Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Natalie Cookson"'
Autor:
Maximilian J. Johnston, Ara Darzi, Sonal Arora, Natalie Cookson, Bhavesh H. Patel, Dominic King
Publikováno v:
Journal of Medical Internet Research
Background: Most hospitals use paging systems as the principal communication system, despite general dissatisfaction by end users. To this end, we developed an app-based communication system (called Hark) to facilitate and improve the quality of inte
Publikováno v:
Brain Pathol
Scopus-Elsevier
Scopus-Elsevier
Argyrophilic grain disease (AGD) is a recently recognized disorder whose relationship to dementia as well as genetic or biochemical features remain incompletely characterized in part due to diagnostic difficulties engendered by concomitant pathologie
Publikováno v:
Neuropathology and Applied Neurobiology. 29:503-510
Olfactory dysfunction increases with disease severity in Alzheimer's disease (AD), is early and independent of disease severity in Parkinson's disease (PD), but is absent in progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD). Pr
Publikováno v:
Scopus-Elsevier
Objective: To assess demographic and genetic determinants of Alzheimer type pathology in progressive supranuclear palsy (PSP). Methods : From a total of 173 pathologically proven cases of PSP in the Society for PSP Brain Bank, 143 patients (mean age
Autor:
Li Wen Ko, Peter Davies, Takashi Ishizawa, Natalie Cookson, Marisol Espinoza, Dennis W. Dickson
Publikováno v:
Scopus-Elsevier
The CA2 sector of the hippocampus is relatively resistant to neurofibrillary tangles in aging and Alzheimer disease; however, some cases have selective neurofibrillary degeneration in CA2 with sparing of the more vulnerable CA1 sector. Cases such as
Autor:
Nobuo Miyashita, Midori Anno, Dennis W. Dickson, Natalie Cookson, Yasuyuki Okuma, Hideo Mori, Ryota Tanaka, Yoshikuni Mizuno, Tomonori Kobayashi, Yoshio Tsuboi, Yumiko Motoi, Hirotaro Narabayashi
Publikováno v:
Journal of Neurology. 249:669-675
Association between clinical characteristics and types of the tau gene mutation has been observed in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). P301L mutation seldom causes parkinsonism as a leading symptom; instead i
Autor:
Jennifer Adamson, Natalie Cookson, Mike Hutton, Matt Baker, Dennis W. Dickson, Shu Hui Yen, Wan Kyng Liu, Tien V. Le, John Hardy
Publikováno v:
Annals of neurology. 50(4)
Two extended haplotypes of the tau gene (H1 and H2) have been described. The frequency of H1 haplotype is increased in progressive supranuclear palsy (PSP). PSP is associated with filamentous tau lesions in neurons and glia, which are reportedly comp
Publikováno v:
Archives of Neurology. 61:1579
To determine if apolipoprotein E epsilon 4 influences the frequency of Alzheimer-type pathologic features in tauopathies, synucleinopathies, and frontotemporal degeneration and to determine if the frequency of Alzheimer-type pathologic features in sy
Publikováno v:
Archives of Neurology. 59:1597
Background Clinical features suggesting a diagnosis of progressive supranuclear palsy (PSP) include early falls, axial rigidity, vertical supranuclear ophthalmoplegia, and levodopa unresponsiveness. When these clinical features are present, the diagn
Autor:
Shu Hui Yen, Takashi Ishizawa, Dennis W. Dickson, Takashi Togo, Natalie Cookson, Andrew J. Lees, Rohan de Silva, Mike Hutton, Naruhiko Sahara
Publikováno v:
Scopus-Elsevier
Argyrophilic grain disease (AGD) was first reported as an adult-onset dementia, but recent studies have emphasized personality change, emotional imbalance, and memory problems as clinical features of AGD. AGD is characterized by spindle- or comma-sha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::459f01402e732ee992aacb31650ff872
http://www.scopus.com/inward/record.url?eid=2-s2.0-0036269863&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0036269863&partnerID=MN8TOARS