scholarly journals Progressive supranuclear palsy and primary lateral sclerosis secondary to globular glial tauopathy: a case report and a practical theoretical framework for the clinical prediction of this rare pathological entity

Neurocase ◽  
2020 ◽  
Vol 26 (2) ◽  
pp. 91-97 ◽  
Author(s):  
Andy J. Liu ◽  
Jessica E. Chang ◽  
Georges Naasan ◽  
Adam L. Boxer ◽  
Bruce L. Miller ◽  
...  
2018 ◽  
Vol 33 (2) ◽  
pp. 131-133
Author(s):  
A. Alabajos Cea ◽  
I. Máñez Añón ◽  
C. Roda Alcayde ◽  
J.F. Vázquez Costa ◽  
M. Guevara Salazar

2012 ◽  
Vol 27 (7) ◽  
pp. 903-906 ◽  
Author(s):  
Elizabeth A. Coon ◽  
Jennifer L. Whitwell ◽  
Clifford R. Jack ◽  
Keith A. Josephs

2012 ◽  
Vol 323 (1-2) ◽  
pp. 147-153 ◽  
Author(s):  
Shigeto Nagao ◽  
Osamu Yokota ◽  
Reiko Nanba ◽  
Hiroshi Takata ◽  
Takashi Haraguchi ◽  
...  

2013 ◽  
Vol 329 (1-2) ◽  
pp. 70-71 ◽  
Author(s):  
Shigeto Nagao ◽  
Osamu Yokota ◽  
Chikako Ikeda ◽  
Seishi Terada ◽  
Yuetsu Ihara ◽  
...  

Author(s):  
Konstantin Gulyabin

Mills' syndrome is a rare neurological disorder. Its nosological nature is currently not completely determined. Nevertheless, Mills' syndrome is considered to be a rare variant of the degenerative pathology of the central nervous system – a variant of focal cortical atrophy. The true prevalence of this pathology is unknown, since this condition is more often of a syndrome type, observed in the clinical picture of a number of neurological diseases (primary lateral sclerosis, frontotemporal dementia, etc.) and is less common in isolated form.


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