmetrical myoclonic jerking, startle phenomenon, and cortical blindness, was referred to the hospital.
Stuti, Sharma, Madhurima, Mukherjee, Vivekananda, Kedage, Manjunatha S, Muttigi, Anjali, Rao, Suryanarayana, Rao   +5 more
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