Midcingulate involvement in progressive supranuclear palsy and tau positive frontotemporal dementia

2012 ◽  
Vol 83 (9) ◽  
pp. 910-915 ◽  
Author(s):  
Wang Zheng Chiu ◽  
Janne M Papma ◽  
Inge de Koning ◽  
Laura Donker Kaat ◽  
Harro Seelaar ◽  
...  
Cortex ◽  
2018 ◽  
Vol 109 ◽  
pp. 272-278 ◽  
Author(s):  
Sara Prioni ◽  
Veronica Redaelli ◽  
Paola Soliveri ◽  
Vincenza Fetoni ◽  
Federica Barocco ◽  
...  

Author(s):  
Shirley H. Wray

discusses the brain’s visual architecture for directing and controlling of eye movements:the striate, frontal and parietal cortical areas; and the eye movements themselves—saccades, smooth pursuit, and vergence. The susceptibility to disorders of these systems is illustrated in four detailed cases that follow disease progression from initial symptoms and signs to diagnosis and treatment. The case studies and video displays include a patient with Pick’s disease (frontotemporal dementia), another with Alzheimer’s dementia, and two examples of rare saccadic syndromes, one a patient with the slow saccade syndrome due to progressive supranuclear palsy and one with selective saccadic palsy following cardiac surgery.


Author(s):  
John R. Hodges

This chapter comprises 16 case histories that illustrate methods of assessment described in the rest of this book and the use of the Addenbrooke’s Cognitive Examination (ACE)-III. Each case begins with a brief history from the patient and observations by the family followed by findings on cognitive examination focusing on the profile shown on the ACE-III, the results of imaging investigations, and a discussion of the diagnosis and its differential, with a final summary of the principal conclusions, indicating whether the services of a neuropsychologist are required or not. The cases present important common conditions (such as mild cognitive impairment, Alzheimer’s disease in the mild and moderate stages, behavioural variant frontotemporal dementia, progressive non-fluent aphasia, semantic dementia, corticobasal degeneration, progressive supranuclear palsy, and Huntington’s disease) as well as interesting neuropsychological syndromes (such as prosopagnosia, amnestic stoke, and transient epileptic amnesia).


2015 ◽  
Vol 262 (4) ◽  
pp. 916-922 ◽  
Author(s):  
Christopher Kobylecki ◽  
Matthew Jones ◽  
Jennifer C. Thompson ◽  
Anna M. Richardson ◽  
David Neary ◽  
...  

2010 ◽  
Vol 81 (4) ◽  
pp. 441-445 ◽  
Author(s):  
W. Z. Chiu ◽  
L D Kaat ◽  
H. Seelaar ◽  
S. M Rosso ◽  
A. J. Boon ◽  
...  

2016 ◽  
Vol 4 (2) ◽  
pp. 76-77 ◽  
Author(s):  
Ichiro Yabe ◽  
Fumihito Nakano ◽  
Shinichi Shirai ◽  
Masaaki Matsushima ◽  
Ikuko Takahashi ◽  
...  

1998 ◽  
Vol 11 (2) ◽  
pp. 107-114 ◽  
Author(s):  
Irene Litvan ◽  
Michael Hutton

Progressive supranuclear palsy (PSP) is, after Parkinson's disease, the most common form of degenerative parkinsonism. Several clinical features are used in the recognition of this disorder as well as in the differentiation from related disorders. Clinical criteria that could increase diagnostic accuracy in research studies are also emphasized. Due to a better understanding of the genetic aspects of PSP, recent studies have suggested that it is a recessive disorder in linkage disequilibrium with the tau (τ) gene, rather than a sporadic disorder. In addition, the recent identification of mutations in the τ gene associated with a similar neurodegenerative condition (frontotemporal dementia and parkinsonism linked to chromosome 17) has further strengthened the argument that τ dysfunction is somehow involved in the pathogenesis of PSP. Nongenetic factors that could trigger or perpetuate the cascade of events leading to neuronal degeneration in PSP are also reviewed.


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