NACP/α-Synuclein, NAC, and β-amyloid pathology of familial Alzheimer's disease with the E184D presenilin-1 mutation: a clinicopathological study of two autopsy cases

2002 ◽  
Vol 104 (6) ◽  
pp. 637-648 ◽  
Author(s):  
Osamu Yokota ◽  
Seishi Terada ◽  
Hideki Ishizu ◽  
Hiroshi Ujike ◽  
Takeshi Ishihara ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Presenilin 1 ◽  
Familial Alzheimer’S Disease ◽  
Amyloid Pathology ◽  
Clinicopathological Study ◽  
Presenilin 1 Mutation ◽  
Β Amyloid ◽  
Familial Alzheimer's Disease

Presenilin-1 mutation E318G and familial Alzheimer's disease in the Italian population

2007 ◽  
Vol 28 (11) ◽  
pp. 1682-1688 ◽  
Author(s):  
Diego Albani ◽  
Ignazio Roiter ◽  
Vladimiro Artuso ◽  
Sara Batelli ◽  
Francesca Prato ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Presenilin 1 ◽  
Italian Population ◽  
Familial Alzheimer’S Disease ◽  
Presenilin 1 Mutation ◽  
Familial Alzheimer's Disease

A novel presenilin 1 mutation (L282F) in familial Alzheimer’s disease

2009 ◽  
Vol 256 (9) ◽  
pp. 1575-1577 ◽  
Author(s):  
Tsuyoshi Hamaguchi ◽  
Akiyoshi Morinaga ◽  
Tamao Tsukie ◽  
Ryozo Kuwano ◽  
Masahito Yamada
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Presenilin 1 ◽  
Familial Alzheimer’S Disease ◽  
Presenilin 1 Mutation ◽  
Familial Alzheimer's Disease

Early-onset familial Alzheimer’s disease related to presenilin 1 mutation resembling autosomal dominant spinocerebellar ataxia

2013 ◽  
Vol 260 (4) ◽  
pp. 1177-1179 ◽  
Author(s):  
Pedro Braga-Neto ◽  
José Luiz Pedroso ◽  
Helena Alessi ◽  
Paulo Victor Sgobbi de Souza ◽  
Paulo Henrique Ferreira Bertolucci ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Spinocerebellar Ataxia ◽  
Early Onset ◽  
Autosomal Dominant ◽  
Presenilin 1 ◽  
Familial Alzheimer’S Disease ◽  
Presenilin 1 Mutation ◽  
Familial Alzheimer's Disease ◽  
Autosomal Dominant Spinocerebellar Ataxia

Early psychiatrics symptoms in familial Alzheimer’s disease with presenilin 1 mutation (I83T)

2015 ◽  
Vol 123 (4) ◽  
pp. 451-453 ◽  
Author(s):  
Saloua Fray ◽  
Nadia Ben Ali ◽  
Afef Achouri Rassas ◽  
Meriem Kechaou ◽  
Nouria Oudiaa ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Presenilin 1 ◽  
Familial Alzheimer’S Disease ◽  
Presenilin 1 Mutation ◽  
Familial Alzheimer's Disease

P3-224: Clinical phenotype of familial Alzheimer's disease caused by the H163R presenilin 1 mutation

2008 ◽  
Vol 4 ◽  
pp. T586-T586
Author(s):  
Estrella Gómez-Tortosa ◽  
Sagrario Manzano ◽  
David G. Muñoz ◽  
M. José Sainz ◽  
Adolfo Jiménez-Huete ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Clinical Phenotype ◽  
Presenilin 1 ◽  
Familial Alzheimer’S Disease ◽  
Presenilin 1 Mutation ◽  
Familial Alzheimer's Disease
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