Results 161 to 170 of about 22,988 (222)

The Onset of Creutzfeldt-Jakob Disease After COVID-19: Navigating the Diagnostic Challenges and Clinical Evolution. [PDF]

Case Rep Neurol Med
Burakgazi AZ.
europepmc   +1 more source

Distinct neuronal alterations distinguish two subtypes of sporadic Creutzfeldt-Jakob disease with shared dysfunctional pathways. [PDF]

J Clin Invest
Williams K, Groveman BR, Foliaki ST, Race B, Hay A, Walters RO, Thomas T, Zanusso G, Carroll JA, Haigh CL.   +9 more
europepmc   +1 more source

Case Report: Creutzfeldt-Jakob disease and diagnosis challenges: case report and evidence synthesis. [PDF]

F1000Res
Failoc Rojas VE, Yazawa-Ballena Y, Alvarado-Moreno G, Navarro-Flores A, Alva-Diaz C, Pacheco-Barrios K.   +5 more
europepmc   +1 more source

Rapidly progressive dementia in a middle-aged woman: A case of probable sporadic Creutzfeldt-Jakob disease. [PDF]

Med Int (Lond)
Jarquín-Rios VR, Rodríguez-Gutierrez WS, Daberkow-Sánchez E, Flores-Garcia DA, Sánchez Vázquez AT.   +4 more
europepmc   +1 more source

An unusual association between HIV and Creutzfeldt-Jakob disease in a patient from northeastern Brazil. [PDF]

Braz J Infect Dis
Tavares-Júnior JWL, Basílio FJ, Abreu FEB, Tomaz Dos Santos LR, Coimbra PPA, de Arruda ÉAG.   +5 more
europepmc   +1 more source

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Creutzfeldt-Jakob Disease

Neurologic Clinics, 1986
There has been significant advance in our understanding of CJD and similar spongiform encephalopathies in recent years. The range in clinical expression of the disease is better appreciated, and the existence of "atypical" cases of CJD is increasingly recognized.
Z, Davanipour, M, Alter, E, Sobel
openaire   +2 more sources

Creutzfeldt–Jakob disease

Neuropathology, 2000
It is valuable to summarize the milestone study of prion diseases done in Japan for review in the journal Neuropathology in 2000. Many studies done in Japan promote world prion research activity, and also influence further research projects in other groups abroad.
openaire   +4 more sources