scholarly journals Presence of Reactive Microglia and Neuroinflammatory Mediators in a Case of Frontotemporal Dementia with P301S Mutation

2011 ◽  
Vol 8 (4) ◽  
pp. 221-229 ◽  
Author(s):  
Arianna Bellucci ◽  
Orso Bugiani ◽  
Bernardino Ghetti ◽  
Maria Grazia Spillantini
Keyword(s):  
Frontotemporal Dementia ◽  
Reactive Microglia ◽  
P301s Mutation

A Japanese patient with frontotemporal dementia and parkinsonism by a tau P301S mutation

Neurology ◽  
2000 ◽  
Vol 55 (8) ◽  
pp. 1224-1227 ◽  
Author(s):  
M. Yasuda ◽  
K. Yokoyama ◽  
T. Nakayasu ◽  
Y. Nishimura ◽  
M. Matsui ◽  
...  
Keyword(s):  
Frontotemporal Dementia ◽  
Japanese Patient ◽  
P301s Mutation

scholarly journals Frontotemporal Dementia and Corticobasal Degeneration in a Family with a P301S Mutation in Tau

1999 ◽  
Vol 58 (6) ◽  
pp. 667-677 ◽  
Author(s):  
Orso Bugiani ◽  
Jill R. Murrell ◽  
Giorgio Giaccone ◽  
Masato Hasegawa ◽  
Giuseppe Ghigo ◽  
...  
Keyword(s):  
Frontotemporal Dementia ◽  
Corticobasal Degeneration ◽  
P301s Mutation

Distinct social-behavioral changes in frontotemporal dementia and early onset Alzheimer's disease

2014 ◽  
Author(s):  
Joseph P. Barsuglia ◽  
Michelle J. Mather ◽  
Hemali V. Panchal ◽  
Aditi Joshi ◽  
Elvira Jimenez ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Frontotemporal Dementia ◽  
Early Onset ◽  
Behavioral Changes ◽  
Early Onset Alzheimer’S Disease

Frequency of common genetic forms of frontotemporal dementia in a Russian cohort of patients

2020 ◽  
pp. 30-32
Author(s):  
Ю.А. Шпилюкова ◽  
Е.Ю. Федотова ◽  
Н.Ю. Абрамычева ◽  
С.Н. Иллариошкин
Keyword(s):  
Frontotemporal Dementia ◽  
Clinical Phenotypes ◽  
Mapt Gene ◽  
First Time

Впервые в российской популяции на когорте пациентов с клиническим диагнозом ЛВД исследована частота встречаемости мутаций в наиболее частых генах, ассоциированных с данным заболеванием. Наибольшая часто мутирующими являются гены C9orf72 и GRN. Реже всего встречаются мутации в гене MAPT, что возможно связано с неравномерным представительством клинических фенотипов в нашей выборке. For the first time in the Russian cohort of FTD patients the frequency of mutations in the most common genes associated with this disease was studied. The most frequently mutating are the genes C9orf72 and GRN. Mutations in the MAPT gene are least likely to occur, which is probably due to the uneven representation of clinical phenotypes in our sample.

Sign in / Sign up

Export Citation Format

Share Document