Results 71 to 80 of about 5,030,757 (219)
Application of real-time quaking-induced conversion in Creutzfeldt–Jakob disease surveillance
, 2023 Background Evaluation of the application of CSF real-time quaking-induced conversion in Creutzfeldt–Jakob disease surveillance to investigate test accuracy, influencing factors, and associations with disease incidence.
Hermann, Peter +10 more
core +1 more source
Probable sporadic Creutzfeldt–Jakob disease mimicking focal epilepsy
Epilepsy and Behavior Case Reports, 2019 Creutzfeldt–Jakob disease (CJD) presents with seizures as an early symptom in only approximately 3% of cases. These seizures often present as nonconvulsive status epilepticus (NCSE) or epilepsia partialis continua (EPC).
Pei-Shan Hsiao +5 more
doaj +1 more source
Creutzfeldt-Jakob disease in Sweden [PDF]
Journal of Neurology, Neurosurgery & Psychiatry, 1998 To find and investigate, retrospectively, as many cases as possible of Creutzfeldt-Jakob disease (CJD) in Sweden dying during the period 1 January 1985 to 31 December 1996 and to detect any possible case(s) of new variant CJD.The patients were found through computer search of all death certificates in Sweden on which CJD was mentioned, through ...
openaire +2 more sources
Diagnosing Creutzfeldt-Jakob disease [PDF]
BMJ, 1996 Case identification depends on neurological and neuropathological assessment Central to the identification and classification of patients with Creutzfeldt-Jakob disease (CJD) is the application of standardised diagnostic criteria based on accumulated data on the clinical and pathological features of the disease.
R, Will, M, Zeidler
openaire +2 more sources
Modeling localized deer removal strategies for managing chronic wasting disease
The Journal of Wildlife Management, Volume 90, Issue 7, September 2026.We used an agent‐based model developed for chronic wasting disease (CWD) in Midwestern white‐tailed deer to assess localized deer removal strategies and how local conditions affect management outcomes. Parcel‐based and ring culling were most effective at reducing CWD prevalence and persistence, and transmission was always greater at greater deer ...
Noelle E. Thompson +5 more
wiley +1 more source
Case series of Creutzfeldt-Jakob disease in a third-level hospital in Quito
, 2018 Background: Creutzfeldt-Jakob disease is a rare and fatal neurodegenerative disorder that affects mammals and humans. The prevalence of this disease in the United States is 0.5 to 1 per million inhabitants.
Serrano Dueñas, Marcos
core +1 more source
Sporadic Creutzfeldt–Jakob Disease
Acta Medica BulgaricaSporadic Creutzfeldt–Jakob disease is a rare and fatal human prion disease characterized by a rapidly progressive dementia, myoclonus, cerebellar, pyramidal, extrapyramidal, visual, and psychiatric symptoms. These findings are all non-specific and making
Zhelyazkova S. +3 more
doaj +1 more source
Case Reports in Neurological Medicine, 2018 Sporadic Creutzfeldt-Jakob disease (sCJD) is a type of progressive, subacute encephalopathy associated with spongiform degeneration of the central nervous system.
Sira Carrasco García de León +3 more
doaj +1 more source
Chitinases in Tear Fluid of Patients With Amyotrophic Lateral Sclerosis
European Journal of Neurology, Volume 33, Issue 9, September 2026.This study investigated chitinase expression in ALS across tear fluid (TF), CSF, and serum. CHI3L1 was elevated in TF, consistent with changes in CSF, but not serum. Furthermore, combining TF chitinases with serum NfL improved diagnostic discrimination.
Lara Wenz +10 more
wiley +1 more source