Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease

2015 ◽  
Vol 35 (4) ◽  
pp. 336-342 ◽  
Author(s):  
Anna S. Berghoff ◽  
Anita Trummert ◽  
Ursula Unterberger ◽  
Thomas Ströbel ◽  
Tibor Hortobágyi ◽  
...  
2015 ◽  
Vol 9 (1) ◽  
pp. 2-8 ◽  
Author(s):  
Roberta Diehl Rodriguez ◽  
Lea Tenenholz Grinberg

Argyrophilic grain disease (AGD) is an under-recognized, distinct, highly frequent sporadic tauopathy, with a prevalence reaching 31.3% in centenarians. The most common AGD manifestation is slowly progressive amnestic mild cognitive impairment, accompanied by a high prevalence of neuropsychiatric symptoms. AGD diagnosis can only be achieved postmortem based on the finding of its three main pathologic features: argyrophilic grains, oligodendrocytic coiled bodies and neuronal pretangles. AGD is frequently seen together with Alzheimer's disease-type pathology or in association with other neurodegenerative diseases. Recent studies suggest that AGD may be a defense mechanism against the spread of other neuropathological entities, particularly Alzheimer's disease. This review aims to provide an in-depth overview of the current understanding on AGD.


Author(s):  
S. J. Kish ◽  
J. J. Gilbert ◽  
L. J. Chang ◽  
L. M. Mirchandani ◽  
K. S. Shannak ◽  
...  

2012 ◽  
Vol 24 (1) ◽  
pp. 246-246

JVDI 23:915–923 (September 2011) In the article entitled “Pseudorabies virus infection in Oklahoma hunting dogs” by Sarah D. Cramer et al., on page 918 in the legend to Figure 2, the legend should refer to an “intranuclear” inclusion body instead of an “intracytoplasmic” inclusion body.


2004 ◽  
Vol 89 (1) ◽  
pp. 179-188 ◽  
Author(s):  
Chris Conrad ◽  
Cintia Vianna ◽  
Christian Schultz ◽  
Dietmar R. Thal ◽  
Estifanos Ghebremedhin ◽  
...  

2004 ◽  
Vol 25 ◽  
pp. S408-S409
Author(s):  
Dietmar R. Thal ◽  
Christian Schultz ◽  
Giovannina Botez ◽  
Mrak E. Robert ◽  
Sue T. Griffin ◽  
...  

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