scholarly journals Creutzfeldt-Jakob disease, Spongiform encephalopathy, Prion disease, diffusion weighted MRI

2006 ◽  
Vol 16 (4) ◽  
pp. 695 ◽  
Author(s):  
AK Gupta ◽  
JK Shah
2001 ◽  
Vol 184 (2) ◽  
pp. 163-167 ◽  
Author(s):  
R. Nitrini ◽  
R.A. Mendonça ◽  
N. Huang ◽  
A. LeBlanc ◽  
J.A. Livramento ◽  
...  

Viruses ◽  
2019 ◽  
Vol 11 (3) ◽  
pp. 232 ◽  
Author(s):  
Paweł Liberski ◽  
Agata Gajos ◽  
Beata Sikorska ◽  
Shirley Lindenbaum

Kuru, the first human prion disease was transmitted to chimpanzees by D. Carleton Gajdusek (1923–2008). In this review, we summarize the history of this seminal discovery, its anthropological background, epidemiology, clinical picture, neuropathology, and molecular genetics. We provide descriptions of electron microscopy and confocal microscopy of kuru amyloid plaques retrieved from a paraffin-embedded block of an old kuru case, named Kupenota. The discovery of kuru opened new vistas of human medicine and was pivotal in the subsequent transmission of Creutzfeldt–Jakob disease, as well as the relevance that bovine spongiform encephalopathy had for transmission to humans. The transmission of kuru was one of the greatest contributions to biomedical sciences of the 20th century.


Neurology ◽  
2016 ◽  
Vol 87 (8) ◽  
pp. 843-845 ◽  
Author(s):  
Keisuke Suzuki ◽  
Akiko Kawasaki ◽  
Takahide Nagashima ◽  
Koichi Hirata

Neurology ◽  
1999 ◽  
Vol 52 (1) ◽  
pp. 205-205 ◽  
Author(s):  
P. Demaerel ◽  
L. Heiner ◽  
W. Robberecht ◽  
R. Sciot ◽  
G. Wilms

2007 ◽  
Vol 24 (3) ◽  
pp. 207-212 ◽  
Author(s):  
Katsuya Satoh ◽  
Susumu Shirabe ◽  
Akira Tsujino ◽  
Hiroto Eguchi ◽  
Masakatsu Motomura ◽  
...  

2006 ◽  
Vol 19 (3) ◽  
pp. 297-300
Author(s):  
S. Purkayastha ◽  
A.K. Gupta ◽  
N.K. Bodhey

2005 ◽  
Vol 4 (10) ◽  
pp. 273-278
Author(s):  
Steve Dealler

Steve Dealler is a medical microbiologist with Morecambe Bay Hospitals NHS Trust. His work on on the diagnosis, epidemiology and potential treatment of transmissible spongiform encephalopathies has brought him inter-national recognition. He has been at the forefront of work on the epidemiology of human food containing the vector for bovine spongiform encephalopathy (BSE), and the development of prophylaxis against variant Creutzfeldt-Jakob disease (vCJD). He is currently working on a potential treatment, pentosan polysulphate. Here he describes the current state of knowledge in the battle against this devastating disease and the political inertia that frustrated earlier attempts to prevent the epidemic.


2020 ◽  
Vol 2 (1) ◽  
Author(s):  
Benjamin Freeze ◽  
Pedro Maia ◽  
Sneha Pandya ◽  
Ashish Raj

Abstract Sporadic Creutzfeldt–Jakob disease is a rare fatal rapidly progressive dementia caused by the accumulation and spread of pathologically misfolded prions. Evidence from animal models and in vitro experiments suggests that prion pathology propagates along neural connectivity pathways, with the transmission of misfolded prions initiating a corruptive templating process in newly encountered brain regions. Although particular regional patterns of disease have been recognized in humans, the underlying mechanistic basis of these patterns remains poorly understood. Here, we demonstrate that the spatial pattern of disease derived from publicly available human diffusion-weighted MRI data demonstrates stereotypical features across patient cohorts and can be largely explained by intrinsic connectivity properties of the human structural brain network. Regional diffusion-weighted MRI signal abnormalities are predicted by graph theoretical measures of centrality, with highly affected regions such as cingulate gyrus demonstrating strong structural connectivity to other brain regions. We employ network diffusion modelling to demonstrate that the spatial pattern of disease can be predicted by a diffusion process originating from a single regional pathology seed and operating on the structural connectome. The most likely seeds correspond to the most highly affected brain regions, suggesting that pathological prions could originate in a single brain region and spread throughout the brain to produce the regional distribution of pathology observed on MRI. Further investigation of top seed regions and associated connectivity pathways may be a useful strategy for developing therapeutic approaches.


Neurology ◽  
1999 ◽  
Vol 52 (7) ◽  
pp. 1514-1514 ◽  
Author(s):  
A. S. Yee ◽  
J. H. Simon ◽  
C. A. Anderson ◽  
C.-I. Sze ◽  
C. M. Filley

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